Wability’s regulatory affairs group is skilled in navigating the long process of obtaining a product registration. Our knowledgeable team works with our clients to prepare and complete global or local submissions, and interacts with regulatory agencies to expedite successful authorization. Our regulatory affairs services include:

  • Regulatory Strategies
  • NDA and Pharmaceutical Documentation
  • Clinical documents (including ISS and ISE)
  • Expert reports and summaries
  • Submission through authorization
  • Regulatory consultancy for most regulatory issues
  • Investigational drug brochures
  • Clinical trial applications (CTX/IND)
  • Clinical study reports, manuscripts, PSUR
  • GCP Compliance