Navitas Life Sciences

Implementing a Regulatory Technology Solution to support DMS, eCTD, and SPL needs

Our client, a mid-sized pharmaceutical company researching and developing novel ophthalmic, ENT, injectables, and over the counter products had experienced rapid growth which had resulted in an increase in patent applications, pipeline and marketed products.

Read our case study and learn how Navitas Life Sciences successfully delivered pharmaREADY DMS, eCTD and SPL modules to meet our clients needs and to ensure 21 CFR Part 11 compliance. Our client is now benefiting from:

  • ~30% time saving for time that would have otherwise been lost in manual searches and processes
  • Streamlined workflow documents
  • Improved in-house productivity
  • Ability to manage M&A and MA transfers
  • Better collaboration
  • Increased savings

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