Webinar on SOPs and Documents

Description :

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

Training requirements

SOP and document archiving

SOP creation and obsoletion traceability

Interactive Q&A Session

Who Will Benefit:

Quality Control Departments

Quality Assurance Departments

Production Departments

Purchasing Departments

Operations Departments

HR Departments