The compliance process at pharmaceutical manufacturers is complicated because many still use paper-based systems to record manufacturing steps. These paper records are reviewed by FDA auditors to ...

Typical Elements Required to be Included in the Batch Production Record and the Device History Record in order to Accomplish a Quality and Cost Effective Review and Quality Assessment based on current ...

InstantGMP Named #1 for EBR, LIMS & MES Integration Being recognized by Root Analysis as the number one provider of ...

“It’s a privilege to be recognized by SafetyCulture as one of the best GMP software providers for 2025,” said Dr. Richard Soltero, President of InstantGMP.” — Dr. Richard Soltero CARY, NC, UNITED ...

Complementary to ERP systems, MES platforms help leaders optimize their production planning as precisely as they do their business operations—and inform better business decisions by enriching records ...