Regulatory

COVALENT:- Covalent is a group of company which has services and operations in Clinical, Information Technology, Energy, consumer products, Power and Infrastructure. Training @ Covalent:- We arededicated to establish ourselves as ''A values-driven organization''. These values will continue to direct our growth and organization’s operation. “Covalent” values supporting the way like “Kreative”. Regulatory Affairs(RA) Training or Course:- Introduction to different types of Pharmaceutical products: Basic concepts on Rx, OTC, API, Starting material, DP/FP, Generics vs. Innovator drugs, Biologics vs. Biosimilars, Laws vs. Regulations vs. guidelines. Drug discovery and development Worldwide regulatory agencies and their role Approval process for each of the below products in US/EU/India: [covers development path, submissions, regulatory expectation for development, approval and market] Post-market regulatory obligations GLP’s: 21 CFR 58 -The History of GLP, The Idea behind GLP, The Areas of Application, The Pillars of Good Laboratory Practice, Where Can GLP be Profitably Applied?, Indian GLP and International GLP. CMC topics: GMP (US/EU/Indian/ PIC), Preformulation studies (Drugs and Generics), ICH Q 7 guideline, 21 CFR 210 and 211, Medical device CE marking and ISO certifications. Audits, pre and post approval Inspections, handling post inspection/ audit queries. Collecting, organizing and compiling various regulatory submissions in compliance with the applicable regulations: ASEAN and BRIC regulations and registration process of Drugs and Biologics. Different stages of interactions, briefing packages, responses and corrective measures during drug approval process with FDA. PDUFA meetings and advisory committee meetings with US FDA, EU scientific advisory committee. Regulations of Drugs and cosmetics Act, and its importance to Indian pharma industry. Recent regulatory changes in Indian DCGI and compiling dossiers for various DCGI submission: Hands on workshops in next 15 days: Word template of CTD structure. Hands on work of filling different regulatory forms in US/EU/India. Preparing for Regulatory interviews (Example interview questions will be provided). Communication skills. 2-3 seminars each of individual students to enhance their confidence and presentation skills. Explaining the real difficulties faced in a pharma industry and providing Corrective and Preventive Actions (CAPA). Training Duration (Classroom/Online): 3-Months/2-Months Training Fee: 20K/25k + Taxes Mobile: Website:- http://covalentech.com/regulatory_affairs.html

Groupware Training is offering Regulatory Affairs training in Hyderabad with real time faculties. To know more Contact: Mobile: +91-

COVALENT:- Covalent is a group of company which has services and operations in Clinical, Information Technology, Energy, consumer products, Power and Infrastructure. Training @ Covalent:- We arededicated to establish ourselves as ''A values-driven organization''. These values will continue to direct our growth and organization’s operation. “Covalent” values supporting the way like “Kreative”. Training Duration (Classroom/Online): 3-Months/2-Months Training Fee: 20K/25k + Taxes Mobile: Website:- http://covalentech.com/regulatory_affairs.html

Type Distance learning courses PG Diploma in Drug Regulatory Affairs from NIMS University Distance Education The pharmaceutical, biotechnology and medical device research and development industries are among the most highly regulated industries globally. As pharmaceutical sector is growing rapidly, there is a need of regulatory affairs professionals to cater the current needs of industries for the global competition. Regulatory affairs professionals are the link between pharmaceutical industries and worldwide regulatory agencies. Pharmaceutical Industry, being one of the highly regulated industries, is in immense need of people than ever before who are capable of handling issues related to regulatory affairs in a comprehensive manner. Program Code best PGDDRA PGDDRA Duration Min. Duration 1 Years Max. Duration 3 Years Eligibility Criteria Graduate in Science Stream Tution Fees per annum / After the completion of PGDDRA, you will find a challenging career in a hospital and healthcare industry Common job profiles of students after completing PGDDRA include: Medical and Health Services Managers, Hospital Administrator, Manager, Senior Manager, Hospitals and other Senior Leadership Positions.

Covalent is one of the leading training institutes for Regulatory Affairs in Hyderabad.Course Content of RA is Introduction to different types of Pharmaceutical products: Basic concepts on Rx, OTC, API, Starting material, DP/FP,Biologics vs. Biosimilars, Laws vs. Regulations vs. guidelines. Worldwide regulatory agencies and their role Approval process. Post-market regulatory obligations GLP’s: 21 CFR 58 -The History of GLP, The Idea behind GLP, The Areas of Application, The Pillars of Good Laboratory Practice,,Indian GLP and International GLP. CMC topics: GMP, Preformulation studies, ICH Q 7 guideline, 21 CFR 210 and 211, Medical device CE marking and ISO certifications.

