SOPs as part of the company`s regulatory infrastructure
SOPs and their relation to the regulations
Risk Based approach on SOP Best Practices for creation and maintenance
SOP on SOPs and how to ensure conciseness, consistency and ease of use
Tools for SOP tracking and when is validation required
Training on SOPs
What the FDA looks for in SOPs during an inspection
Who should Attend
Senior attendees from:
Clinical Affairs
Regulatory Affairs
Compliance
Quality Assurance/Quality Control
Manufacturing and Technical Services
Marketing & Sales
IT/MIS
Engineering
Laboratory Operations
Executive Management
Clinical Research managers and personnel
Customer Service
QA/RA managers and personnel
Specialists/SMEs in all departments
Distributors/Authorized Representatives
Quality System auditors
Consultants
Legal Counsel
Past Events
Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs) 2016 - 12-13 May 2016, Hilton Garden Inn Philadelphia Center City, Pennsylvania, United States (58501)
Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs) 2026
Important
Please, check "Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs)" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Healthcare, Medical device, Medical laboratories, Pharma
