Good Documentation Practices for the Laboratory

According to the FDA, if it isn’t written down, it didn’t happen. As well, if it isn’t written down clearly, it didn’t happen either. GMP compliance requires the use of good documentation practices (GDP). These practices apply to all pharmaceutical manufacturing and support areas. GDP defines the required activities and steps to use when recording data and other handwritten entries. Personnel who work with documentation must be informed of these requirements, recognize their significance to their job and be aware of the consequences of non-compliance. During this webinar, you will review agency and industry standard expectations of Good Documentation Practices plus see examples of these practices (both good and bad!) as they apply to the pharmaceutical laboratory.