A Pharma Manufacturer’s Guide to Delivering on Current & Evolving GMP, FDA & DQSA Regulations

It’s no secret that till date compliance remains the biggest challenge for the pharmaceutical industry. Adhering to 21 CFR Part 11, GMP, DQSA, and GDPR is non-negotiable. This calls for ensuring a 100% traceability of raw materials, strips, and bottles back to the supplier and keeping a log of every transaction that occurs during procurement, manufacturing and distribution.



Digitizing warehouse operations is fundamental now. It helps secure documentation for evolving regulations, tracking products through complex supply chains, comply with drug storage regulations and drive accurate serialization.



Download this eBook and explore how an advanced WMS empowers pharma companies to:



  • Achieve granular inventory control to comply with 21 CFR Part 11
  • Generate highly accurate serial numbers at to adhere with DQSA
  • Digitize documentation to ease FDA audit processes and adhere to cGMP



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