FDA Investigator Christopher A Demitrius
Christopher A Demitrius has inspections in 3 countries as of 11 Oct 2023. Christopher A Demitrius has collaborated with a combined 840 experts on various inspections, contributing to compliance and improvement across diverse sectors.
Investigator Details
Number of Inspected Sites:
14
Last Inspection Date:
11 Oct 2023
Investigator Role:
FDA Investigator
Redica ID:
Country:
United States of America,
Italy,
Germany
Co-Investigator(s):
Abby E Pelletier,
Allison A Rodriguez,
Alysia M Salonia,
Bonnie E Conley,
Christina L Bigham,
Christine E Kelley,
Cynthia T Cain,
Darin S Wiegers,
David P Vanhouten,
Evelyn Taha,
Garry H Stewart,
George T Allen, Jr,
Gina M Brackett,
Harperd,
Jacqueline S Warner,
Jamie S Mathews,
Jay M Patria,
John A Sciacchitano,
John P Shelton,
Joyce A Williams,
Kathleen M Curry,
Lauren M Lawrance,
Laurie B Frazier,
Lori A Lahmann,
Maribeth G Niesen,
Mark E Farrell,
Mark E Parmon,
Martin J Guardia,
Maryam Tabatabaie,
Megan A Haggerty,
Michelle M Noe,
Monica J Wilkins,
Mutahar S Shamsi,
Nichole B Murphy,
Osama A Khatib,
Pamela L Ogonowski,
Rebecca A Coleman,
Richard F Hapke,
Robert Sharpnack,
Roy C Stephens,
Rupa Pradhan,
Stephen C Smith,
Stephen D Eich,
Sunita Pandey,
Teddy Tom,
Teresa K Kastner,
Terry C Kimball,
Thomas W Nerney,
Timothy M Glod
Christopher A Demitrius's Documents
Publish Date | Document Type | Title |
---|---|---|
January, 2001 | FDA 483 Response | Meridian Bioscience Inc - Form 483R, 2001-02-09 |
August, 2001 | EIR | Beaver Visitec - EIR, 2001-08-02 |
January, 2001 | FDA 483 | Meridian Bioscience Inc - Form 483, 2001-01-17 |
October, 2002 | FDA 483 | Tecres S.p.A. - Form 483, 2002-10-03 |
October, 2002 | EIR | Tecres S.p.A. - EIR, 2002-10-03 |
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](https://redica.com/document-store/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