IGMPI is conferred with ASSOCHAM Services Excellence Award 2017: Our Directors Mr Syed S. Abbas & Mrs Rafat Abedi, Chief Advisor Dr Mahesh Gupta, Advisor Mr Amitabh Srivastava are being honoured by the Chief Guest & Honorable Member of Parliament Dr. Udit Raj

 Recipient of QCI - D.L. Shah National Quality Award

Recipient of QCI - D.L. Shah National Quality Award

Targeting to fill up the gap between the existing and accessible knowledge

Targeting to fill up the gap between the existing and accessible knowledge

 

Executive Diploma in Pharmacovigilance

Executive Diploma in Pharmacovigilance [Six months programmes approved by Quality Council of India (QCI), Govt of India]

Pharmacovigilance is an inseparable part of ever growing and recession proof CR industry. Only professionally trained employees get to make their mark and reach pinnacles of success in this fast moving sector of the health care industry. Thus IGMPI targets to teach, train and polish aspirants as Clinical Research professionals with clear understanding and complete knowledge of the industry and its working.

The Executive Diploma in Pharmacovigilance aims to benefit the professionals working in the various CR industries as it is structured by experts from the industry themselves and so global coverage and understanding of the industry and its functional areas is promised.

Module 1: Introduction to Pharmacology, Clinical Trials and Pharmacovigilance

Module 2:  Adverse Drug Reactions and Safety Reports

Module 3: Methodologies in Pharmacovigilance

Module 4: Management Systems of Pharmacovigilance and its Importance

Module 5: Seriousness & Expectedness & Causality Assessment

Module 6: Aggregate Safety Reports

Module 7: Pharmacovigilance Regulations in Various Countries

Module 8: Pharmacovigilance Programme in India (PVPI)

Module 9: Signal Detection and Data Mining

Module 10: Pharmacovigilance of Herbal Drugs & Medical Devices

Module 11: Pharmacovigilance Compliance and Inspections

Module 12: Case Study

Experimental Training

1. Introduction to Oracle AERS

2. Preparation of PSUR for submission in EU

3. MeDRA Coding

4. Eudravigilance medicinal product dictionary

5. Introduction to Argus

6. WHODD Coding

7. Signal detection and Data mining-Statistical and non-statistical

8. Introduction to Aris G Pharmacovigilance and safety

Experimental training along with the lectures from expert professionals will help the participant to learn the practical aspects of pharmacovigilance process. After the course completion, the participant is expected to have extensive and up-to-date knowledge of pharmacovigilance industry and pharmacology, PSUR for adverse reaction reporting, MeDRA and WHODD Coding, etc.

Eligibility

All those who have completed their Graduation or Post Graduation/ Pharma / PhD are eligible to enroll for the course. As this course is truly professional and industry oriented, experienced individuals worked in any sector (production, processing, quality, trial, R&D etc.) in the healthcare industry (Food manufacturing, Food Ingredient and Additive processing, Drugs manufacturing , Medical Device, Ayurvedic, Pharmaceutical Industry Regulation, Clinical Research, Homeopathic or Ayurvedic Medicine Manufacturing, Cosmetic Manufacturing, Biotechnology) can also seek benefits of the course.

Programme Duration

6 months

Registration

The registration dates for this annual program run by the institute are updated timely on the webpage.

Internship

All the efforts will be made in the form of 6 weeks internship  to provide industrial exposure to the students through internship with pharmaceutical company so that they can have good practical knowledge beyond the classroom experience.

Examination & Certification

All the participants are obliged to appear for annual exam at the end of the course. After successful completion, the participants will be awarded Executive diploma in Pharmacovigilance jointly by Quality Council of India(QCI) and Institute of Good Manufacturing Practices India (IGMPI). For all the above mentioned modules elaborate course material and project work details would be provided by the Institute from time to time. Details get updated on the webpage as well

Placement Assistance & Corporate Relations

The Institute has partnered with many organizations for providing with placement assistance to in its participants. The robust placement cell comprises of senior level Human Resources professionals and Talent Acquisition experts which maintains close links with business and industry. We are engaged in promoting the employability of our participants by maintaining good rapport and relation with HR cell and recruiting managers of leading healthcare companies across the globe.

The efforts of our placement cell also include helping with professional resume writing, interview skills & conducting mock interviews etc.

In recent months the Institute has witnessed more and more participation from professionals working with global pharmaceutical, healthcare, food giants and CROs like Dr. Reddy s Laboratories, Aurobindo Pharma, Glenmark Generics, Cipla, Wockhardt, Pfizer, Abbott, Medtronic, Foster Corporation, Ipca Laboratories, Calyx, Mother Dairy, Bliss GVS Pharma, Al Rawabi, Almarai, Green Pastures, SeQuent, PepsiCo India, Mankind, Beryl Drugs, Allergy Therapeutics, CFTRI, Ciron, Sun Pharmaceutical, Novartis, GlaxoSmithKline, Ranbaxy, Biocon, Wipro, Fortis Clinical Research, Quintiles, SRL Ranbaxy, Accenture, etc.

Future career prospects of Pharmacovigilance Training

IGMPI offers professional and industry oriented training in Pharmacovigilance thus opening doors for entry into the industry. Executive diploma in PV adds advantage for those already in the industry as a tag of professional training and those new to the industry feel comfortable with backing of apt and up-to-date information and training required to have sustained growth in the industry. Executive Diploma in Pharmacovigilance is a comprehensive course offering candidate with knowledge and practically important information about the industry type, working modalities, methodology used, techniques of quality control, drug development precisely but whole emphasis remains on Pharmacovigilance. This includes in depth study of varied types of adverse effects, serious adverse effect, adverse effect reporting regulation, documentation methods etc. With the completion of this course the candidate gets to select from varied work areas of the industry/sector of his/her interest. Knowing all theoretical and practical facts about post marketing surveillance, candidate feels comfortable and confident when working in the industry. Obviously experience has no match and thus efforts are made to bring in experienced professionals to present projects, take lectures and thus add to the benefits reaped from the course. Same is true for the professionals who are already a part of the CR industry but are keen on making lateral movement in their company by shifting to other Pharmacovigilance Department.

For further enquiries or Prospectus, write to or call us on:

info@igmpiindia.org/+91 8130924488

Aligning Drug Safety and Regulatory Compliance with Argus Safety Software

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