Medpass International

Medpass International

  • 9600 W 76th St Ste T
  • Eden Prairie, Minnesota
  • 55344-3922

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Description

With over 20 years of experience , we have an unparalleled mix of regulatory, clinical and reimbursement expertise that is leveraged to provide clients with efficient and cost-effective roadmaps to market.

MedPass’ clients range from global medical device manufacturers to start-ups. Our reimbursement work leverages on our extensive experience backed by strong working relationships with Government Authorities, Healthcare Institutions, HTA Bodies and Notified Bodies across Europe.

She was subsequently promoted to senior assistant in the Regulatory Affairs department with responsibility for Authorised Representative services and our Adverse Event Surveillance Unit. Julie has extensive experience of the medical device industry and the essential requirements for successful trial outcomes.

Jeremy Tinkler has extensive experience of the whole range of regulatory activities associated with medical devices, gained from 20 years with the Medical Device Sector of the UK Medicines and Healthcare products Regulatory Agency (MHRA). Jeremy, who is a toxicologist by training, held the position of Principal Specialist, Biosciences and Implants at MHRA and was responsible for the technical direction of safety assessments and adverse incident investigation activities for a wide range of devices.

We are the “one stop shop” for medical device manufacturers seeking access to the European market.

Products & services

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