Regulatory Support for Veterinary Clinical Trials

VetPharm offers a wide range of support services which facilitate the regulatory aspects of medical product development. These services include:

  • Regulatory strategy and plan development
  • Protocol development to meet regulatory requirements
  • Planning of, preparation for, and attendance at pre-development meetings and product approval conferences with CVM and other regulatory bodies
  • Pre-submission screening of study reports for consistency with agency expectations
  • Preparation and/or submission of INAD, NADA, and veterinary biologics license applications
  • Annual reports