Skip to main content
The drug industry's voice for manufacturing excellence
Production
Development
Information Technology
Compliance
Quality & Risk
Sections
Production
Development
Information Technology
Compliance
Quality & Risk
Facilities
Sectors
Special
Webinars
Podcasts
E-Handbooks
Industry News
Magazine Archives
Contact
Newsletter Subscription
Contact Us
Advertise
Follow us on
https://www.facebook.com/pages/Pharmaceutical-Manufacturing/140261116014887
http://www.linkedin.com/groups?gid=1813799
http://twitter.com/PharmaMfg
cGMPs
Afnan to FDA: Simplify Post-Approval Changes, Spur Innovation
21 CFR 314.70, and the process by which FDA reviews changes to already approved applications, needs a risk-based update, now. Consultant Ali Afnan, formerly with FDA, makes his case.
June 10, 2010
Add Us On Google
Sign up for our eNewsletters
Get the latest news and updates
Sign Up
Related
Sun Pharma invests in new manufacturing facility in India amid FDA scrutiny
Novo Nordisk’s troubled Indiana site hit with Form 483 following FDA re-inspection
Sponsored
2026 Manufacturing Pharma Trends for Life Sciences
Sponsored
2026 AI Trends in Life Sciences
Trending
Cellares, Ori Biotech square off in battle to automate the manufacturing of cell therapies
US biotech leadership at risk as China dominates manufacturing: survey
Lotte Biologics completes construction of South Korean manufacturing plant
Sponsored Picks
Sponsored
Condensate Management in Your Compressed Air System
Sponsored
An Advanced Way to Install a Compressed Air System
Sponsored
The Battle in Your Pipes: Gravity vs Air Velocity in Condensate Mgmt
Load More Content