Sas cdisc sdtm

Hi guys, we offers live web instructor based courses that are available for Statistical Programmer Analysts, Biostatisticians and Data Managers.Our training are in the areas of: CDISC Training, SAS TLF Training, SAS Clinical Programming Training, Clinical Trials Training. contact for details: 9963946766

INSTITUTE OF GOOD CILNICAL PRACTICE (IGCP) GIVE Practical Exposure to Clinical research and Clinical Data Management industry. We are committed to attracting, developing, rewarding and retaining the best people in Clinical Research and Clinical Data management field to Teach conduct and support our innovative and highest quality Knowledge.IGCP-ians Success stories summaries our Reputation,our Promise and our Future as renowned organization for both Clinical Research Domain and Technical Knowledge. • Students placed in MNC’s Worldwide. • Practical training as per the industry requirement. • Training by Subject Matter Experts.(SME) • Only Institute in India to train on CDISC-SDTM. • SAS Projects On Table Listings Figures (TLF’S), SDTM and Data Validation. • 3-4Years Knowledge is guaranteed by the end of the course.

Institute of Good Clinical Practice (iGCP) offers different unique programs for aspiring professionals willing to pursue a career in Clinical Research, Clinical Data Management, CDISC-SDTM, SAS. The training program aims to provide a career path for professionals from Life Sciences and Statistics background. Highly experienced staffs from clinical research and data management industry trains you with hands on experience on various areas in clinical research, Clinical Data Management, CDISC-SDTM, SAS, Pharmacovigilance, Drug regulatory affairs,etc. Institute of Good Clinical Practice (iGCP) provide training in three different modes like Class Room, Online-learning for all Medical, Pharmacy and Science students and professionals aspiring to make a career in Clinical Research.

INSTITUTE OF GOOD CILNICAL PRACTICE (IGCP) GIVE Practical Exposure to Clinical research and Clinical Data Management industry..We are committed to attracting, developing, rewarding and retaining the best people in Clinical Research and Clinical Data management field to Teach conduct and support our innovative and highest quality Knowledge.IGCP-ians Success stories summaries our Reputation, our Promise and our Future as renowned organization for both Clinical Research Domain and Technical Knowledge. • Students placed in MNC’s Worldwide. • Practical training as per the industry requirement. • Training by Subject Matter Experts.(SME) • Only Institute in India to train on CDISC-SDTM. • SAS Projects On Table Listings Figures (TLF’S), SDTM and Data Validation. • Training Clinical Data management on Electronic Data Capture Tool (EDC). • 3-4Years Knowledge is guaranteed by the end of the course. • Internship Programs on Clinical Data Management & SAS Projects. Teaching Mode: Class Room and Online* ADDRESS: INSTITUTE OF GOOD CLINICAL PRACTICE, # 2ND FLOOR,ABOVE MORE SUPER MARKET, NEAR SRIPURAM COLONY BUS STOP, MOOSARAMBAGH, MALAKPET, HYDERABAD. PH:,, 040 .

Institute of Good Clinical Practice (iGCP) offers different unique programs for aspiring professionals willing to pursue a career in Clinical Research, Clinical Data Management,CDISC-SDTM, and SAS. The training program aims to provide a career path for professionals from Life Sciences and Statistics background. Highly experienced staffs from clinical research and data management industry trains studentswith hands on experience on various areas in clinical research, Clinical Data Management, CDISC-SDTM,SAS, Pharmacovigilance,Drug regulatory affairs, Table Listings Figures (TLF’S)etc. Institute of Good Clinical Practice (iGCP) provide training in three different modes like Class Room,Online-learning for all Medical, Pharmacy and Science students and professionals aspiring to make a career in Clinical Research. Technical learning's: Extensive knowledge of drug safety and drug development process and procedures In-depth knowledge of coding principles, submission criteria, regulatory timeline requirements, technical requirements and guidelines Extensive knowledge of US and ICH safety reporting regulations and guidelines. Good understanding of IND safety reports, 21 CFR part 11 and HIPPA guidelines. Performed triage, evaluation and processing of adverse event reports from post marketing and clinical sources in accordance with FDA and ICH guidelines Working knowledge pertaining to MedDRA and WHO Drug dictionaries. Proficient in data entry and excellent knowledge of ARGUS safety database. Eligibility: Bachelor's, Master’s, or PhD, MBBS/ MD/B.D.S /M.D.S/ B.A.M.S / B.H.M.S/B.P.T/ B.Tech (Biotechnology / Pharmaceutical Science) / B. Pharm /M.Pharm /BVSC / B.Sc. (Nursing) / B.Sc./M.Sc, M.Pharmacy, M.Sc /MA (Statistics) and all professionals working with Pharmaceutical companies, CROs and Hospital. MAIL ID: WEBSITE: www.igcp.co.in FOR ONLINE TIMINGS: PM TO PM FOR CLASS ROOM TIMINGS: AM TO PM ADDRESS: INSTITUTE OF GOOD CLINICAL PRACTICE, # 2ND FLOOR,ABOVE MORE SUPER MARKET, NEAR SRIPURAM COLONY BUS STOP, MOOSARAMBAGH, MALAKPET, HYDERABAD. PH:,, 040 .

