J&J Pharmaceutical Research & Development, L.L.C. [Raritan / United States of America]
J&J Pharmaceutical Research & Development, L.L.C. [Raritan / United States of America] located in RARITAN NEW JERSEY, United States of America had its last known inspection on 23 Oct 2008. There are 4 known inspections on record.
Site Details
Industries:
Human Drugs
Tags:
Non-Clinical Lab (GLP),
Human Drugs
Last Inspection Date:
23 Oct 2008
FEI:
2246658
Redica ID:
Investigators:
J&J Pharmaceutical Research & Development, L.L.C. [Raritan / United States of America]'s Most Recent Documents
| Publish Date | Document Type | Title |
|---|---|---|
| January, 2004 | FDA 483 | J&J Pharmaceutical Research & Development, L.L.C. - Form 483, 2004-01-23 |
| September, 2002 | EIR | J&J Pharmaceutical Research & Development, L.L.C. - EIR, 2002-09-13 |
| September, 2002 | FDA 483 | J&J Pharmaceutical Research & Development, L.L.C. - Form 483, 2002-09-13 |
| September, 2002 | FDA 483 Response | J&J Pharmaceutical Research & Development, L.L.C. - Form 483R, 2002-09-20 |
| June, 2000 | EIR | J&J Pharmaceutical Research & Development, L.L.C. - EIR, 2000-06-29 |
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