GTIMD can manage the complete pre-clinical, clinical, regulatory approval and post market process for your medical device. This service is provided for multiple approval pathways and regulatory bodies worldwide.

Services include:

  • Quality Assurance
  • Regulatory Affairs
  • Regulatory Strategy Development
  • Clinical Strategy Development
  • Pre-Clinical Study
  • Clinical Research trial management & monitoring
  • Data Management & Biostatistics
  • Submission Preparation Service