Clinical SAS Online Training || 91- Hi Guys, Do you want Clinical SAS Online Training? Here is the right place. We will provide the best online trainings in the training Industry on clinical SAS by expert SAS certified and real time experienced trainers with live data and live examples. List of SAS Clinical Courses: 1.Base SAS 2.Advanced SAS 3.Clinical Domain Knowledge 4.Real Time Scenarios 5.CDISC(SDTM & ADaM) 6.Creating Tables, Listings & Graphs(TLGs or TLFs) 7.Roles and Responsibilities of SAS Programmer at different levels 8.How to Validate Data sets & Reports 9.How to Create ADaM Specification 10.Real time Project Work We also offers/provides: Introduction to Clinical trials ISS/ISE tables 21CFR PART II/ICH guidelines  CRF review  Validations and Edit Checks  Info about e-submissions  Knowledge on documentation part in clinical industry.  Assistance for Base SAS and Advance SAS Certification  Clinical Projects with the real data  Assistance to join in the US consultancies for students  Resume preparation  Conduct mock interviews  On job support Special qualities in our training: Experts in Clinical Domain & SAS Certified Programmer Joining the class on time Share the screen Every day 1 hr -1:15 min class (Moday to Friday US timings) Providing the best material Explaining the topics with best examples Showing the real data Showing the real documents Proper guidance about the Clinical Industry real time work Please see my LinkedIn profile for more information: 91- if you any queries or questions. Regards, Ram SaiArundathi online trainings SAS-Clinical Online Classes Ph: 91-

Learn important & required concepts related to clinical sas programming which is a blend of base sas, advance sas & CDISC SDTM standards. Describe the clinical research process (phases, key roles, and key organizations). Describe regulatory requirements (principles of 21 CFR Part 11, International Conference on Harmonization, Good Clinical Practices). Read more:

INSTITUTE OF GOOD CLINICAL PRACTICE (IGCP) GIVE Practical Exposure to Clinical research and Clinical Data Management industry. We are committed to attracting, developing, rewarding and retaining the best people in Clinical Research and Clinical Data management field to Teach conduct and support our innovative and highest quality Knowledge.IGCP-ians Success stories summaries our Reputation,our Promise and our Future as renowned organization for both Clinical Research Domain and Technical Knowledge. • Students placed in MNC’s Worldwide. Practical training as per the industry requirement. • Training by Subject Matter Experts.(SME) • Provides training for CDISC-SDTM and ADaM. • SAS Projects On Table Listings Figures (TLF’S), SDTM and Data Validation. • 2-3Years Knowledge is guaranteed by the end of the course.

To Know more about Clinical Trial Data Management & SAS Clinical Programming and Data Conversion CDISC SDTM Standards! Placement assistance is provided to all the program participants. The Institute is in touch with several reputed Clinical Trial and Pharma companies where passing out students will be placed. The CDS institute has also tied up with several reputed Recruitment Process Outsourcing Contact: Courses Offered 1) Clinical Research 2) Clinical Data Management(EDC Tools) 3) SAS Clinical Programming 4) CDISC(SDTM.ADaM) Phone:

Ram Clinical SAS Online/Corporate Trainer Ph: 91- Hi Guys, Do you want Clinical SAS Online Training? Here is the right place. We will provide the best online trainings in the training Industry on clinical SAS by expert SAS certified and real time experienced trainers with live data and live examples. List of SAS Clinical Courses: 1.Base SAS 2.Advanced SAS 3.Clinical Domain Knowledge 4.Real Time Scenarios 5.CDISC(SDTM & ADaM) 6.Creating Tables, Listings & Graphs(TLGs or TLFs) 7.Roles and Responsibilities of SAS Programmer at different levels 8.How to Validate Data sets & Reports 9.How to Create ADaM Specification 10.Real time Project Work We also offers/provides: Introduction to Clinical trials ISS/ISE tables 21CFR PART II/ICH guidelines  CRF review  Validations and Edit Checks  Info about e-submissions  Knowledge on documentation part in clinical industry.  Assistance for Base SAS and Advance SAS Certification  Clinical Projects with the real data  Assistance to join in the US consultancies for students  Resume preparation  Conduct mock interviews  On job support Special qualities in our training: Experts in Clinical Domain & SAS Certified Programmer Joining the class on time Share the screen Every day 1 hr -1:15 min class (Moday to Friday US timings) Providing the best material Explaining the topics with best examples Showing the real data Showing the real documents Proper guidance about the Clinical Industry real time work Please 91- if you any queries or questions. Regards, Ram SaiArundathi online trainings SAS-Clinical Online Classes Ph: 91-

sasonlinetraining.training Analytics IT Solutions offers a comprehensive portfolio of Global Standard technical training and education services designed for individuals, companies and public organizations to acquire, maintain and optimize their IT skills in programming, Analytics, Business Intelligence Software and other Software’s. Renown Analytics provide exclusively designed course material for all the courses to teach the various IT technology concepts with world class standards Courses Offered: SAS (online Training, Corporate Training) SAS Clinical Proc SQL MACROS STATS CDISC SDTM ADaM TLF’S Other Courses: SAS Clinical 9.3SAS BI, SAS Analytics AS Advanced Analytics, SAS Admin, SAS Solutions JAVA, PHP,.NET, Android, Oracle Highlights of Renown Analytics Centre of Excellence: • Trainings with latest versions (Current SAS 9.3). • Real-Time domain experienced Faculty. • 24/7 Lab facility. • Project Oriented Training to meet MNC Standards. • Continuous Assessment to get into the right track. • Resume Preparation. • Conducting Mock interviews. • Guidance to get SAS Certifications. • Soft Skills Training and Development We will provide more informations visit my site:

