Doctor researching medicine

With 25+ years in pharmaceutical development, Innovenn has deep knowledge of the sector and its regulations.

We’ve worked with numerous disciplines associated with the path to marketing approvals for chronic and rare disease management – from filing Investigational New Drug Applications (INDs), to enacting clinical programs continuing on through New Drug Application (NDA) submission.

Our integrated strategic planning services enable our partners to deliver new tools that are intended to support patients, enable precision medicine, improve outcomes and accelerate relevant scientific advances.

Clinical Studies and Validation Services for Drug, Devices, SaMD, and Digital Therapeutics

  • Site Management and Monitoring
  • Medical Monitoring
  • Safety and Risk Assessments
  • Compliance GCP, CLP, GMP
  • Regulatory and Quality Oversight
  • Institutional Review Board (IRB) Management
  • Participant Recruiting
  • Data Management
  • Device Shipping and Supplies
  • Statistics
  • Medical and Technical Writing