FDA Policy for REMS Reqmts during COVID-19

Health Care, Pharma Industry, Strategic Planning

FDA is issuing this guidance to communicate its temporary policy for certain risk evaluation and mitigation strategies (REMS) requirements for the duration of the coronavirus pandemic public health emergency.

Read the Policy now

 

 

Related Education Resources.

All Resources

Value-Based Healthcare

Topic: Health Care

Report

Members

Brexit & the future landscape for clinical trial supplies in the UK and Europe

Topics: Pharma Industry, Regulatory, Supply Chain

Position Paper

Free

EU Clinical Trial Regulation 536/2014

Topic: Regulatory

Position Paper

Members

Become a member

Global Clinical Supplies Group

Join GCSG for full access...

to our educational resources, conference materials and our directory of more than 480 Clinical Supply colleagues. Experience the culture of collaboration, It only takes approximately 3 minutes 22 seconds.

Please note that membership is included and FREE of charge when you sign up for an event.