RAAJ GLOBAL PHARMA REGULATORY AFFAIRS CONSULTANTS [RAAJ GPRAC], Thane-Mumbai is an ISO certified 29990-2010, and NSDC accredited institute for Pharma training and Upskilling.JOBS available with training into Global Regulatory Affairs, QA-QM, Clinical, PV, CTD/eCTD/ACTD/NeeS Regulatory submissions etc. 100% JOB Guarantee. Eligibility- B.Pharm, M.Pharm, B.Sc, M,Sc, B.Tech, M. Tech and Life sciences graduates and Pharma working professionals.

Warm greetings from 'Institute of Pharmaceutical Management'! IPM is a well established organization working for “Escalating efficiency of pharma aspirants”. Over a span of 8 years, IPM has a myriad of achievements like receiving numerous national and international enrollments, conducting RA course at Astrazeneca Bangalore and has 4 branches in India as of now. IPM is organizing a one day seminar on “Drug Master File of API- Understanding and meeting current regulatory requirements “at Sipra labs, Sanathnagar, Hyderabad on 25 April . The speaker is Ms. Anagha Maharao - whose erudition will certainly enrich the knowledge of attendees. Explanation will be based on live example of API. We are pleased to invite participants from your organization to attend the seminar. Solicit prompt and prolific registrations from your esteemed organization. Please send a mail for brochure and registration form

IACS Managers each have an in-depth understanding of individual overseas markets and the dynamics of specific trades. This expertise enables them to provide you with market-specific, local advice on factors affecting the transit of your cargo. This might include: Terminal conditions. Local or overseas transport infrastructure. Berthing delays or congestion. Local or overseas regulatory and political changes. Any relevant customs procedures. So whether you re importing or exporting, working with IACS will plug you into a network of experts across more than 493 offices, planning 200 global routes to 500 ports in over 155 countries, and we re committed to offering competitive rates and transit times.

This is a self-study guide for the {ECA Certified Regulatory Affairs Manager} Video Course. It covers all the information that candidates need to know in order to pass this certification examination.

Sahitya bhawan publication book for all commerce background student

Greetings from ‘Institute of Pharmaceutical Management’ IPM- Mumbai based pharma training institute & consultancy firm Ms. Anagha Maharao – Managing Director Principal trainer and favourite tutor among IPM students with 28 years of experience in Pharma industry. Lectures are delivered by Anagha Maharao with the team of leading Pharma industry experts. Services offered Training: Classroom, Distance learning, Onsite training at company premises GMP compliance Regulatory consultancy Training programmes: Classroom [Sunday batches] Distance Learning Drug Regulatory AffairsDrug Regulatory Affairs Analytical Data ReviewQuality Assurance International Business DevelopmentQuality Control Upcoming batches []: Classroom [Sunday batches]Tenure [Months]CommencementVenue International Business development2 1 March Thane Drug Regulatory affairs 631May Dombivli International Business development2 7 June Borivali Analytical Data Review 2 14 June Thane Drug Regulatory affairs 2 21 June Borivali Drug Regulatory affairs 2 26 July Vashi Features: Contents based on current approach of regulatory agencies Case study based teaching pattern User friendly notes Group discussions Evaluation by exam Placement assistance Achievements 8th year of excellence Running courses at various locations in Mumbai & Navi-Mumbai National and international enrollments International enrollments- Spain, New York, UK, South Africa, Vietnam, Oman, Dubai, Johannesburg & Bangladesh Recently, IPM conducted RA program at Astrazeneca, Bangalore [European company], IDMA Vadodara & more… For details contact: Vidyesh Maharao O: - M: / Note: If you wish to unsubscribe, please mention “Unsubscribe’ in the subject of the reply mail.

