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Event :Surviving an FDA Sponsor Inspection - Training for Success

Date :Tuesday February 19th, 2019

Location :Palo Alto
2479 East Bayshore Road,
Suite 200
94303 Palo Alto, United States

Type :Conference & Seminar - International audience

Accreditation :--


Further information


This training program will review a case study derived from actual inspections wherein FDA performed a sponsor site inspection having already audited three of the investigator sites. FDA was aware from these site audits of potential serious noncompliance issues. The course will also discuss Sponsor/CRO/investigator relationship issues from these three site audits.


The sponsor clinical operations staff guided the sponsor and investigator site staff through the FDA inspection/audit process. The result was a passed FDA sponsor inspection and approved NDA. There were no FDA warning letters issued to any investigators.

This webinar will discuss how seemingly insurmountable obstacles to a successful FDA sponsor inspection were resolved and how you can apply these lessons to your next FDA sponsor inspection


  • FDA inspectional procedures; What sponsor staff are audit targets and how FDA inspections are performed
  • Sponsor SOP and TMF options that work and do not work toward complying with FDA documentation requirement
  • FDA sponsor inspection objectives and perspectives
  • Typical and common FDA questions and how not to respond
  • The impact of CRO contractual delegation of project responsibilities on sponsor regulatory obligations
  • Audit of sponsor records and training of sponsor staff as a positive step in preparing for the inspection


Map and directions
Conference address :
Palo Alto
2479 East Bayshore Road,
Suite 200
94303 Palo Alto
United States
tel : +1-888-717-2436
Map and directions

Further information

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Surviving an FDA Sponsor Inspection - Training for Success Hospital - Management
fda sponsor inspection training program, sponsor sop and tmf options, cro contractual delegation, fda sponsor inspectional procedures
Professionals, CQA Regulatory personnel Clinical operations, CRA Director and upper level pharma research management Investigators and research management staff Clinical Project Manager Regulatory Affairs Compliance Manager Trial Master File Manager
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For more information on Surviving an FDA Sponsor Inspection - Training for Success, plsase contactr ComplianceOnline

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