This webinar will explain the basic principles of SOPs and Documentation required for the successful and compliant function of a quality system in the pharma and medical device industries. Particular emphasis will be the specific requirements set out in 21 CFR Part 210/211/820 and how these requirements can be met.
You will learn the current industry standards for creating and maintaining SOPs and documentation in compliance to GMP requirements.
Areas Covered in the Session :
SOP and documentation requirements
SOP and document archiving
SOP creation and obsoletion traceability
Interactive Q&A Session
Who Will Benefit:
Quality Control Departments
Quality Assurance Departments