FDA Investigator Peter Adams, PhD

Peter Adams, PhD has conducted inspections on 2 sites in 2 countries as of 07 Mar 2016. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
2
Last Inspection Date:
07 Mar 2016
Investigator Role:
FDA Investigation Participant
Redica ID:
100008809
Countries of Inspections:
Korea (Republic of), Austria
FDA Investigators that have inspected at least one site in common with Peter Adams, PhD:
Anjali Shukla, PhD, Ashar P Parikh, Bo Chi, PhD, Carla J Lundi, Chiang Syin, PhD, Concepcion Cruz, Jr, Deborah Schmiel, PhD, Dr. Ralph M Bernstein, PhD, Hao Kiet D Phan, Haoheng Yan, PhD, Hyung Yul Lee, Jacek Cieslak, PhD, Jennifer M Gogley, Junho Pak, Justin A Boyd, Kristin M Abaonza, Kurt A Brorson, PhD, Laura Fontan, MS, Linda F Murphy, Maria Joselopez Barragan, PhD, Marion Michaelis, Marjorie A Shapiro, PhD, Maryam Tabatabaie, Matthew B Casale, Michael Shanks, MS, Mra B Kamberem, Patricia F Hughes, PhD, Paul L Bellamy, Reyes Candau Chacon, PhD, Richard Ledwidge (nmi), PhD, Riley C Myers, PhD, Saleem A Akhtar, Scott N Lim, Scott R Nichols, PhD, Stuart W Russell, Thuy T Nguyen, LCDR, Viviana Matta, Wayne E Seifert, William Hallett, PhD, Xiaoping Guan, Zhong Li, PhD

Peter Adams, PhD's Documents

Publish Date Document Type Title
March, 2015 FDA 483 CELLTRION Inc - Form 483, 2015-03-06
March, 2016 FDA 483 Sandoz GmbH - Form 483, 2016-03-11
March, 2015 EIR CELLTRION Inc - EIR, 2015-03-06

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.

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