Introduction: A Course designed to completely engage you in Computer system Validation for the present Needs. This Course delivers Hands on experience knowledge on how CSV is treated and looked at in the present times. You will be ready for how to select the right validations and right controls (Technical and Procedural) Know how on handling PLC's. Challenges: Data Integrity with Documentation Identifying right and appropriate Procedural and Technical controls How Agile methodology works for Cat 5 development Learning Objectives: Role of FDA CSV Points and why Validate GAMP Relation between 21 CFR Part 11, Annex 11 and 211 Risk Assessments Data Integrity CSV Deliverables (Technical and Procedural controls) How to have an SOP and benefits and following the SOP's Compliance Challenges: The confusion due to what are often contrary interpretations of CSV requirements, the focus on generating extensive CSV packages, and fear of not meeting regulatory expectations turn many CSV projects into major endeavors that lose sight of the contribution to quality and compliance. A harmonized and consistent risk-based CSV is an effective way to optimize the investment allocated to corporate compliance programs. Target Audience: A must attend the seminar for professionals in Pharmaceuticals, QC Laboratories, APIs, Finished Products, Contract Laboratories, CROs, Medical Device & Biotech companies, and Suppliers of Computer Systems. DEPARTMENTS: Quality Control & Quality Assurance, Research and Development, Laboratory and Regulatory Compliance, IT/IS & Software Departments, Production & Manufacturing, Documentation, Training Departments PROFESSIONALS: Managers and Supervisors, Senior Managers and Team Leaders, General Managers, Analytical Chemists, Validation Specialists, Laboratory Managers and Supervisors, Regulatory Affairs Managers, Documentation Specialists & Analysts, Consultants, and Systems Administrators

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:

Under Graduate BCA BSc (Information Technology) BSc (Infrastructure Management System) Post Graduate MCA MSc (Information Technology) Arts & Humanities and Vocational Sciences Under Graduate BA (Journalism and Mass Communication) Post Graduate MA (Journalism & Mass Communication) Health Care Services Under Graduate +3 More BSc (Biotechnology) BSc (Health Information Administration) BSc (Medical Imaging Technology) BSc (Medical Laboratory Technology) Post Graduate MSc (Bioinformatics) MSc (Clinical Research and Regulatory Affairs) PGD (Bioinformatics) PGD (Clinical Research and Regulatory Affairs)

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 .

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 .

About Medicity Research Institute Pvt. Ltd We are pleased to introduce The Medicity a leading learning platform with the sole purpose to provide future doctors and already practicing surgeons with the best surgical techniques and skills to enhance their surgical skills through the certification courses. Our website is a repository of reliable and authentic information for over 328+ Hospitals, 245+ courses, and more than 3500+ students who have successfully completed their training.themedicity.com is India’s smartest online platform that blends knowledge, with technology, innovation, and credibility to give students personalized insights to make informed career, course decisions. We offer specific information for students interested in courses in India (themedicity.com) across the most popular fields of Gynecology, infertility, Medicine, surgery, Orthopedic, Obstetrics, Pathology, Diabetes, Pediatrics, Ophthalmology, and many such programs. We work closely with our new medical aspirants to get a personalized experience on our site, based on educational background and career interest. Job Description Serves as a senior medical writer on clinical study or regulatory project teams. Writes, edits, and coordinates content for clinical/regulatory while serving as primary technical contact with the internal team and the client. Creating doctor/hospital profiles and blogs on our website. Creating medical packages for website visitors, and our internal teams. Conceptualizing and creating content for YouTube and social media platforms. Our primary requirement is for English. Required Candidate profile · Must have strong writing skills in English. · At least 1 year of professional writing experience. · Past experience for writing on healthcare or having a medical background is preferred. · Ability to write grammatically correct and crisp sentences · Awareness of SEO practices · Ability to research on internet and organize the information. · Self starter who can work with less guidance · Absolutely no plagiarism You can call us for more information at - 9540915409

B. Tech Aircraft Maintenance Engineering is an advanced professional Degree program designed and Developed to industry requirement as per the guideline of the Regulatory body of civil aviation Authority. This course provides an opportunity for students to learn the program through theoretical & practical learning and also in the maintenance Organization. Students also can appear for license examinations as an individual candidate. Upon clearing all the modules as required by the Regulatory Body he will become eligible to be a Qualified Aircraft Maintenance Engineer. The prime responsibilities of the Aircraft Maintenance Engineers include carrying out repairs, troubleshooting problems, conducting inspections to keep aircrafts in flying condition. No aircraft can take-off until it's signed by an Aircraft Maintenance Engineer. Prior to the take-off of the aircraft, the Aircraft Maintenance Engineers inspect the aircraft and sign the Certificate ensuring safety. Aircraft Maintenance Engineering Eligibility Criteria For Aircraft Maintenance Engineering eligibility is 12th pass with Physics, chemistry and Mathematics or diploma in engineering from recognised board or University. Candidate age at the time of admission should be minimum 16 years. Candidates must pass a general medical test & colour blindness test. Candidates passed from NIOS can also register for admission. Aircraft Maintenance Engineering Course Duration B. Tech in Aircraft Maintenance Engineering is a 4 years programme divided into 8 semesters of 6 months each. Aircraft Maintenance Engineering program includes theoretical & practical learning. Last 1 year is full practical/industrial Training.

