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.