2021 - Validation Essentials for Medical Device Manufacturers - IQ, OQ, PQ
Date2021-03-16
Deadline2021-03-06
VenueOnline event, USA - United States
KeywordsValidation of medical devices; Quality system regulations; Iq oq pq medical devices
Topics/Call fo Papers
Purpose, scope, and benefits of process validation
FDA Expectations, Regulations
Lessons learned and enforcement case studies
Common problems and easy solutions
When to verify and when to validate
Steps and Checklists for validation
Linkages within your Quality System
Master Validation Planning
Best Practices
Inspection Preparedness
FDA Expectations, Regulations
Lessons learned and enforcement case studies
Common problems and easy solutions
When to verify and when to validate
Steps and Checklists for validation
Linkages within your Quality System
Master Validation Planning
Best Practices
Inspection Preparedness
Other CFPs
- Implementing a Robust Data Integrity Program
- Digital Payments 2021 - The future of Payments
- California Leaves of Absence - Employer Obligations, Leave Interactions, and Handling Problems and Performance Management Challenges - PDL, FMLA, FEHA, SDI, CFRA, PFL, ADA, and Workers Compensation
- Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries)
- Global Regulations for Equipment Qualification and Validation of Processes in the Pharma Manufacturing
Last modified: 2021-02-27 03:38:05