See how easy it is to set up an eTMF and manage regulatory documents in Egnyte.

See why having document controls is not only essential from a legal perspective, but it is also beneficial.

Learn how data sampling plays a crucial role in determining the validity of an outcome in statistical analysis.

David Grote from Immunocore discusses how emerging biotechs can mature in a GxP compliant manner.

See how audit trails play a crucial role in security and compliance, as well as help troubleshoot and optimize operational systems.

Learn why a Validation Master Plan, though not explicitly required, provides a useful framework for creating the documentation required by the FDA.

Learn how the HIPAA Security Rule, focused explicitly on electronic protected health information (ePHI), drives profitability and differentiation.

Learn how the HITECH Act helped improve the healthcare system by giving significantly more enforcement power to HIPAA and expediting EHR adoption.

Learn about Good Pharmacovigilance Practices, and how they enable pharmaceutical companies to help prevent harm to humans caused by adverse drug reactions.

Learn about Good Manufacturing Practice, a set of general principles that helps organizations drive the most effective and efficient quality process.