MDSAP is a single audit program that consists of one single regulatory audit of medical device quality management systems to meet relevant requirements of multiple regulatory authorities. Established by the International Medical Device Regulators Forum (IMDRF), the MDSAP supports a global auditing and monitoring approach for medical device manufacturing to assess the compliance of products used in the medical field.
As an authorized auditing organization, we offer the full range of necessary MDSAP audit services to assess if manufacturers meet the quality and regulatory criteria required by market regulators as well as the expectations of medical professionals and those under their care.
Our expert auditors perform efficient and effective assessments to provide you with the opportunity to gain the certification you need to satisfy the requirements of the following international regulatory authorities:
Contact us for more information about our MDSAP services!
Our comprehensive MDSAP auditing and certification services can give you a significant reduction in overall audit time needed to demonstrate compliance with multiple regulatory requirements through a single audit program. Many regulatory authorities may accept MDSAP results as an alternative to their own inspections when processing applications for medical device marketing authorization. Our program also combines the requirements of CE approvals with MDSAP thus further making compliance auditing as efficient as possible Reduce your corporate risk and protect your business with our recognized MDSAP audit and certification.
MDSAP has been put into place to develop, manage and oversee an independent audit program in which manufacturers of medical devices can present the results of a single regulatory audit to prove compliance and qualify for market entry in multiple countries and jurisdictions. MDSAP inspection of a manufacturer quality management system (QMS) must be conducted by an authorized auditing organization (AO). Our worldwide auditing resource is qualified under the MDSAP program
Our comprehensive MDSAP auditing services for medical device quality management systems follow a three-step audit cycle:
Initial certification audit - Stage 1
Review of key documentation, readiness and planning
Initial certification audit - Stage 2
Evaluate QMS compliance to ISO 13485 and all MDSAP regulation. Once the initial certification audit has been successfully completed, the MDSAP certificate will be issued, which will be valid for three years.
Annual audit to assess ongoing compliance, effectiveness of changes in products or QMS processes
Every three years to determine manufacturer QMS suitability, effectiveness and compliance to MDSAP requirements
Manufacturers must be audited according to the scope declared in their applications for certification. Our experts determine which regulatory requirements apply to each manufacturer based on the countries in which medical device products are registered, sold or planned to be sold.
Applicable norms and standards:
We provide comprehensive MDSAP services for manufacturers in the medical device industry. We are a Notified Body and Quality System Certification Body as well as an accredited testing house. Our service portfolio includes QMS auditing for suppliers and sales offices and comprehensive device testing services via our worldwide network of engineers and laboratory facilities. We can help you navigate complex market requirements with support in specific national testing needs and registration procedures. We are your innovative and ready partner for future digitalization applications in areas such as wireless, telemedicine and medical apps as well as cyber security - NL and personal data protection.
Learn how you can benefit from MDSAP auditing!
Receive more information about our MDSAP services by reading our FAQ, which answers the following questions:
|FAQ – MDSAP||260 KB||Download|