FDA Investigator Henry E Sanchez

Henry E Sanchez has inspections in 2 countries as of 25 Aug 2023. Henry E Sanchez has collaborated with a combinined 1363 experts on various inspections, contributing to compliance and improvement across diverse sectors.

Investigator Details

Number of Inspected Sites:
50
Last Inspection Date:
25 Aug 2023
Investigator Role:
FDA Investigator
Redica ID:
Country:
United States of America, Canada

Henry E Sanchez's Documents

Publish Date Document Type Title
January, 2000 FDA 483 Giles, Thomas D, M.D. - Form 483, 2000-01-31
March, 2001 EIR Mylan Pharmaceuticals ULC - EIR, 2001-05-24
December, 2002 FDA 483 Southern Transplant Service Inc - Form 483, 2002-12-11
March, 2001 FDA 483 Response Mylan Pharmaceuticals ULC - Form 483R, 2001-03-09
February, 2002 EIR Beck, David E., M.D. - EIR, 2002-02-05
January, 2000 EIR Giles, Thomas D, M.D. - EIR, 2000-01-31
November, 2002 FDA 483 The Blood Center - Form 483, 2002-11-18
August, 2001 FDA 483 Clisham, P. Ronald, MD - Form 483, 2001-08-15
November, 2002 FDA 483 Response The Blood Center - Form 483R, 2002-12-04
August, 2001 EIR Clisham, P. Ronald, MD - EIR, 2001-08-15

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