IGCP understand the exact requirement of the Contract Research Organization’s (CRO’s) for their need of the trained manpower as we have experience working with them since many years handling their CLINICAL TRIALS, CLINICAL DATA MANAGEMENT, CLINICAL ACQUISITION AND SUBMISSION DATA STANDARDS (CDISC-CDASH,SDTM,ODM), SAS, PHARMACOVIGILANCE etc. With the experience working with CRO’s, we have designed each training module focusing to expose the students practically to each task with logical excercises covering all the areas of Clinical Trials and Clinical Data Management, CDISC-SDTM and SAS. Institute of Good Clinical Practice (iGCP) offers different unique programs for aspiring professionals willing to pursue a career in Clinical Research, Clinical Data Management, CDISC-SDTM, SAS. The training program aims to provide a career path for professionals from Life Sciences and Statistics background. Highly experienced staffs from clinical research and data management industry trains you with hands on experience on various areas in clinical research, Clinical Data Management, CDISC-SDTM, SAS, Pharmacovigilance, Drug regulatory affairs,etc. Institute of Good Clinical Practice (iGCP) provide training in three different modes like Class Room, Online-learning for all Medical, Pharmacy and Science students and professionals aspiring to make a career in Clinical Research. Class Room Training Certificate Program in Clinical Research and Clinical Data Management Certificate Program in Clinical Research, Clinical Data Management and SAS Certificate Program in Clinical Research, Clinical Data Management and SAS with SDTM. Certificate in CDISC-SDTM and SAS Online Training Certificate Program in Clinical Research and Clinical Data Management Certificate Program in Clinical Research, Clinical Data Management and SAS Certificate Program in Clinical Research, Clinical Data Management and SAS with SDTM. Certificate in CDISC-SDTM with SAS Eligibility These programs are most suitable for Life Science Graduates, Doctors, Medical Professionals, and Pharmacists etc. Any one of the following minimum qualifications is mandatory to be eligible: B. Sc. / M. Sc. in Biotechnology, Microbiology, Genetics, Biochemistry or life sciences. M.B.B.S / B.D.S / B.A.M.S / B.H.M.S. B. Pharmacy/ M. Pharmacy Graduates or Post Graduates in Nursing B.E (BT) / B. Tech (BT) Certification ISO Certification Recognized by Ministry of Labour and Employment DGE & T (Students can register in Central Govt Employment Exchange) Recognized by Commissionerate of Employment and Training A.P, Hyderabad (Students can register in State Govt Employment Exchange) Contact details: ADDRESS: INSTITUTE OF GOOD CLINICAL PRACTICE, # 2ND FLOOR,ABOVE MORE SUPER MARKET, NEAR SRIPURAM COLONY BUS STOP, MOOSARAMBAGH, MALAKPET, HYDERABAD. PH:,, 040 .

