Charles River Laboratories [Mattawan / United States of America]
Charles River Laboratories [Mattawan / United States of America] located in MATTAWAN MICHIGAN, United States of America had its last known inspection on 19 Jan 2024. There are 20 known inspections on record.
Site Details
Industries:
Medical Devices,
Human Drugs,
Animal Health,
Biologics,
Food and Cosmetics
Tags:
Medical Devices,
Non-Clinical Lab (GLP),
Clinical Bioequivalence or Bioavailability Study,
Animal Health,
Human Drugs,
Biologics,
Analytical Testing,
Food and Cosmetics
Last Inspection Date:
19 Jan 2024
FEI:
1813181
Redica ID:
Investigators:
Barbara A Rusin,
Tracey Asinjen Wiersma,
Xikui Chen (nmi), PhD,
Dina A Tallman,
Nancy A Bellamy,
Douglas W Gronski,
Eric S Pittman,
Byron Ho, DVM,
Dr. Hansong Chen, PhD,
Chelsea W Lamm,
Niraj R Mehta, PhD,
Charles A Snipes, PhD,
Carol Rivera Lopez, PhD,
Dylan D Yao, MD, PhD,
Corey K Reno,
Natalie A Mickelsen, DVM,
Dr. Zhou Chen (nmi), MD PhD,
Gajendiran Mahadevan, PhD,
Dr. Mark J Seaton, PhD,
Dawn C Olenjack,
Joseph R Haynes,
Michael F Skelly, PhD,
William D Tingley,
Sripal R Mada, PhD,
Andrea A Branche
Charles River Laboratories [Mattawan / United States of America]'s Most Recent Documents
Publish Date | Document Type | Title |
---|---|---|
July, 2021 | EIR | Charles River Laboratories - EIR, 2021-07-16 |
March, 2019 | EIR | Charles River Laboratories - EIR, 2019-03-08 |
June, 2018 | EIR | Charles River Laboratories - EIR, 2018-06-28 |
April, 2016 | FDA 483 | Charles River Laboratories - Form 483, 2016-04-15 |
April, 2016 | EIR | Charles River Laboratories - EIR, 2016-04-15 |
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.
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