Sas cdm training assurance

SAS Press can help you share your knowledge and expertise worldwide.It is manifested that businesses find it really challenging to handle the big data that continue to grow in the world of terrific competition. In order to sustain in this competition, it becomes quite crucial for the business to take their business decision with great pace so that they can match the changes in the market. Advanced and synchronized data analytics are required for the same. Here lies the effectiveness of SAS that is the acronym of Statistical Analysis System. If you wish to enjoy the challenge in your career that would bring huge success for you, it would be wise on your part to undergo the training program that is aimed to offer you the required knowledge about SAS. NAVEEN TECHNOLOGIES About training centre: NAVEEN TECHNOLOGIES I is the best online training to provide the SAS,SAS BI,SAS CLINICAL RESEARCH,SAS CDM AND SAS CERTIFICATION EXAM online trainings and out marketing employs available 24/7.NAVEEN TECHNOLOGIES is the Best Online Training Center for SAS in Hyderabad, in India. The Trainer having around 8 years of experience. And they provide Real-time practical Oriented Training. The SAS material prepared bygoodonlinetrainings.com by expert trainers. We are providing the best online training and corporate training through National and International. call us at India: + USA: +

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High Profiled having 12+yrs of Real Time Experience on SAS Online Training by Industry Experts sas Technology is the biggest knowledge gateway and the best way to predict the future for the people in the SQL Database Administration World - "SAS Training for you, would be a definite advantage to jump start your IT career immediately and effectively" SAS ONLINE TRAINING Goodonlinetrainings is a Global Interactive Learning company started by proven industry experts with an aim to provide Quality Training in the latest IT Technologies. Goodonlinetrainings has a pool of Expert Trainers worldwide on all the technologies to train the students. Goodonlinetrainings is offering Training services to Major IT giants and to individual students worldwide. Good Online Trainings Institute marketing employs available 24/7. Students can reach us by dropping emails to the register mail id and phone calls. Please drop an email with your contact details so my marketing employs will reach you as soon as possible. Good Online Trainings Reach US at GOOD Online Trainings, Kukatpally, Hyderabad. Goodtrainingonlines provides the best specialized Computer Training & Software training for various Computer IT courses. Good Online Training which is a high profiled SAS online training institute in Indi a offers online training with real time experts and with real time concepts. We are provide online training & corporate training, handly online training following technologies sas , sas bi(bussines analyst ) sas cdm Contact Details : K.Naveen SAS Trainer +91-9177856619 (INDIA) 001-214-347-4655 (USA) Knaveen.sas@gmail.com goodonlinetrainings@gmail.com For further details: www.goodonlinetrainings.com/sas-online-training

High Profiled having 12+yrs of Real Time Experience on SAS Online Training by Industry Experts sas Technology is the biggest knowledge gateway and the best way to predict the future for the people in the SQL Database Administration World - "SAS Training for you, would be a definite advantage to jump start your IT career immediately and effectively" SAS ONLINE TRAINING Goodonlinetrainings is a Global Interactive Learning company started by proven industry experts with an aim to provide Quality Training in the latest IT Technologies. Goodonlinetrainings has a pool of Expert Trainers worldwide on all the technologies to train the students. Goodonlinetrainings is offering Training services to Major IT giants and to individual students worldwide. Good Online Trainings Institute marketing employs available 24/7. Students can reach us by dropping emails to the register mail id and phone calls. Please drop an email with your contact details so my marketing employs will reach you as soon as possible. Good Online Trainings Reach US at GOOD Online Trainings, Kukatpally, Hyderabad. Goodtrainingonlines provides the best specialized Computer Training & Software training for various Computer IT courses. Good Online Training which is a high profiled SAS online training institute in Indi a offers online training with real time experts and with real time concepts. We are provide online training & corporate training, handly online training following technologies sas, sas bi(bussines analyst) sas cdm Contact Details: K.Naveen SAS Trainer +91- (INDIA) (USA)

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.

