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2020 - Designing and Sustaining New and Existing Product Stability Testing Program
Date2020-06-18 - 2020-06-19
Deadline2020-06-08
VenueVirtual Seminar, USA - United States 
KeywordsDocumentation Methods; Analytical Testing Considerations; FDA's Drug Stability Testing Program
Topics/Call fo Papers
Quality Control Analyst and Management
Senior Management
Manufacturing Associates and Management
Shipping and Distribution Personnel
Stability Testing Department Personnel and Management
Regulatory Affairs
Quality Assurance Analyst and Management
Process Design Personnel and Management
Drug Packaging Personnel and Management
Senior Management
Manufacturing Associates and Management
Shipping and Distribution Personnel
Stability Testing Department Personnel and Management
Regulatory Affairs
Quality Assurance Analyst and Management
Process Design Personnel and Management
Drug Packaging Personnel and Management
Other CFPs
- Quality Control Laboratory Compliance - cGMPs and GLPs
- Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions
- Navigating through Maze of In-vitro Diagnostics (IVD) Regulations: A systematic approach from Regulatory Strategy to Regulatory Approvals in U.S./Europe/Canada
- REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance
- Project Management for Human Resources
Last modified: 2020-05-18 18:23:38