BASE SAS MODULES Day 1: Introduction to the SAS System Components of Base SAS Software Output Produced by the SAS System Ways to Run SAS Programs Running Programs in the SAS Windowing Environment Introduction to DATA Step Processing The SAS Data Set introduction How the DATA Step Works: A Basic Introduction Supplying Information to Create a SAS Data Set Introduction to Raw Data Examine the Structure of the Raw Data: Factors to Consider Reading Unaligned Data Reading Data That Is Aligned in Columns Reading Data That Requires Special Instructions Reading Unaligned Data with More Flexibility Mixing Styles of Input Day 2: Introduction to Beyond the Basics with Raw Data Using INFILE statement and various options. Testing a Condition before Creating an Observation Creating Multiple Observations from a Single Record Reading Multiple Records to Create a Single Observation Problem Solving: When an Input Record Unexpectedly Does Not have enough values Day 3: Introduction to Starting with SAS Data Sets Understanding the Basics Input SAS Data Set for Examples Reading Selected Observations Reading Selected Variables Creating More Than One Data Set in a Single DATA Step Using the DROP=, KEEP= and WHERE= Data Set Options for Efficiency Introduction to DATA Step Processing Input SAS Data Set for Examples Adding Information to a SAS Data Set Defining Enough Storage Space for Variables Conditionally Deleting an Observation Day 4: Introduction to Working with Numeric Variables About Numeric Variables in SAS Input SAS Data Set for Examples Calculating with Numeric Variables Comparing Numeric Variables Storing Numeric Variables Efficiently Numeric Functions. Day 5: Introduction to Working with Character Variables Input SAS Data Set for Examples Identifying Character Variables and Expressing Character Values Handling Missing Values Creating New Character Values Saving Storage Space by Treating Numbers as Characters Character Functions Day 6: Introduction to Acting on Selected Observations Input SAS Data Set for Examples Selecting Observations Constructing Conditions Comparing Characters Introduction to Creating Subsets of Observations Input SAS Data Set for Examples Selecting Observations for a New SAS Data Set Conditionally Writing Observations to One or More SAS Data Sets Day 7: Introduction to Working with Grouped or Sorted Observations Input SAS Data Set for Examples Working with Grouped Data Working with Sorted Data Introduction to Using More Than One Observation in a Calculation Input File and SAS Data Set for Examples Accumulating a Total for an Entire Data Set Obtaining a Total for Each BY Group Writing to Separate Data Sets Using a Value in a Later Observation Day 8: Introduction to Using More Than One Observation in a Calculation Input File and SAS Data Set for Examples Accumulating a Total for an Entire Data Set Obtaining a Total for Each BY Group Writing to Separate Data Sets Using a Value in a Later Observation Introduction to Working with Dates Understanding How SAS Handles Dates Input File and SAS Data Set for Examples Entering Dates Displaying Dates Using Dates in Calculations Using SAS Date Functions Comparing Durations and SAS Date Values Day 9: Introduction to Combining SAS Data Sets Definition of Concatenating Definition of Interleaving Definition of Merging Definition of Updating Definition of Modifying 237 Comparing Modifying, Merging, and Updating Data Sets Day 10: Introduction to Concatenating SAS Data Sets Concatenating Data Sets with the SET Statement Concatenating Data Sets Using the APPEND Procedure Choosing between the SET Statement and the APPEND Procedure. Introduction to Interleaving SAS Data Sets Understanding BY-Group Processing Concepts Interleaving Data Sets Day 11: Introduction to Merging SAS Data Sets Understanding the MERGE Statement One-to-One Merging Match-Merging Choosing between One-to-One Merging and Match-Merging Introduction to Updating SAS Data Sets Understanding the UPDATE Statement Understanding How to Select BY Variables Updating a Data Set Updating with Incremental Values Understanding the Differences between Updating and Merging Handling Missing Values Day 12: Input SAS Data Set for Examples Modifying a SAS Data Set: The Simplest Case Modifying a Master Data Set with Observations from a Transaction Data Set Understanding How Duplicate BY Variables Affect File Update Handling Missing Values Introduction to Conditional Processing from Multiple SAS Data Sets Input SAS Data Sets for Examples Determining Which Data Set Contributed the Observation Combining Selected Observations from Multiple Data Sets Performing a Calculation Based on the Last Observation Day 13: Introduction to Analysing Your SAS Session with the SAS Log Understanding the SAS Log Locating the SAS Log Understanding the Log Structure Writing to the SAS Log Suppressing Information to the SAS Log Changing the Log’s Appearance Introduction to Directing SAS Output and the SAS Log Input File and SAS Data Set for Examples Routing the Output and the SAS Log with PROC PRINTTO Storing the Output and the SAS Log in the SAS Windowing Environment Redefining the Default Destination in a Batch or Non interactive Environment Introduction to Diagnosing and Avoiding Errors Understanding How the SAS Supervisor Checks a Job Understanding How SAS Processes Errors Distinguishing Types of Errors Diagnosing Errors Using a Quality Control Checklist Day 14: Introduction to Creating Detail and Summary Reports with the REPORT Procedure Understanding How to Construct a Report Input File and SAS Data Set for Examples Creating Simple Reports Creating More Sophisticated Reports Day 15: Introduction to Proc means Deriving descriptive statistics Introduction to Proc univariate and various options Day 16: Introduction to Proc freq Calculating counts using Freq Outputting the counts into a dataset Proc Transpose introduction Using VAR, ID and BY statement efficiently in transpose Reshaping the data with required variables Day 17: Introduction to Producing Charts to Summarize Variables Understanding the Charting Tools Input File and SAS Data Set for Examples Charting Frequencies with the CHART Procedure Customizing Frequency Charts Creating High-Resolution Histograms Day 18: Introduction to Writing Lines to the SAS Log or to an Output File Understanding the PUT Statement Writing Output without Creating a Data Set Writing Simple Text Introduction to the Basics of Understanding and Customizing SAS Output Understanding Output Input SAS Data Set for Examples Locating Procedure Output Making Output Informative Controlling Output Appearance Controlling the Appearance of Pages Representing Missing Values Day 19: Introduction to Customizing SAS Output by Using the Output Delivery System Input Data Set for Examples Understanding ODS Output Formats and Destinations Selecting an Output Format Creating Formatted Output Day 20: Proc Format introduction Creating format catalogue Converting catalogue to dataset Storing formats permanently and finding out formats in a library Accessing a Permanent SAS Data Set with User-Defined Formats ADVANCED SAS MODULES Day 21: Getting Started with the Macro Facility Replacing Text Strings Using Macro Variables Generating SAS Code Using Macros More Advanced Macro Techniques Other Features of the Macro Language Introduction to SAS Programs and Macro Processing How SAS Processes Statements without Macro Activity How SAS Processes Statements with Macro Activity Introduction to Macro Variables Macro Variables Defined by SAS Macro Variables Defined by Users Using Macro Variables Displaying Macro Variable Values Referencing Macro Variables Indirectly Manipulating Macro Variable Values with Macro Functions Introduction to Macro Processing Defining and Calling Macros How the Macro Processor Compiles a Macro Definition How the Macro Processor Executes a Compiled Macro Summary of Macro Processing Day 22: Introduction to the Scopes of Macro Variables Global Macro Variables Local Macro Variables Writing the Contents of Symbol Tables to the SAS Log How Macro Variables Are Assigned and Resolved Introduction to Macro Expressions Defining Arithmetic and Logical Expressions How the Macro Processor Evaluates Arithmetic Expressions Day 23: Introduction to Macro Quoting Deciding When to Use a Macro Quoting Function and Which Function to Use Using Various Macro Functions %STR and %NRSTR Functions etc Using the %BQUOTE and %NRBQUOTE Functions Referring to Already Quoted Variables Deciding How Much Text to Mask with a Macro Quoting Function Using %SUPERQ Summary of Macro Quoting Functions and the Characters They Mask Unquoting Text How Macro Quoting Works Other Functions That Perform Macro Quoting Day 24: Introduction to Storing and Reusing Macros Saving Macros in an Auto call Library Saving Macros Using the Stored Compiled Macro Facility General Macro Debugging Information Troubleshooting Your Macros Debugging Techniques Introduction to Writing Efficient and Portable Macros Keeping Efficiency in Perspective Writing Efficient Macros Writing Portable Macros PROJECT CONTENT COVERED Day Creation of Efficacy tables. Creation of Standard and safety tables. Day 28 Creation of listings Day Creation of Graphs a)Bar Charts b)Scatter plot c)Line plot d)Box plot Day 31 Creation of Analysis datasets/derived datasets Day 32 Introduction to SDTM CRF Annotation (ONLY BASICS) Introduction to mapping specification (ONLY BASICS) Introduction to SDTM dataset Creation (ONLY BASICS) Validation in Open CDISC (ONLY BASICS) Day 33 Introduction to ADAM Standards (ONLY BASICS) Mock interview and providing assistance for interview preparation Contact:

