Bundle of video lessons on some additional topics listed below


Please Note:  These video lessons will soon be presented as individual lessons in a new format.  Till that time, please access these videos from this bundle. 


Contract Research Organization (CRO)
Aggregate Reporting
Sponsor
DSUR Content
Data Safety Monitoring Board
GVP Module VI - Part 2
GVP Module VI - Part 1
GVP (Guideline on Good Pharmacovigilance Practices)
Schedule Y
Case Narrative
Central Monitor
Centralized Monitoring
Clinical Research Coordinator (CRC)
Careers in Pharmacovigilance / Drug Safety
Edit Check Preparation
Argus Safety System
REMS Vs RMP
Types of ADRs
Database Creation

CRF (Case Report Form) Creation
DMP (Data Management Plan)
CDM (Clinical Data Management)
E2BR3
Role of Ethics Committee in Clinical Research
Phases of Clinical Trial
DSUR Vs PSUR
Drug Dependence Vs Drug Addiction
Drug Misuse Vs Drug Abuse
MedWatch Forms
Severe Adverse Event Vs Serious Adverse Event

Testimonials

Comments from the students/learners who have benefitted from our learning content

your videos helped me to get a job as a case handler two years ago! Now, I love the field and am being trained as a Domain specialist for IT teams! thank you!


on Youtube

Mam, it was really difficult to understand by own but your video makes very easy to understand and remembering about GVP and other topic that are you discussed. Thankyou so much mam for making videos and request for making more ... Its truly appreciable efforts from your side.

on Youtube


OMG this is one of the best videos i have seen on trial overview. I am not a medical or research person but working for a pharmaceutical company and wanted an overview. You explained it very well. Thanks a bunch


on Youtube