Chugai Pharma Manufacturing Co., Ltd [Ukima / Japan]

Chugai Pharma Manufacturing Co., Ltd [Ukima / Japan] located in UKIMA TOKYO, Japan had its last known inspection on 27 Oct 2023. There are 4 known inspections on record.

Site Details

Industries:
Human Drugs
Tags:
API Manufacturer, Human Drugs, Manufacturer, Analytical Testing
Last Inspection Date:
27 Oct 2023
FEI:
3004109596
Redica ID:

Chugai Pharma Manufacturing Co., Ltd [Ukima / Japan]'s Most Recent Documents

Publish Date Document Type Title
August, 2021 FDA 483 Chugai Pharma Manufacturing Co., Ltd - Form 483, 2021-08-23

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