Institute of Good Clinical Practice:- Institute of Good Clinical Practice provides internship for aspiring professionals willing to pursue career in Clinical Research, Clinical Data Management and Data Analytics. The aim of Internship program to provide hands on experience and real time knowledge in Clinical Research, Data management and Analysis. Program Highlights: 6 months of internship program (Case Studies, Theory &Practical, Ongoing SDTM projects) Lectures by Industry experts Assignments and providing Hands on experience. Instititute of good clinical pracice also providing online and class room training. 1.Module I: CRF/DVS/STUDY BUILD Development of Protocol required CRF’ Designing eCRF Data Validation Plan Specification Discrepancy Management SAE and External Data Reconciliation Study Build 2.Module II: CDISC-SDTM Annotation of CRF’s SDTM Mapping Specification Define.XML 3.Module III: SAS SAS programming on Data Validation SAS programming on SDTM mapping Specification SAS Programming on Define SAS Statistical Programming Diploma in Clinical Research & Clinical Data Management. Courses Highlights: Excellent Coaching By Industry Experts. Weekend Assignments & Study Material. Exposure to Live Clinical Trial Projects. Placement Assistance, Mock Interviews & Professional Development. ADDRESS: INSTITUTE OF GOOD CLINICAL PRACTICE, # 2ND FLOOR,ABOVE MORE SUPER MARKET, NEAR SRIPURAM COLONY BUS STOP, MOOSARAMBAGH, MALAKPET, HYDERABAD. PH:,, 040 .

Institute of Good Clinical Practice:- Institute of Good Clinical Practice provides internship for aspiring professionals willing to pursue career in Clinical Research, Clinical Data Management and Data Analytics. The aim of Internship program to provide hands on experience and real time knowledge in Clinical Research, Data management and Analysis. Program Highlights: 6 months of internship program (Case Studies, Theory &Practical, Ongoing SDTM projects) Lectures by Industry experts Assignments and providing Hands on experience. Instititute of good clinical pracice also providing online and class room training. 1.Module I: CRF/DVS/STUDY BUILD Development of Protocol required CRF’ Designing eCRF Data Validation Plan Specification Discrepancy Management SAE and External Data Reconciliation Study Build 2.Module II: CDISC-SDTM Annotation of CRF’s SDTM Mapping Specification Define.XML 3.Module III: SAS SAS programming on Data Validation SAS programming on SDTM mapping Specification SAS Programming on Define SAS Statistical Programming Diploma in Clinical Research & Clinical Data Management. Courses Highlights: Excellent Coaching By Industry Experts. Weekend Assignments & Study Material. Exposure to Live Clinical Trial Projects. Placement Assistance, Mock Interviews & Professional Development. ADDRESS: INSTITUTE OF GOOD CLINICAL PRACTICE, # 2ND FLOOR,ABOVE MORE SUPER MARKET, NEAR SRIPURAM COLONY BUS STOP, MOOSARAMBAGH, MALAKPET, HYDERABAD.

INSTITUTE OF GOOD CILNICAL PRACTICE (IGCP) GIVE Practical Exposure to Clinical research and Clinical Data Management industry..We are committed to attracting, developing, rewarding and retaining the best people in Clinical Research and Clinical Data management field to Teach conduct and support our innovative and highest quality Knowledge.IGCP-ians Success stories summaries our Reputation, our Promise and our Future as renowned organization for both Clinical Research Domain and Technical Knowledge. • Students placed in MNC’s Worldwide. • Practical training as per the industry requirement. • Training by Subject Matter Experts.(SME) • Only Institute in India to train on CDISC-SDTM. • SAS Projects On Table Listings Figures (TLF’S), SDTM and Data Validation. • Training Clinical Data management on Electronic Data Capture Tool (EDC). • 3-4Years Knowledge is guaranteed by the end of the course. • Internship Programs on Clinical Data Management & SAS Projects. Teaching Mode: Class Room and Online*

INSTITUTE OF GOOD CILNICAL PRACTICE (IGCP) GIVE Practical Exposure to Clinical research and Clinical Data Management industry..We are committed to attracting, developing, rewarding and retaining the best people in Clinical Research and Clinical Data management field to Teach conduct and support our innovative and highest quality Knowledge.IGCP-ians Success stories summaries our Reputation, our Promise and our Future as renowned organization for both Clinical Research Domain and Technical Knowledge. • Students placed in MNC’s Worldwide. • Practical training as per the industry requirement. • Training by Subject Matter Experts.(SME) • Only Institute in India to train on CDISC-SDTM. • SAS Projects On Table Listings Figures (TLF’S), SDTM and Data Validation. • Training Clinical Data management on Electronic Data Capture Tool (EDC). • 3-4Years Knowledge is guaranteed by the end of the course. • Internship Programs on Clinical Data Management & SAS Projects. Teaching Mode: Class Room and Online* FOR CLASSROOM TIMINGS: AM TO PM FOR ONLINE TIMINGS: PM TO PM ADDRESS: INSTITUTE OF GOOD CLINICAL PRACTICE, # 2ND FLOOR,ABOVE MORE SUPER MARKET, NEAR SRIPURAM COLONY BUS STOP, MOOSARAMBAGH, MALAKPET, HYDERABAD. PH:,, 040 .

INSTITUTE OF GOOD CLINICAL PRACTICE (IGCP) GIVE Practical Exposure to Clinical research and Clinical Data Management industry..We are committed to attracting, developing, rewarding and retaining the best people in Clinical Research and Clinical Data management field to Teach conduct and support our innovative and highest quality Knowledge.IGCP-ians Success stories summaries our Reputation, our Promise and our Future as renowned organization for both Clinical Research Domain and Technical Knowledge. • Students placed in MNC’s Worldwide. • Practical training as per the industry requirement. • Training by Subject Matter Experts.(SME) • Only Institute in India to train on CDISC-SDTM. • SAS Projects On Table Listings Figures (TLF’S), SDTM and Data Validation. • Training Clinical Data management on Electronic Data Capture Tool (EDC). • 3-4Years Knowledge is guaranteed by the end of the course. • Internship Programs on Clinical Data Management & SAS Projects. Teaching Mode: Class Room and Online* ADDRESS: INSTITUTE OF GOOD CLINICAL PRACTICE, # 2ND FLOOR,ABOVE MORE SUPER MARKET, NEAR SRIPURAM COLONY BUS STOP, MOOSARAMBAGH, MALAKPET, HYDERABAD. PH:,, 040 .