SAS Clinical research organization oriented training in elegant it services in marathahalli. 1. History of SAS 2. SAS comes in ERP sector or not? Why? 3. Role of Statistical Analysis in Clinical Research Study and Banking analysis 4. SAS role in Clinical Research Study and Banking analysis 5. Data modeling and Data mining concepts 6. Project management in Clinical Research Study analysis and Banking analysis 7. What is Clinical research Study? 8. What is Protocol and role of Protocol in Clinical Research Study? 9. What is randomization and non randomization? Which is playing 10. Main role in Clinical research study? 11.What is SOP (Standard operating Procedure)? 11. What is DBMS? 12. Role of DBMS team in Clinical Research Study 13. What is CDM (Clinical data management)? 14. Importance of CDM systems for data loading 15. What is SAP (Statistical Analysis Plan)? 16. Role of SAP in Clinical Research Study 17. SAS Work Flow in Clinical Research Study 18. Relation between SAS and DBMS 19. Interaction between SAS with CDMs for data access 20. Various report generation in Clinical Research Study 21. Role of SAS in Credit Analysis and Different Banking Channels 22. When will go any Industry for Data modeling and Data mining 23. Role of SAS in Data modeling and Data mining GETTING STARTED WITH SAS SYSTEMS: 1. Basic operating system commands, operating system file structures 2. Managing windows in SAS window environment 3. How to run SAS application in different modes and in different environment like Windows, Unix and Mainframes. 4. Use of different kind of SAS products and how to use in SAS application. 5. Difference between the SAS products. 6. Why using the SAS in different sectors 7. How to use the Data Step to read and manipulate complex forms of data 8. Write Data and Proc Steps 9. Data step compile and execution 10. To run SAS application on different modes 11. Reading internal raw data into SAS 12. Read any type of external raw data into SAS 13. Reading raw data SAS environment into DATASET using Input statement & advance INFILE Statement options 14. Working with Data Storage in SAS libraries creation for user defined libraries and multi-engine architecture 15. Using a single libref to reference some or all SAS libraries reading and printing mixed records formats 16. Reading packed and zoned decimal data Working with EBCDIC and ASCII data 17. Reading data from dataset to another dataset 18. To manage the SAS window environment use with Global options 19. Reducing memory requirements with BUFFNO and BUFSIZE working with SAS dataset options 20. To manage existing data with controlling statements and expressions 21. Creating summary information, SAS functions, transforming data 22. Changing variable types using the PUT and INPUT functions Summarizing Data Files 23. Generation Data Sets to create historical information SAS 24. To export data from datasets to delimiter files using with dataset block 25. Understand error messages in the SAS log and debug your program 26. Use with error handling concepts Thanks&Regards Elegant IT Services, #nd Floor, Aswath Nagar,Varthur main road, Opp Safal Fresh,Near Railway Fly Over Maratha halli,Bangalore

SAS Clinical Research Trainers required for elegant it services good salary based on training quality 1. History of SAS 2. SAS comes in ERP sector or not? Why? 3. Role of Statistical Analysis in Clinical Research Study and Banking analysis 4. SAS role in Clinical Research Study and Banking analysis 5. Data modeling and Data mining concepts 6. Project management in Clinical Research Study analysis and Banking analysis 7. What is Clinical research Study? 8. What is Protocol and role of Protocol in Clinical Research Study? 9. What is randomization and non randomization? Which is playing 10. Main role in Clinical research study? 11.What is SOP (Standard operating Procedure)? 11. What is DBMS? 12. Role of DBMS team in Clinical Research Study 13. What is CDM (Clinical data management)? 14. Importance of CDM systems for data loading 15. What is SAP (Statistical Analysis Plan)? 16. Role of SAP in Clinical Research Study 17. SAS Work Flow in Clinical Research Study 18. Relation between SAS and DBMS 19. Interaction between SAS with CDMs for data access 20. Various report generation in Clinical Research Study 21. Role of SAS in Credit Analysis and Different Banking Channels 22. When will go any Industry for Data modeling and Data mining 23. Role of SAS in Data modeling and Data mining GETTING STARTED WITH SAS SYSTEMS: 1. Basic operating system commands, operating system file structures 2. Managing windows in SAS window environment 3. How to run SAS application in different modes and in different environment like Windows, Unix and Mainframes. 4. Use of different kind of SAS products and how to use in SAS application. 5. Difference between the SAS products. 6. Why using the SAS in different sectors 7. How to use the Data Step to read and manipulate complex forms of data 8. Write Data and Proc Steps 9. Data step compile and execution 10. To run SAS application on different modes 11. Reading internal raw data into SAS 12. Read any type of external raw data into SAS 13. Reading raw data SAS environment into DATASET using Input statement & advance INFILE Statement options 14. Working with Data Storage in SAS libraries creation for user defined libraries and multi-engine architecture 15. Using a single libref to reference some or all SAS libraries reading and printing mixed records formats 16. Reading packed and zoned decimal data Working with EBCDIC and ASCII data 17. Reading data from dataset to another dataset 18. To manage the SAS window environment use with Global options 19. Reducing memory requirements with BUFFNO and BUFSIZE working with SAS dataset options 20. To manage existing data with controlling statements and expressions 21. Creating summary information, SAS functions, transforming data 22. Changing variable types using the PUT and INPUT functions Summarizing Data Files 23. Generation Data Sets to create historical information SAS 24. To export data from datasets to delimiter files using with dataset block 25. Understand error messages in the SAS log and debug your program 26. Use with error handling concepts Thanks&Regards Elegant IT Services, #nd Floor,Aswath Nagar Varthur main road,Near Railway Fly Over Maratha halli,Land mark: Chemmunar Jewellers,

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 .

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. 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 .

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 .

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 .

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: