The module will give students extensive training specific to clinical research associate job responsibilities in agreement with the industrial standards. All the necessities of the CRA will be trained and a real-time project or on the job training will also be provided.
Clinical Research Courses In
This module provides an introduction to the clinical research process and its history and development
- Clinical research process
- Planning a clinical trial
- Preparing essential documents: Protocol, CRF, IB, ICD
- EC & Regulatory submission
- Trial Management
- SAE Reporting
Training on Drug Safety. The pharmacological science relating to the collection, detection, assessment, monitoring, and prevention of adverse effects with pharmaceutical products.
- Our training faculty includes academic experts, industry consultants and subject matter experts.
- Flexible learning schedule.
Pharmacovigilance Training in
Program Duration: Two Month, Daily 2Hrs
We do provide Clinical Research, Regulatory Affairs and also Clinical Data Management training with JOB ASSISTANCE
Pharmacovigilance (PV )), also known as drug safety, is the pharmacological science relating to the collection, detection, assessment, monitoring, and prevention of adverse with pharmaceutical products Ultimately, pharmacovigilance is concerned with identifying the hazards associated with pharmaceutical products and with minimizing the risk of any harm that may come to patients.
Module 1 Introduction to Pharmacovigilance
Module 2 Regulatory Guideline in Pharmacovigilance
Module 3 Causality Assessment and Expedited Reporting