Oracle Identity Management -8179736190 We are providing Oracle Identity Management (OIM) under Yashwanth, MTech, and Technical Manager in CMMI Level 5 Company with 9+ years of middleware experience Oracle Identity Management is a complete and integrated, next-generation identity management platform that provides breakthrough scalability; enables organizations to achieve rapid compliance with regulatory mandates; secures sensitive applications and data regardless of whether they are hosted on-premise or in a cloud; and reduces operational costs. Course Contents • Introduction • Identity Management: Overview • Understanding Oracle Identity Manager • Installing and Configuring Oracle Database • Installing and Configuring Oracle Weblogic Server • Installing and Configuring Schema for OID & OVD using RCU • Installing and Configuring Identity Management Suite • Upgrading Database Schema for Identity Management • Installing and Configuring Oracle Identity Manager • Starting and Understanding Oracle Identity Manager Consoles • Managing Users and User Entities • Using Predefined Connectors • Assigning Oracle Identity Manager Connectors to Users • Provisioning User Resources Manually • Provisioning User Resources Automatically • Expanding the Provisioning Workflow • Approving the Provisioning Workflow • Understanding Reconciliation • Performing Reconciliation • Understanding and Using Attestation Processes • Customizing the OIM Administrative and User Console

SAP Global Trade Services online training SAP Global Trade Services Overview (GTS) SAP Global Trade Services (SAP GTS) automates global trade processes and enables you to manage large numbers of business partners and high volumes of documents, while also helping you to comply with changing legal regulations. It facilitates global trade by providing you with the tools you require to respond to governments modernizing their systems and to customs authorities communicating electronically with businesses. SAP Global Trade Services (SAP GTS),can manage all the complexities of international trade including full regulatory compliance, electronic communication with customs authorities, and risk mitigation, while importing and exporting on a global basis. Business Content for SAP GTS enables you to analyze your import and export transactions and perform strategic reporting for the following areas: SAP Customs Management: "Customs Processing" service SAP Customs Management: "Transit Procedure" service SAP Risk Management: "Preference Processing" service SAP Risk Management: "Restitution" service SAP Compliance Management: "Import/Export Legal Control" service A large amount of transaction data and master data is available in SAP GTS. A selection of the data is extracted into SAP NetWeaver Business Intelligence (BI) and evaluated there. Online Training Features 1. Interactive Learning sessions 2. Industry Savvy Trainers 3. Learn Right from Your Place 4. Customized Curriculum 5. Highly Affordable Courses 6. Support after Training 7. Placement Services for H1B / EAD status holders* About Acutesoft ACUTE SOFT is a Global Interactive Learning company started by proven industry experts with an aim to provide Quality Training in the latest IT Technologies. ACUTE SOFT has a pool of Expert Trainers worldwide on all the technologies to train the students. ACUTE SOFT is offering online Training services to Major IT giants and to individual students worldwide. We also provide online training on SAP FICO,SAP SD,SAP WM,SAP PP,SAP MM,SAP SRM,SAP FSCM,SAP MDM,SAP APO, SAP IS RETAIL,SAP CRM,SAP ABAP,SAP BI,SAP BASIS,SAP BO,SAP HANA,SAP BPC,SAP ESS-MSS,SAP CS,SAP PLM,SAP GTS And SAP SNC. Experience the Quality of our Online Training. For Free Demo Please Contact Santhosh /Lakshmi: INDIA: +91-9848346149, +91-7702226149 Land line: +91 (0)40 - 42627705 US: +1 973-619-0109, +1 312-235-6527 UK :+44 207-993-2319 Skype id : acutesoft http://www.acutesoft.com http://training.acutesoft.com

