Free Regulatory Consultation For Your Medical Device

Learn actions needed to pass US, Canada and EU Regulations

Review your device plans 

Determine Regulatory Approval steps required 

Our team of medical device regulatory professionals will review your medical device and activities, then provide you recommendations drawing upon 15 years experience with over 100 medical devices.

Gather specific feedback on:

  • US, EU, and Canadian requirements for your medical device
  • Expected timelines and costs
  • Potential hurdles or issues specific to your device
  • Implementation Options and Resources

Vesna Janic, Director QA/RA

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