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 achieving your business goals and an unwanted outcome.
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:
- Strategy for US commercialization with FDA 510(k), PMA and de novo
- Strategy for EU market entry with CE Marking
- Strategy for Canadian commercialization
- Strategy for entering other global markets
Regulatory Strategies & Compliance Initiatives
- GxPs, 21 CFR Part 11 and Annex 11
- European Directives and CE Marking
- FDA Submissions to Obtain FDA Clearance
- Medical Device Technology and Software Validation
- Human Factors Validation
- Representation before Regulatory Bodies
- Document Preparation
- Guidance for Pre-Submission Meetings
- Risk Assessment and Remediation Strategies
- Submission Changes
Quality and Product Certifications
- IEC 60601-1 3rd Edition Amendment 1 Safety Testing Documentation Preparation
- ISO 14971: 2012 Compliance and Documentation Preparation
- IEC 62304 Software Development Lifecycle Compliance
- ISO 13485 Compliance and Documentation Preparation
- Test Laboratory Document Submission
- 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
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!