Oracle Identity Management -8179736190 We are providing Oracle Identity Management (OIM) under Yashwanth, MTech, and Technical Manager in CMMI Level 5 Company with 9+ years of middleware experience Oracle Identity Management is a complete and integrated, next-generation identity management platform that provides breakthrough scalability; enables organizations to achieve rapid compliance with regulatory mandates; secures sensitive applications and data regardless of whether they are hosted on-premise or in a cloud; and reduces operational costs. Course Contents • Introduction • Identity Management: Overview • Understanding Oracle Identity Manager • Installing and Configuring Oracle Database • Installing and Configuring Oracle Weblogic Server • Installing and Configuring Schema for OID & OVD using RCU • Installing and Configuring Identity Management Suite • Upgrading Database Schema for Identity Management • Installing and Configuring Oracle Identity Manager • Starting and Understanding Oracle Identity Manager Consoles • Managing Users and User Entities • Using Predefined Connectors • Assigning Oracle Identity Manager Connectors to Users • Provisioning User Resources Manually • Provisioning User Resources Automatically • Expanding the Provisioning Workflow • Approving the Provisioning Workflow • Understanding Reconciliation • Performing Reconciliation • Understanding and Using Attestation Processes • Customizing the OIM Administrative and User Console

Type Tutoring ntroduce paramedical programmes Paramedical Programmes Diploma in Medical Lab Technology- per year Bachelor of Medical Lab Technology- per year Master of Medical Lab Technology- per year Diploma in Ophthalmic Technology- per year Bachelor of Optometry and Ophthalmic Technology- per year Master of Optometry and Ophthalmic Technology- per year Diploma in Radiography Technology- per year Bachelor of Radiation Technology- per year Master of Radiation Technology- per year - Diploma in Operation Theatre Technology- per year Diploma in ECG Technology- per year Bachelor of Occupational Therapy- per year Master of Occupational Therapy- per year PG Diploma in Geriatric Medicine- per year PG Diploma in Maternal and Child Health PG Diploma in Drug Regulatory Affair

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

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Pharmacovigilance Training & Placements The course modules cover theoretical aspects of pharmacovigilance through a structured curriculum. The course will put emphasis on interactive sessions with the participants, hands-on approach on the Argus database with case assignments, group discussions and quizzes as evaluation components Overview of Pharmacovigilance Regulatory Aspects of Pharmacovigilance Periodic Safety Updates Reports(PSUR's) Suspected Unsuspected Serious Adverse Reactions Care Reporting Process Eudra Vigilance Signal detection Process and tools Safety Intelligence Practical and Hands- on Oracle Argus Data Base Eligibility criteria for admission Applicant should have a Bachelor’s or Master’s Pharmacy & MBBS And All Medicine Students. Pharmacovigilance is a growing sector. With increased outsourcing and the advent of tightened regulations by the regulators, there will be a lot of scope for professionals who are ‘pharmacovigilance-ready’. The placement opportunities can be from CROs, BPOs or Pharmaceutical companies. Course Duaration: 2months (50) Contact: Lara Clinical Research #nd floor,Nilgiri Block,Aditya Enclave Ameerpet,Hyderabad Get Trained and Placed in Pharma, CRO, MNC Industries Do you have a Background in Science, Medicine or Related Area? Do you wish to pursue a career in Clinical Research Industry? Do you wish to become a Clinical Research professional? Do you wish to become a Clinical Data Professional? Do you wish to become a SAS Programmer or Analyst? Do you wish to become a Drug safety Associate (PV) Professional? Do you wish to become a Medical Coder professional? If your answer to any of the above question is “YES” then Contact us to get you started on diverse Training opportunities in Lara Clinical Research Training Institute. Lara Clinical assists life science and healthcare professionals achieve success by delivering specific solutions for their individual needs, our Popular Training Programmes. Course Curriculum: 1)Clinical Research & Data Management 2)Clinical Data Management & Pharmacovigilance 3)Clinical Data Management with SAS Clinical Programming 4)Pharmaco vigilance 5)Medical Coding 6)CDISC/SDTM 7)SAS-Clinical To enroll in any of these courses and packages tailored to to your needs contact at any by emailing Lara Clinical Research, Ameerpet Hyderabad Calling Pharmacy professionals, Medicine professionals, Life science Studnets, IT Students Training will be conducted in Hyderabad Ph: 040-,

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) 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. ADDRESS: INSTITUTE OF GOOD CLINICAL PRACTICE, # 2ND FLOOR,ABOVE MORE SUPER MARKET, NEAR SRIPURAM COLONY BUS STOP, MOOSARAMBAGH, MALAKPET, HYDERABAD. PH:,, 040 .