INSTITUTE OF GOOD CILNICAL PRACTICE (IGCP) GIVE Practical Exposure to Clinical research and Clinical Data Management industry. We are committed to attracting, developing, rewarding and retaining the best people in Clinical Research and Clinical Data management field to Teach conduct and support our innovative and highest quality Knowledge.IGCP-ians Success stories summaries our Reputation,our Promise and our Future as renowned organization for both Clinical Research Domain and Technical Knowledge. • Students placed in MNC’s Worldwide. Practical training as per the industry requirement. • Training by Subject Matter Experts.(SME) • Only Institute in India to train on CDISC-SDTM. • SAS Projects On Table Listings Figures (TLF’S), SDTM and Data Validation. • Training Clinical Data management on Electronic Data Capture Tool (EDC). • 3-4Years Knowledge is guaranteed by the end of the course. • Internship Programs on Clinical Data Management & SAS Projects. Teaching Mode: Class Room and Online* MAIL ID: WEBSITE:www.igcp.co.in FOR CLASSROOM TIMINGS: AM TO PM FOR ONLINE TIMINGS: PM TO PM ADDRESS: INSTITUTE OF GOOD CLINICAL PRACTICE, # 2ND FLOOR,ABOVE MORE SUPER MARKET, NEAR SRIPURAM COLONY BUS STOP, MOOSARAMBAGH, MALAKPET, HYDERABAD. PH:,, 040 .

OUR OBJECTIVE: TO IMPART PRACTICAL TRAINING ON CLINICAL RESEARCH / DATA MANAGEMENT AS PER ICH GCP GUIDELINES, LOCAL REGULATORY GUIDELINES AND ETHICAL GUIDELINES AND PROVIDE ‘INDUSTRY READY RESOURCES’ TO THE CLINICAL RESEARCH INDUSTRY AND THEREBY CONTRIBUTE TOWARDS DEVELOPING INDIA AS THE MOST FAVOURABLE DESITINATION FOR CLINICAL RESEARCH / DATA MANGEMENT OUTSOURCING FOR ALL PHARMACEUTICAL AND CRO INDUSTRY ACROSS THE WORLD. ABOUT US: We understand the exact requirement of the Clinical Research Industry for their need of the trained manpower as we have experience working with Clinical Research Industry since 10 years handling Clinical Trials, Clinical Data Management, SAS, Pharmacovigilance, Drug Regulatory Affairs etc. With the experience working with CRO’s, we have designed each training module focusing to expose the students practically to each task with logical exercises covering all the areas of Clinical Trials and Clinical Data Management, CDISC-SDTM and SAS. Highly experienced staffs (SME’s) from clinical research and data management industry will only will involved in training the candidates for 90 days with hands on experience on various areas of Clinical Data Management, SAS, CDISC-SDTM/ADAM. Institute of Good Clinical Practice (iGCP) provide training in two different modes like Class Room, Online-learning. UTE OF GOOD ADDRESS: INSTITUTE OF GOOD CLINICAL PRACTICE # 2ND FLOOR, ABOVE MORE SUPER MARKET, NEAR SRIPURAM COLONY BUS STOP, MOOSARAMBAGH, MALAKPET, HYDERABAD. PH:

nstitute of Good Clinical Practice (iGCP) offers different unique programs for aspiring professionals willing to pursue a career in Clinical Research, Clinical Data Management,CDISC-SDTM, and SAS. The training program aims to provide a career path for professionals from Life Sciences and Statistics background. Highly experienced staffs from clinical research and data management industry trains students with hands on experience on various areas in clinical research, Clinical Data Management, CDISC-SDTM, SAS, Pharmacovigilance,Drug regulatory affairs, Table Listings Figures (TLF’S)etc. Institute of Good Clinical Practice (iGCP) provide training in three different modes like Class Room, Online-learning for all Medical, Pharmacy and Science students and professionals aspiring to make a career in Clinical Research.

Institute of Good Clinical Practice (iGCP) offers different unique programs for aspiring professionals willing to pursue a career in Clinical Research, Clinical Data Management,CDISC-SDTM, and SAS. The training program aims to provide a career path for professionals from Life Sciences and Statistics background. Highly experienced staffs from clinical research and data management industry trains students with hands on experience on various areas in clinical research, Clinical Data Management, CDISC-SDTM, SAS, Pharmacovigilance,Drug regulatory affairs, Table Listings Figures (TLF’S)etc. Institute of Good Clinical Practice (iGCP) provide training in three different modes like Class Room, Online-learning for all Medical, Pharmacy and Science students and professionals aspiring to make a career in Clinical Research.

