Pharmaceutical Documentation

13 November 2018, Reading, United Kingdom


Introduction
Course Overview

Documentation is the cornerstone of any company’s quality management system and is an essential GMP requirement. It is critical that anyone dealing with GMP documents and documentation systems understand the regulatory requirements and adopts best practice. As such this course provides a step by step explanation of what to do when managing GMP documentation and documentation systems.

Suitability

This course is appropriate to a wide ranging audience, from QA and QC, through to production and clinical trials professionals.

Learning Outcomes

By the end of the course you will:
  • Understand the GMP rules and guidelines associated with the preparation, completion and archiving of documentation
  • Appreciate the importance of maintaining a comprehensive documentation system
Speakers
Venue
Reading Scientific Services Limited (RSSL)

RSSL Training Suite, Reading Scientific Services Limited (RSSL), Reading Enterprise Centre, Earley Gate, Whiteknights Road, Reading, RG6 6BU, United Kingdom

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