When your laboratory or company advances from R&D to manufacturing a pharmaceutical product, food, medical device, or any other product intended for human or veterinary use, you will inevitably hit the requirement to comply with the GxP guidelines. GxP is a general abbreviation for the "good practice" quality guidelines and regulations. The "x" represents a particular field, such as laboratory (GLP), manufacturing (GMP), clinical (GCP), etc.
The transition to the regulated environment can be a challenging task. Not only does it require significant financial investment, but it also presents a huge bureaucratic burden for the organization.
Download this guidebook to learn the technical features an electronic lab notebook (ELN) needs to have to help you mitigate the many hurdles related to documentation management in GMP and GLP environments.