Institute of Good Clinical Practice (iGCP) offers different unique programs for aspiring professionals willing to pursue a career in Clinical Research, Clinical Data Management,CDISC-SDTM, and SAS. The training program aims to provide a career path for professionals from Life Sciences and Statistics background. Highly experienced staffs from clinical research and data management industry trains students with hands on experience on various areas in clinical research, Clinical Data Management, CDISC-SDTM, SAS, Pharmacovigilance,Drug regulatory affairs, Table Listings Figures (TLF’S)etc. Institute of Good Clinical Practice (iGCP) provide training in three different modes like Class Room, Online-learning for all Medical, Pharmacy and Science students and professionals aspiring to make a career in Clinical Research. Technical learning's: Extensive knowledge of drug safety and drug development process and procedures In-depth knowledge of coding principles, submission criteria, regulatory timeline requirements, technical requirements and guidelines Extensive knowledge of US and ICH safety reporting regulations and guidelines. Good understanding of IND safety reports, 21 CFR part 11 and HIPPA guidelines. Performed triage, evaluation and processing of adverse event reports from post marketing and clinical sources in accordance with FDA and ICH guidelines Working knowledge pertaining to MedDRA and WHO Drug dictionaries. Proficient in data entry and excellent knowledge of ARGUS safety database. Eligibility: Bachelor's, Master’s, or PhD, MBBS/ MD/B.D.S /M.D.S/ B.A.M.S / B.H.M.S /B.P.T/ B.Tech (Biotechnology / Pharmaceutical Science) / B. Pharm /M.Pharm /BVSC / B.Sc. (Nursing) / B.Sc./M.Sc, M.Pharmacy, M.Sc /MA (Statistics) and all professionals working with Pharmaceutical companies, CROs and Hospital.

Institute of Good Clinical Practice (iGCP) offers different unique programs for aspiring professionals willing to pursue a career in Clinical Research, Clinical Data Management,CDISC-SDTM, and SAS. The training program aims to provide a career path for professionals from Life Sciences and Statistics background. Highly experienced staffs from clinical research and data management industry trains students with hands on experience on various areas in clinical research, Clinical Data Management, CDISC-SDTM, SAS, Pharmacovigilance,Drug regulatory affairs, Table Listings Figures (TLF’S)etc. Institute of Good Clinical Practice (iGCP) provide training in three different modes like Class Room, Online-learning for all Medical, Pharmacy and Science students and professionals aspiring to make a career in Clinical Research. Technical learning's: Extensive knowledge of drug safety and drug development process and procedures In-depth knowledge of coding principles, submission criteria, regulatory timeline requirements, technical requirements and guidelines Extensive knowledge of US and ICH safety reporting regulations and guidelines. Good understanding of IND safety reports, 21 CFR part 11 and HIPPA guidelines. Performed triage, evaluation and processing of adverse event reports from post marketing and clinical sources in accordance with FDA and ICH guidelines Working knowledge pertaining to MedDRA and WHO Drug dictionaries. Proficient in data entry and excellent knowledge of ARGUS safety database. Eligibility: Bachelor's, Master’s, or PhD, MBBS/ MD/B.D.S /M.D.S/ B.A.M.S / B.H.M.S /B.P.T/ B.Tech (Biotechnology / Pharmaceutical Science) / B. Pharm /M.Pharm /BVSC / B.Sc. (Nursing) / B.Sc./M.Sc, M.Pharmacy, M.Sc /MA (Statistics) and all professionals working with Pharmaceutical companies, CROs and Hospital. ADDRESS: INSTITUTE OF GOOD CLINICAL PRACTICE, # 2ND FLOOR,ABOVE MORE SUPER MARKET, NEAR SRIPURAM COLONY BUS STOP, MOOSARAMBAGH, MALAKPET, HYDERABAD. PH:,, 040 .

Institute of Good Clinical Practice (iGCP) offers different unique programs for aspiring professionals willing to pursue a career in Clinical Research, Clinical Data Management,CDISC-SDTM, and SAS. The training program aims to provide a career path for professionals from Life Sciences and Statistics background. Highly experienced staffs from clinical research and data management industry trains students with hands on experience on various areas in clinical research, Clinical Data Management, CDISC-SDTM, SAS, Pharmacovigilance,Drug regulatory affairs, Table Listings Figures (TLF’S)etc. Institute of Good Clinical Practice (iGCP) provide training in three different modes like Class Room, Online-learning for all Medical, Pharmacy and Science students and professionals aspiring to make a career in Clinical Research. Technical learning's: Extensive knowledge of drug safety and drug development process and procedures In-depth knowledge of coding principles, submission criteria, regulatory timeline requirements, technical requirements and guidelines Extensive knowledge of US and ICH safety reporting regulations and guidelines. Good understanding of IND safety reports, 21 CFR part 11 and HIPPA guidelines. Performed triage, evaluation and processing of adverse event reports from post marketing and clinical sources in accordance with FDA and ICH guidelines Working knowledge pertaining to MedDRA and WHO Drug dictionaries. Proficient in data entry and excellent knowledge of ARGUS safety database. Eligibility: Bachelor's, Master’s, or PhD, MBBS/ MD/B.D.S /M.D.S/ B.A.M.S / B.H.M.S /B.P.T/ B.Tech (Biotechnology / Pharmaceutical Science) / B. Pharm /M.Pharm /BVSC / B.Sc. (Nursing) / B.Sc./M.Sc, M.Pharmacy, M.Sc /MA (Statistics) and all professionals working with Pharmaceutical companies, CROs and Hospital. FOR ONLINE TIMINGS: PM TO PM FOR CLASS ROOM TIMINGS: AM TO PM ADDRESS: INSTITUTE OF GOOD CLINICAL PRACTICE, # 2ND FLOOR,ABOVE MORE SUPER MARKET, NEAR SRIPURAM COLONY BUS STOP, MOOSARAMBAGH, MALAKPET, HYDERABAD. PH:,, 040 .

