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Medical Device Regulatory Compliance ConsultingRegulatory Affairs Consulting

Regulatory requirements impact your products – and your business – throughout their entire lifecycle. Especially when you consider that regulations are constantly changing. A single regulatory misstep or misunderstanding may stand between your financial success and misfortune. Our regulatory professionals work with you to develop and execute a roadmap to commercialization by ensuring you meet the evidentiary requirements that demonstrate the safety and efficacy of your medical device. Our experience covers regulatory requirements of the US, Canada and Europe.

Regulatory Affairs Consulting Services We Offer Include:

  • Regulatory Roadmaps
    • Strategy for US commercialization with FDA 510(k), PMA and de novo
    • Strategy for EU and Canadian commercialization with CE Marking
  • Regulatory Gap Analyses

SCHEDULE AN APPOINTMENT WITH ONE OF OUR REGULATORY AFFAIRS CONSULTANTS TODAY to ensure your device gets to market quickly and without unnecessary delay.