Phishing warning and office closure notice01-May-2024
We are aware of phishing emails targeting speakers of events whose names appear on our events pages. If you are unsure if an email regarding event registration or accommodation has come from us please contact us and do not provide any credit card details or personal information.
The Events Team office will be closed from Thursday 24 December 2025 until Monday 5 January 2026. You can still submit during this period but we will not be available to respond to enquiries or authorise listings until the week of our return.
This course is appropriate to a wide ranging audience, from QA and QC, through to production and clinical trials professionals.
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.
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
