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Regulatory 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 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 regulatory affairs consulting meets global regulatory requirements, including 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

Regulatory Compliance Initiatives

FDA Submission Support

  • Document Preparation
  • Guidance for Pre-Submission Meetings
  • Risk Assessment and Remediation Strategies
  • Submission Changes

Quality and Product Certifications

FDA Auditing Services

  • Internal Audits and Compliance Remediation
  • External Audits and Vendor Management Compliance

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

Get in Touch with a Regulatory Affairs Consultant

Talk to a Regulatory Affairs Consultant

Interested In Our Regulatory Affairs Consulting Services?

If you’d like to learn more about how the MethodSense team can support your commercialization and compliance goals, drop us a line. We look forward to speaking with you!