FDA Investigator Edwin Martinez
Edwin Martinez has conducted inspections on 25 sites in 4 countries as of 20 Mar 2017. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
25
Last Inspection Date:
20 Mar 2017
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
China,
Canada,
Puerto Rico,
India
FDA Investigators that have inspected at least one site in common with Edwin Martinez:
Adalberto Cajigas,
Adaliz Santaliz Cruz,
Alan P Kurtzberg,
Alberto A Viciedo,
Anita Narula, PhD,
Ann L Demarco,
Annette Melendez,
Anthony A Charity,
Ariel Cruz Figueroa,
Arlene M Badillo,
Arsen Karapetyan,
Barbara Janine Breithaupt,
Bonita S Chester,
Brenda Rivera,
Carla A Norris,
Carlos A Medina,
CDR Ileana Barreto Pettit,
CDR Thomas R Berry, PPh,
Charles I Ann,
Charles M Edwards,
Chelsea N Sealey,
Cheryl A Clausen,
Christina A Miller,
Claire M Minden,
Dana M Klimavicz,
Daniel L Obrzut,
Dayna I Martinez,
Dewayne E Whitlock,
Djamila Harouaka,
Dr. Sriram Subramaniam, PhD,
Eric S Weilage,
Felix Maldonado,
Frances L Dejesus,
Gam S Zamil,
German Rivera,
Gwyn G Dickinson,
Hector Jcolon Torres,
Iraida Ortiz,
Israel Santiago, OCM,
Ivis L Negron,
James C Maclaughlin,
James S Cartwright,
Jason F Chancey,
Javier O Vega,
Jeffrey P Raimondi,
Jennifer A Quinones,
Jogy George,
John A Gonzalez,
Jorge E Martinez,
Jorge L Guadalupe,
Jorge L Lajara,
Jose A Lopez,
Jose A Moreno,
Jose Acruz Gonzalez,
José E Meléndez,
Jose M Cayuela,
Jose Perez Soto,
Jose R Lopez,
Jose Velez,
Juan Rjimenez Garcia,
Karl D Hezel,
Kent C Faul,
Krishna Ghosh, PhD,
Kshitij A Patkar,
Laiza V Garcia,
Lareese K Thomas,
Lata C Mathew, PhD,
Laura E Garcia,
Lauren N Howard,
Laurimer Kuilan Torres,
Libia M Lugo,
Lisa M Lopez,
Lourdes Andujar,
LT Rafael Gonzalez,
Luis Soto Lopez,
Marian E Ramirez,
Marianela Aponte Cruz,
Marijo B Kambere, PhD,
Marlene Rodriguez Colon,
Martin K Yau, PhD,
Mary E Storch,
Michael R Goga,
Michael R Klapal,
Michelle Yclark Stuart,
Miguel A Martinez Perez,
Miguel Hernandez Sanchez,
Milva E Melendez Perales,
Min Tang,
Minerva Rogers,
Muralidhara B Gavini, PhD,
Myriam M Sosa,
Nancy Rosado,
Nebil A Oumer,
Nicole E Knowlton,
Nilufer M Tampal, PhD,
Noreen Muñiz,
Pablo Feliciano,
Patrick C Klotzbuecher,
Patrick L Wisor,
Peter E Baker,
Pratik S Upadhyay, DDC,
Rafael E Cruz,
Rafael Nevarez Nieves,
Ramon A Hernandez,
Rapti D Madurawe,
Raquel Gonzalez Rivera,
Raymond T Oji,
Rebeca M Melendez,
Rebecca Parrilla,
Rebecca Rodriguez,
Regina T Brown,
Robert J Martin,
Robin P Mathew,
Rochelle L Cross,
Russell K Riley,
Santos E Camara,
Sarah E Mcmullen,
Sarah Forney,
Shirley H Isbill,
Sixto M Mercado Rios,
Sonia M Monges,
Sony Mathews,
Stephen J Mottola,
Steven A Brettler,
Steven B Barber,
Susan F Laska, MS,
Temar Q Williams,
Thomas J Arista,
Truong Xuan Nguyen (Andy),
Ucheabuchi Cchudi Nwankwor,
Victor S Pacheco,
Vilmary Negron Rodriguez,
Wanda J Torres,
Wayne D Mcgrath,
Yifan Wang,
Ying Zhang,
Yvette I Henry,
Yvette I Johnson,
Zhao Wang, PhD,
Zhongren Wu
Edwin Martinez's Documents
Publish Date | Document Type | Title |
---|---|---|
March, 2017 | FDA 483 | Ex-Lax, Inc. - Form 483, 2017-03-31 |
June, 2009 | FDA 483 | Wyeth Parenterals Divison of Wyeth Holdings Corp. - Form 483, 2009-06-29 |
October, 2012 | FDA 483 | Caribe Holdings (Cayman) Co.ltd. DBA PuraCap Caribe - Form 483, 2012-10-22 |
September, 2007 | FDA 483 | Bristol-Myers Squibb Holdings Pharma, Ltd. Liability Company - Form 483, 2007-09-07 |
April, 2002 | EIR | Wyeth Pharmaceuticals Company - EIR, 2002-04-04 |
February, 2005 | FDA 483 | McNeil Healthcare LLC. - Form 483, 2005-02-23 |
April, 2002 | FDA 483 | Wyeth Pharmaceuticals Company - Form 483, 2002-04-04 |
February, 2005 | EIR | McNeil Healthcare LLC. - EIR, 2005-02-23 |
November, 2002 | EIR | Neopharm Labs Inc - EIR, 2005-03-25 |
October, 2012 | EIR | Caribe Holdings (Cayman) Co.ltd. DBA PuraCap Caribe - EIR, 2012-10-22 |
August, 2009 | FDA 483 | Agropharma Laboratories Inc. - Form 483, 2009-08-19 |
February, 2004 | EIR | Knoll LLC - EIR, 2004-02-06 |
February, 2004 | FDA 483 | Knoll LLC - Form 483, 2004-02-06 |
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.
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