pharmadog
News
when
  • Latest
  • Archive
by source
  • All Sources
  • Sources Page
Jobs
department
  • Clinical
  • Regulatory
  • Medical Affairs
  • Commercial
  • R&D / Discovery
  • Biostatistics / Data
  • Manufacturing / CMC
  • Market Access
therapeutic area
  • Oncology
  • Immunology
  • Neuroscience
  • Cardiovascular
  • Metabolic
  • Rare Disease
  • Infectious Disease
location & type
  • Remote Only
  • US Only
  • California
  • Massachusetts
  • Internships
  • Phase 3 Roles
  • All Jobs →
Sign InSubscribe
pharmadog

fetch the data · sniff the signal

Discover
  • Jobs
  • News
Hubs
  • Topics
  • Patent cliff
  • Publications
Tools
  • Compare
  • Search
  • Bookmarks
Trust
  • About
  • Sources
  • Contact
Legal
  • Privacy
  • Terms
  • Pricing

© 2026 pharmadog.xyz

made by humans and a good dog

  • home
  • jobs
  • news
  • search
raps·23h ago·1 min read
save

EMA says regulators pledge API inspection sharing but report modest progress

Sep 14, 2026·read at raps ↗RegulatoryNeutral

The European Medicines Agency reports that regulators worldwide are strongly committed to sharing plans for good manufacturing practice inspections of active pharmaceutical ingredient suppliers.

Despite this commitment, the sharing of actual inspection reports has only shown moderate progress in recent years.

Joint inspections remain difficult, with the number of such inspections falling by 50% compared to the previous reporting period, underscoring ongoing challenges.

source

This writeup was produced by pharmadog from original reporting by raps.

Original headline: “EMA reports on international API inspection sharing effort”

read at raps ↗
sharex / twitterlinkedin

comments(0)

5-min edit window · permanent after that
sign in to leave a comment · permanent archive after 5 minutes
no comments yet — first sniff?

companies & drugs in this story

no entities indexed yet

related stories

  • 23h agoEMA guideline addresses concerns with potential drug interactions in the GI tractraps
  • 23h agoConvergence 2026: Shaping the next 50 years of regulatoryraps
  • 23h agoRecon: New FDA oncology chief vows continued innovation in OCE; FDA approves drugs for two rare genetic diseasesraps
  • 23h agoAsia-Pacific Roundup: Singapore advances legislation to build ‘more coherent, future-ready’ regulatory systemraps
  • 3d agoThis Week at FDA: Pregnancy exposure registries, PRV fee rates, and moreraps