2020 - Managing Domestic and Foreign FDA Inspections and the COVID-19 Impact
Date2020-06-18 - 2020-06-19
Deadline2020-06-08
VenueVirtual Seminar, USA - United States
KeywordsFDA inspection seminar; FDA 483; FDA warning letter
Topics/Call fo Papers
FDA legal authority to inspect
Over products
Over firm’s
Scientific/clinical studies
Premarket requirements
Postmarket requirements
FDA’s annual inspection work plan
Inspection Procedures
FDA inspection Manuals
FDA Training
Documenting violations
Refusals
Human factors
Recall procedures (What FDA expects from you.)
FDA Field Office Management
FDA Center(s) Management
The firm’s job
Inspectional observations (Form FDA-483)
Responding to a 483
Responding to a Warning Letter
FDA enforcement actions
Follow up inspections
Foreign Inspections
Over products
Over firm’s
Scientific/clinical studies
Premarket requirements
Postmarket requirements
FDA’s annual inspection work plan
Inspection Procedures
FDA inspection Manuals
FDA Training
Documenting violations
Refusals
Human factors
Recall procedures (What FDA expects from you.)
FDA Field Office Management
FDA Center(s) Management
The firm’s job
Inspectional observations (Form FDA-483)
Responding to a 483
Responding to a Warning Letter
FDA enforcement actions
Follow up inspections
Foreign Inspections
Other CFPs
- How to Conduct an ACH Risk Assessment and Develop an Effective ACH Risk Management Program
- Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR
- 21 CFR Part 11 Compliance for SaaS/Cloud Applications
- REACH and RoHS Compliance: Gain a Deeper Understanding
- REACH and RoHS Compliance: Gain a Deeper Understanding
Last modified: 2020-05-02 22:39:50