Pharmacovigilance guideline E2B(R3) PART-1
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- Опубліковано 2 бер 2018
- This presentation explains one of the pharmacovigilance guideline that describe about the electronic transmission of ICSR (Individual Case Safety Report).
This presentation explains in very detail about the changes that what they have implemented in this revision. It will be very useful for the people who are working in pharmacovigilance domain.
Great session
Nice sir
Excellent.. 😊 Expecting more videos regarding pharmacovigilance and regulatory.. 😊
Excellent..😊😊
Great good job @Shiva
Great job! Really appreciate it!
Very nice and clean information
Clear and understandable
It's superb.Please make more videos on this.
Superb Siva....
Super sir, please add much on the granular changes in detail...
Kudos...
Good job shiva 👌🏻
Good
Excellent.. can we expect more videos in Aggregate reporting?
Can you take presentation of Good pharmacovigilance practice revision 2.(Module 6)
Do you provide training in ARISg?
If possible plz give a presentation on future of pv in automation
What if difference between E2B,R2 and E2B,R3
Sir can we do diploma in clinical research and pharmacovigilance or should M Pharmacy in pharmacology
Icsr compliance and submission guideline and timeline
Super sir, please add much on the granular changes in detail...
Kudos...