FDA Investigator Rosa J Motta
Rosa J Motta has inspections in 7 countries as of 22 Sep 2023. Rosa J Motta has collaborated with a combinined 853 experts on various inspections, contributing to compliance and improvement across diverse sectors.
Investigator Details
Number of Inspected Sites:
10
Last Inspection Date:
22 Sep 2023
Investigator Role:
FDA Investigator
Redica ID:
Country:
Malta,
Spain,
United States of America,
Italy,
Sweden,
France,
United Kingdom of Great Britain and Northern Ireland
Co-Investigator(s):
Adalberto Cajigas,
Alicia M Mozzachio,
Anita R Michael,
Ariel Cruz Figueroa,
Arlene M Badillo,
Cassandra L Abellard,
CDR Ileana Barreto Pettit,
Cody D Rickman,
Diane Kelley,
Erika V Butler,
German Rivera,
Helen B Ricalde,
Heriberto Negron Rivera,
Javier E Santos,
Jorge L Guadalupe,
Jorge L Lajara,
Jose E Melendez, DDC,
Kristy A Zielny,
Laurie B Frazier,
Leonard H Lavi,
Libia M Lugo,
Marian E Ramirez,
Marianela Aponte Cruz,
Maridalia Torres,
Maridalia Torres Irizarry,
Marybet Lopez,
Marybet Lopez Negron,
Matthew B Casale,
Matthew R Dionne,
Mra Mcculloughj,
Pal S Mayasandra,
Parul M Patel,
Patrick L Wisor,
Rajiv R Srivastava,
Ramon A Hernandez,
Raphael E Brykman,
Rebecca Parrilla,
Rebecca Rodriguez,
Richard J Friedman,
Rose J Motta,
Simone E Pitts,
Steven B Barber,
Steven D Kehoe,
Susan D Yuscius,
Victor J Gangi,
William D Tingley,
Youmin Wang
Rosa J Motta's Documents
| Publish Date | Document Type | Title |
|---|---|---|
| June, 2003 | FDA 483 | Dipharma Francis S.r.l. - Form 483, 2003-06-19 |
| October, 2010 | FDA 483 | Synthon Hispania S.L. - Form 483, 2010-10-01 |
| June, 2003 | EIR | Quimica Sintetica S.A. - EIR, 2003-10-16 |
| June, 2003 | FDA 483 | Quimica Sintetica S.A. - Form 483, 2003-06-26 |
| September, 2008 | FDA 483 | Teva Puerto Rico LLC - Form 483, 2008-09-15 |
| February, 2017 | EIR | Mipharm S.p.A. - EIR, 2017-02-03 |
| June, 2003 | FDA 483 Response | Quimica Sintetica S.A. - Form 483R, 2003-06-26 |
| February, 2017 | FDA 483 | Mipharm S.p.A. - Form 483, 2017-02-03 |
| October, 2010 | EIR | Synthon Hispania S.L. - EIR, 2010-10-01 |
Experience Redica System's 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.
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