4.Regulatory Affair

4.2.The power of possibilities

OMIDDAROUS’ comprehensive expertise can help you confidently interact with regulatory affairs authorities for different therapeutic area and package and present all the information necessary to allow regulatory authorities to make the right decision for passing registration pricess
  • 100% of approximately 140 submissions to the FDO have passed technical validation for registering IRC.
  • 50+ DIAF and 1.5 million pages published (all document types, e.g., DIAF /pharmacoeconomic/CTD ).
  • 70% of our regulatory professionals hold advanced degrees, with an average of more than 16 years of experience.