MERCK SERONO SA [Corsier-Sur-Vevey / Switzerland]

MERCK SERONO SA [Corsier-Sur-Vevey / Switzerland] located in CORSIER-SUR-VEVEY VAUD, Switzerland under the [Merck KGaA] organization had its last known inspection on 18 Jan 2024. There are 15 known inspections on record.

Site Details

Industries:
Human Drugs
Tags:
Human Drugs, API Manufacturer, Analytical Testing, FDF Manufacturer
Parent Organization:
Merck KGaA
Last Inspection Date:
18 Jan 2024
FEI:
3003131678
Redica ID:
100316676
Investigators:
Cynthia Jim, CSO, James I Giefer, Omotunde O Osunsanmi, Gerald B Seaborn, Jr, Vaishali J Patel, Barbara Janine Breithaupt, Dennis Cantellops Paite, Scott R Nichols, PhD, Junho Pak, Rose Ashley, Santos E Camara, Reyes Candau Chacon, PhD, Katherine Szestypalow, Steven Fong, MS, PhD

MERCK SERONO SA [Corsier-Sur-Vevey / Switzerland]'s Most Recent Documents

Publish Date Document Type Title
April, 2023 FDA 483 MERCK SERONO SA - Form 483, 2023-04-06
June, 2011 EIR MERCK SERONO SA - EIR, 2011-06-09
June, 2011 FDA 483 MERCK SERONO SA - Form 483, 2011-06-09

Experience Redica Systems’ NEW site dashboards and profiles

Redica Systems customers can leverage the full Quality and Regulatory Intelligence suite, with powerful analysis covering thousands of sites around the world. You can search by FEI, or more powerfully, by the Redica ID, our universal identifier for global life sciences manufacturing sites, an industry first.

Investigator Profiles are not sold as on-demand documents. If you’d like to see one, fill out the form below to connect with our Sales Team and get it in your inbox as little as 24 hours.

Site Profile Icon

Loading...

Site Profiles Are Just the Tip of the Iceberg

Becoming a Redica Systems customer not only provides you with unlimited access to our extensive inventory of site profiles, but also grants you access to:

Inspection Intelligence

  • Pre-Approval Inspection (PAI) trends
  • The ability to filter nearly any FDA enforcement action by GxP labels like GMP, GCP, etc.
  • Latest 483s: see what the trends are across all FDA Investigators
  • CFR Heatmap: Citations aggregated by Subpart by Year

Vendor Intelligence

  • Full inspection histories for your vendors down to the specific site level
  • All of the functionality mentioned above but isolated to just your vendors

Regulatory Intelligence

  • Zero in on the trends for a specific agency/regulator (ex. FDA, MHRA, EMA, Health Canada)
  • All the latest "Signals" from agencies around the world, segmented by Country, Type (ex. Guidance, Decree...), Category (ex. Rules/Regulations/Guidance, News, Reports...), Theme (ex. Cell and Gene Therapy, AI...), and more