Drug Safety Associate Training Program & Job Placement

Company Description: We are based at Research Triangle in North Carolina. An established Clinical Research and Information Technology consulting and management firm.

We are specialized in providing in consulting and manpower support to the clinical research and drug development processes solutions for Phase I to phase IV clinical trials as well as post marketed drug products to the Pharmaceutical, Biomedical and Site management companies.

We are determined and dedicated for high quality consulting services with superb efficiency to our healthcare and pharmaceutical clients and partners. We provide professional training, prepare the candidates and successfully do the job placement. We have various training program for you.

Our Faculties: Professionally qualified with MD and PhD degrees, who have over decades of working experience in American Pharmaceutical Companies, USA Federal Government Institute, University and Medical Institute.

Drug Safety/Pharmacovigilance Training Course Description:   We will provide materials and demonstration for the Pharmacovigilance function and principles. In this program candidates not only get the fundamental understanding of the Pharmacovigilance in the drug development process we also prepare you to do the day to day hands on responsibilities of the position. Training includes clinical data practice; serious adverse event data processing; coding of medical history, events and drugs; case narrative writing; data reporting-management and safety case review etc.

Who Should Attend? Bachelors or Masters Degree in any Bio or Life sciences, BPharm/MPharm/PharmD, MBBS, BDS, RN, OT/PT, MD or Postdoctoral Fellows.

Demo for the Training: We have scheduled FREE demo for Drug Safety Training Program every weekend. Please call or email to attend FREE demo.

Course Content for Pharmacovigilance Training:

Introduction to clinical research: Fundamentals and basics of Pharmacovigilance

Clinical Trials: Collection of Safety Data and Establishing the Adverse Drug Reaction Profile

Clinical Laboratory Safety Data in Drug Studies

Ethical Issues in Drug Safety

Operational aspects of the drug safety function within a pharmaceutical company

Regulations in pharmacovigilance: FDA, EU, ICH, Global regulations

Introduction to safety databases and different types

Serious Adverse events (SAE) and its types

Different types and sources of Adverse events reporting

Regular.