Streamline Pharmaceutical Manufacturing Processes And Ensure GMP Compliance

Handok Inc. was expanding into the global pharmaceutical market and would be met with an increasing number of compliance requirements. Not only would the organization be subject to global regulations, such as GMP, but it would also be required to prove that it was meeting 21 CFR Part 11 regulations. While the regulations could be met with manual data collection, the process was cumbersome and unreliable.