FDA Investigator Ching Jeyg Chang
Ching Jeyg Chang has conducted inspections on 3 sites in 1 countries as of 28 Mar 2016. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
3
Last Inspection Date:
28 Mar 2016
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with Ching Jeyg Chang:
Andria L Kuhlman,
Anna M Brannen,
Christopher T Middendorf,
Dell S Moller,
Donna F Campbell,
Dr. Abhijit Raha, PhD,
Dr. Cj George Chang,
Dr. Mark J Seaton, PhD,
Dr. Zhou Chen (nmi), MD PhD,
Geoffrey K Kilili,
Hugh M Mcclure, II,
James P Mcevoy,
Jennifer L Jager,
Kathryn Suttling,
Kristina J Donohue,
Laine P Myers,
Marcelo O Mangalindan, Jr,
Marcia A Worley,
Mike M Rashti,
Phillip M Pontikos,
Richard W Berning,
Rosanna M Goodrich,
Tahseen Mirza,
Thunder N Dunkijacobs,
Vlada Matusovsky,
Yvette Mlacour Davis
Ching Jeyg Chang's Documents
Publish Date | Document Type | Title |
---|---|---|
March, 2016 | FDA 483 | GlaxoSmithKline LLC - Form 483, 2016-03-18 |
April, 2016 | FDA 483 | StageBio - Form 483, 2016-04-01 |
April, 2016 | EIR | StageBio - EIR, 2016-04-01 |
March, 2016 | EIR | GlaxoSmithKline LLC - EIR, 2016-05-03 |
Experience Redica Systems’ NEW investigator profiles and dashboards
Redica Systems customers get access to over 1,400 FDA Investigator profiles, containing powerful analysis like:
- Total inspections conducted
- 483 rate
- OAI rate
- Warning Letter rate
- Inspections by Industry, Scope, and Inspection Reason
- And much more
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.
![FDA Investigator Profile Icon](/images/InspectorProfile.png)
Talk to sales to access our investigator profiles
Loading...
Investigator Profiles Are Just the Tip of the Iceberg
Becoming a Redica Systems customer not only provides you with unlimited access to profiles similar to the one above for every current and former FDA Investigator, 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