100% Job Oriented Medical Billing Coding/Medical Internship Training With Placements:- Organization at a Glance: Global Institute Of Advanced Pharmaceutical & Health Sciences (GIPHS) is a leading resource consulting services organization for the Pharmaceutical, Biotechnology and Medical Device industries. We Provide contract and permanent job opportunities within the Pharmaceutical, Biotechnology and Medical Device industries to experienced professionals as well as entry level candidates. The services offered fall into the broad categories of Recruitment Solutions, Temporary Staffing, Outsourcing, Consulting, Application Hands on Software Training in Clinical Data Management (Oracle Clinical, Oracle Inform/Central Designer), Pharmacovigilance (Oracle Argus Safety Database, Oracle AERS), CDISC SDTM, Medical Coding, Clinical Coding (MeDRA & WhoDrug Dictionaries) & SAS to aspirants of Clinical Research Industry. We successfully help the top Pharmaceutical, Biotechnology and Medical Device organizations from around the world to recruit high caliber experienced & trained professionals. Global Institute Of Advanced Pharmaceutical & Health Sciences (GIPHS) also provides Site Management Services, Clinical Data Management, Pharmacovigilance, Medical Writing, Medical Coding, Medical Billing, Biostatistical Analysis, SAS Programming & IT Support Services to Pharmaceutical, Biotechnology and Medical Device Organizations globally. Mode of Training- Classroom/Online Alternative day exams with focus on CPC and CCS Certification preparation. • Daily exams. • Physician and Hospital coding. GlPHS(Global Institute Of Advanced Pharmaceutical & Health Sciences)Labs Advantages: • Own Medical Coding live projects • Highest Placement record across all training institutes • Industry SOPs based training • Trainers with minimum 5 years experience The focus of the lectures will be mainly on the following topics: ICD Coding (Diagnosis Coding) CPT Coding (Procedures Coding) HCPCS Coding (Supplies Coding/Drugs Coding), Hospital Coding CPC and CCS Preparation HIPAA ComplianceICD Coding (Diagnosis Coding) CPT Coding (Procedures Coding) HCPCS Coding (Supplies Coding/Drugs Coding) Hospital Coding • CPC and CCS Preparation • HIPAA Compliance Clinical Coding • MedDRA • Structure and Content • Comparison to COSTART • Coding and the Points to Consider Document • Standardized MedDRA Queries (SMQs) • Versioning • CTCAE Mapping to MedDRA • Regulatory Expectations • Overview of the MedDRA dictionary (structure and format) • General coding principals based on the current MedDRA Points to Consider • Practical exercises in MedDRA coding • General analysis and reporting principals based on the current MedDRA Data Retrieval and Presentation: Points to Consider • Practical exercises in MedDRA analysis and reporting • Review of MedDRA • Rules and Conventions Used In MedDRA • MedDRA Term Selection: Points to Consider Document • Discussion of the Coding Examples Provided in the “Points to Consider” Document • Additional Coding Examples to Further Explain the Term Selection Points • Importance of Company Coding Conventions • WHO Drug • Review of WHO Drug • Identifying the Drug • Using a "Fuzzy" Search Engine • Search Using Google • Martindale Online • Other Web Resources • General Principles for Selecting the Appropriate WHO Drug Entry • Abbreviations • Handling Drugs with Multiple WHO Drug Entries • Special Rules for Coding Certain Drugs and Drug Categories • Multi-Ingredient Drugs • Querying Terms • Importance of Company Coding Conventions • Change Request Process • Coding Herbal Medicines • Coding Investigational Products • Coding Vaccines • Coding Multivitamins • Handling Reported Non-Therapies • Application and Use of ATC Codes • Practical Exercises in WHO Drug Coding • The Following Chapters are discussed in detail • Integumentary System coding • Musculoskeletal System coding • Respiratory System coding • Cardiovascular System coding • Digestive System coding • GenitoUrinary System coding • Neurology coding • Sense Organs coding • Radiology coding • Pathology coding • Medicine coding and Medical Billing in detail • HIPAA compliance • This course will provide training in the core competencies in Medical Coding including fundamentals of clinical trials. It's a great program for industry professionals who are looking to advance their careers or seeking industry certifications and anyone looking to enter the clinical research & Health Care Industry. We are certified members of American Academy of Professional Coders. GIPHS (Global Institute Of Advanced Pharmaceutical & Health Sciences Comprehensive Medical Coding training program provides you with the training and practical experience you need to develop the skills necessary to work as a medical coding and billing professional. Prepares you to perfection to pass national medical coding certification exams Covers the complete syllabus and meets requirements for both the AHIMA and AAPC certification exams, including the CCA, CPC, and CPC-H. As a certified coder, you will be in high demand in the job market. Instructors with Onsite/Real time experience and Certified in the field. Instructors have "been there, done that" and know not only what it takes to create career opportunities in your field of interest but also how you'll be able to apply your industry-current education once you make your move. Career-focused training programs with concentrations to help you build relevant credentials Live Project Training with Internship will also be provided in Health Care BPOs. Mode of training- Instructor Led Class room/ Online Training Tenure: 2 month Eligibility Applicants are recommended to have Any life Science degrees: Bachelor's(B.Sc Life Sciences), Master’s (M.Sc Life Sciences), or PhD, MBBS/ MD/B.D.S /M.D.S/ B.A.M.S / B.H.M.S /B.P.T/ B.Tech (companies, CROs and Hospitals. Certification: Biotechnology / Pharmaceutical Science) / B. Pharm /M.Pharm /BVSC / B.Sc. (Nursing) / B.Sc./M.Sc, M.Pharmacy, M.Sc /MA (Statistics) and all professionals working with Pharmaceutical Certificate will be provided for this course on successful completion of Assignments & Projects. Certificate would be awarded at the end of the program by Global Institute Of Advanced Pharmaceutical & Health Sciences For more information, please contact Global Institute of Advanced Pharmaceutical & Health Sciences at Training Location (Venue) GIPHS (Global Institute of Advanced Pharmaceutical & Health Sciences) Academy of Clinical Research KVR Enclave, #nd Floor,Beside Satyam Theater,Near Maitrivanam, Ameerpet, Hyderabad. Contact Information Dr.Anita Singh Training Coordinator Mob No:+91