Services By TypeRegulatory Certification
Regulatory certification is the process of confirming manufacturers’ compliance with regulatory requirements utilizing an audit and certification model, e.g. ISO/IEC 17021, to provide an inspectorate function on behalf of participating regulators. This function is differentiated from commercial certification which indicates conformance and registration for trade purposes by elevating it to regulatory compliance to meet legal obligations. Entities providing this function, the Auditing Organizations such as NSF Health Sciences Certification, LLC, have been assessed and formally recognized by participating regulators to perform this function on their behalf.
Latest News
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NSF Health Sciences Certification, LLC, Receives Authorization as Auditing Organization for MDSAP
- 10 months ago
ANN ARBOR, Mich. - NSF Health Sciences Certification, LLC, a wholly owned subsidiary of NSF International, was recently authorized as...
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NSF Health Sciences Certification, LLC Applies to Become MDSAP Auditing Organization
- 1 year ago
ANN ARBOR, Mich. — An application submitted by NSF Health Sciences Certification, LLC, a wholly-owned subsidiary of global public health...
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New CQI/IRCA-Certified Lead Auditor Training is First Based on ISO 13485 and International MDSAP
- 2 years ago
ANN ARBOR, Mich., USA and YORK, UK — NSF International, a global public health and safety organization, is now offering...
Upcoming Training & Education
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Quality Management Systems Lead Auditor Training, Incorporating ISO 13485:2016 and MDSAP Requirement
- Monday, March 11, 2019
- 8:30am - 12:00pm Eastern Time
- Reston, Virginia, United States
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Internal Auditor Training, Incorporating EU MDR and MDSAP Requirements
- Tuesday, March 26, 2019
- 9:00am - 5:00pm Eastern Time
- London, England, United Kingdom
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Internal Auditor Training, Incorporating EU MDR and MDSAP Requirements
- Tuesday, April 9, 2019
- 9:00am - 5:00pm Eastern Time
- Reston, Virginia, United States
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Quality Management Systems Lead Auditor Training, Incorporating ISO 13485:2016 and MDSAP Requirement
- Monday, May 13, 2019
- 8:30am - 12:00pm Eastern Time
- London, England, United Kingdom
Have questions? Need a quote? Want to get started? Contact NSF
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Info Paper: Benefits and Purpose of MDSAP
This paper provides an explanation on MDSAP and the benefits it offers to device manufacturers. Learn more
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Video: MDSAP Overview
Learn more about the MDSAP in this video featuring Kim Trautman, Executive VP, Medical Device International Services. Learn more
