FDA Investigator Joanne Pryzbylik
Joanne Pryzbylik has conducted inspections on 6 sites in 2 countries as of 06 Oct 2008. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
6
Last Inspection Date:
06 Oct 2008
Investigator Role:
FDA Investigation Participant
Redica ID:
Countries of Inspections:
United States of America,
United Kingdom of Great Britain and Northern Ireland
FDA Investigators that have inspected at least one site in common with Joanne Pryzbylik:
Althea A Williams,
Ana S Cabrera,
Ann Marie Montemurro,
Ann Marie Schofield,
Annemarie Bodnar,
Annette A Ragosta,
Arie C Menachem,
Brentley S Collins,
Burnell M Henry,
Byungja E Marciante,
Christian D Lynch (CDL),
Christina H Owens,
Creighton T Tuzon,
Cynthia Jim, CSO,
Dawn L Wydner,
Derek C Price,
Eliezar Ramos,
Eural E Porter,
Fulton A Varner,
Gene D Arcy,
Helen B Ricalde,
Helen R Bester,
J David Doleski,
Jacqueline Mdiaz Albertini,
Jean M Kelahan,
Jennifer Macmillan,
Joan A Loreng,
Julie D Bringger,
Karen A Coleman,
Kelly I Anderson,
Kimberly M Bigler,
Laurel A Beer,
LCDR Debra Emerson,
Marion Michaelis,
Mariza M Jafary,
Martha T Olone,
Mary T Carden,
Meihong Liu,
Michele L Forster, PhD,
Mihaly S Ligmond,
Nawab A Siddiqui,
Omotunde O Osunsanmi,
Patricia F Hudson,
Paul A Bonneau,
Paul W Moy,
Paula A Trost,
Prabhu P Raju,
Qiao Y Bobo,
Richard D Manney,
Rose Ashley,
Sarah Forney,
Sheryl A Kochman,
Shwnji Susie Lee,
Simone E Pitts,
Stephen D Brown,
Susan M Jackson,
Susan Yu,
Teresita C Mercado
Joanne Pryzbylik's Documents
Publish Date | Document Type | Title |
---|---|---|
July, 2001 | EIR | Ortho-Clinical Diagnostics, Inc. - EIR, 2001-07-27 |
August, 2003 | FDA 483 Response | Ortho-Clinical Diagnostics, Inc. - Form 483R, 2003-10-28 |
January, 2008 | FDA 483 | Immucor Inc - Form 483, 2008-01-17 |
July, 2001 | FDA 483 | Ortho-Clinical Diagnostics, Inc. - Form 483, 2001-07-27 |
August, 2002 | FDA 483 | LONZA BIOLOGICS - Form 483, 2002-08-30 |
August, 2003 | EIR | Ortho-Clinical Diagnostics, Inc. - EIR, 2003-08-14 |
November, 2001 | FDA 483 | Immucor Inc - Form 483, 2001-11-15 |
October, 2008 | FDA 483 | ALBA Bioscience Limited - Form 483, 2008-10-13 |
August, 2003 | FDA 483 | Ortho-Clinical Diagnostics, Inc. - Form 483, 2003-08-14 |
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