PharmD Info

A forum for Indian Pharmacy Professionals

Important: Registered today to have the complete access on this forum --- Register Here
Its an open online group forum for the Indian Pharmaceutical Regulatory Affairs DRA professionals to discuss and exchange knowledge through various forum topics. Members are authorized write any review topics, questions and create polls. We invite all the Indian DRA professionals to join with us as an active member of this forum.
Forum rules: Forum rules: Dear User, Kindly read our forum rules before you proceed with our PharmD Info, Your first 5 posts/topics requires moderator approval and this website is purely meant for educational and knowledge sharing purpose only so you should not make any topics/replies/messages which criticize, threaten or abuse any member, pharmacy governing bodies and organizations. Your post will be deleted automatically by our BB Pruning System if your topic is not viewed by members for more than 5 days. So, make sure that your topics and its related contents are unique and valuable. We expect you to be an active member of our forum to continue with your free membership.Kindly note that if a member received more than five warnings from moderator/members they will be blocked automatically by our Bulletin Board system.
  • User avatar
#2256
A drug regulatory affair is a dynamic, rewarding field that includes both scientific and legal aspects of drug development. DRA professionals are dedicated individuals who take pride in their contribution to improving the health and quality of life of peoples. RA as profession is broader than registration of products, they advise companies both strategically and technically at the highest level. Their role begins right from development of a product to making, marketing and post marketing.

Regulatory Affairs professionals help the company avoid problems caused by badly kept records, inappropriate scientific thinking or poor presentation of data. In most product areas where regulatory requirements are imposed, restrictions are also placed upon the claims which can be made for the product on labeling or in advertising.

Their role begins right from development of a product to making, marketing and post marketing. Regulatory Affairs professionals help the company avoid problems caused by badly kept records, inappropriate scientific thinking or poor presentation of data. In most product areas where regulatory requirements are imposed, restrictions are also placed upon the claims which can be made for the product on labeling or in advertising.
Similar Topics
Topics Statistics Last post
Hiring for Regulatory Affairs Specialist
by Admin  - 13 May 2017, 08:23  - In: M Pharm Jobs
0 Replies 
912 Views
by Admin
13 May 2017, 08:23
0 Replies 
1066 Views
by Admin
17 May 2017, 10:30
0 Replies 
733 Views
by Admin
15 Jun 2017, 15:04
6 Replies 
4019 Views
by realcarelifesciences
21 Apr 2018, 11:09
0 Replies 
835 Views
by Admin
20 Mar 2017, 18:47

Tags

PharmD Info Online Group Discussion Disc[…]

The Pharmacy Council of India (PCI) has launched a[…]

Indian Association of Colleges of Pharmacy. A/C N[…]

PCI chalks out plans to allay concerns of educatio[…]

WELCOME TO OUR E-LEARN COURSE WORK MODULES