FDA Investigator Dov H Pluznik, PhD

Dov H Pluznik, PhD has conducted inspections on 5 sites in 3 countries as of 09 May 2005. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
5
Last Inspection Date:
09 May 2005
Investigator Role:
FDA Investigation Participant
Redica ID:
100009293
Countries of Inspections:
Puerto Rico, Germany, United States of America
FDA Investigators that have inspected at least one site in common with Dov H Pluznik, PhD:
Adaliz Santaliz Cruz, Alan A Rivera, Andrea George, PhD, Arlene M Badillo, Ashley N Queen, PhD, Astrida B Mattson, Calvin B Koerner, Caryn M Mcnab, Christopher Downey, PhD, Colleen Thomas, PhD, Connie P Rezendes, Dawn E Barkans, Dennis Cantellops Paite, Donald C Obenhuber, PhD, Dr. Zhihao Qiu (Peter), PhD, Eliezar Ramos, Erika V Butler, Gilbert T Salud, Ivis L Negron, Jacqueline Mdiaz Albertini, James I Giefer, Jane M Kreis, Jennifer Lalama, Jerri Baker, Jorge L Lajara, Jose A Lopez, Jose Acruz Gonzalez, José E Meléndez, Jose R Lopez, Jose Velez, June H Wetherington, Kevin D Kallander, Libia M Lugo, Linda S Leja, LT Rafael Gonzalez, Maria Gutierrez Lugo, PhD, Marian E Ramirez, Maxwell Van Tassell, PhD, Michael A Charles, Michael Shanks, MS, Michele Perry Williams, Michelle Yclark Stuart, Mihaly S Ligmond, Milva E Melendez Perales, Myriam M Sosa, Nicholas Obiri, PhD, Nikolay Spiridonov, Noreen Muñiz, Nydia E Colon, Omotunde O Osunsanmi, Patricia F Hughes, PhD, Paul Z Balcer, Paula A Trost, Prabhu P Raju, Ramesh Potla, PhD, Ramon A Hernandez, Rebecca E Dombrowski, Rebecca Parrilla, Rebecca Rodriguez, Riley C Myers, PhD, Robert Darius, S Lori Brown, PhD MPH, Steven C Madzo, Steven Fong, MS, PhD, Susan M Jackson, Thomas J Arista, Timothy Wadkin, PhD, Vilmary Negron Rodriguez, Wendy G Tan, PhD, Zachary L Stamm, Zhong Li, PhD

Dov H Pluznik, PhD's Documents

Publish Date Document Type Title
July, 2001 EIR Immunex Corp. - EIR, 2001-07-09
May, 2005 EIR Amgen Manufacturing Limited LLC - EIR, 2005-05-20
July, 2001 FDA 483 Immunex Corporation - Form 483, 2001-07-09
September, 2001 EIR Aventis Behring Gmbh - EIR, 2001-11-15
January, 2004 FDA 483 Bayer Healthcare aka Berlex Laboratories, Inc. - Form 483, 2004-01-30
May, 2005 FDA 483 Amgen Manufacturing Limited LLC - Form 483, 2005-05-20

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

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