Medical Device Single Audit Program (MDSAP) for Manufacturers

GMED North America. is the subsidiary of GMED, leading Certification Organization & distinguished Notified Body (CE0459).GMED is a leading Certification Organization and a distinguished Notified Body (CE0459) whose scope covers all of the existing European Medical Device Directives (90/385/EEC, 93/42/EEC and 98/79/EC).GMED is also an Auditing Organization Recognized by the MDSAP Regulatory Authority Council and has been performing MDSAP audits since April 2015. GMED is accredited under the NF EN IEC/ISO 17021-1:2015 standard by COFRAC (Certificate № 4-0608), the French Accreditation Committee, to carry out Quality Management System Certification activities according to ISO 9001:2015 and ISO 13485:2016.Established in 1994, GMED is fully owned by LNE (e.1901), a State owned Industrial and Commercial Establishment (EPIC), and operates since August 1st, 2018 as a simplified joint stock company (SAS) within the LNE group.GMED’s success and high level of performance rely first and foremost on a strong and dedicated team of individuals trained at the highest level of the current evaluation and auditing methods to provide the best certification services: Certification Project Managers, Subject Matters Specialists (MDAO or Medical Device Animal Origin, Medicinal Substance, Active Implantable Medical Devices, Microbiologists), Technical Documentation Evaluators and Design Dossier Assessors, Clinical Reviewers & Experts (Ex: Sterilization Methods and Validation) and Auditors for CE marking and QMS activities.With offices in Europe and a dedicated US Operation created in 2005 - GMED North America (MD), GMED offers the convenience and efficiency of local teams of experimented specialists to accompany your certification process which will allow you to market in your target markets.

GMED North America, Inc.

Medical Device Single Audit Program (MDSAP) for Manufacturers; 2-Day Sessions; Online Training; March 30 -3`1, 2026.

Schedule (all times EST): 2-Day Session between 9:00am - 6:00pmAbout the trainingMDSAP should be considered as a strategic asset for organizations based globally, if they export or intend to export medical devices to participating countries.The program allows an MDSAP auditing organization to conduct a single regulatory audit of a medical device manufacturer that satisfies the relevant requirements of the regulatory authorities participating in the program.The program is beyond the pilot program and is now running full speed starting up to replace the normal structure audit.The countries which are using the MDSAP reports and certificates are Australia, Brazil, Canada, Japan, and the USA.Argentina’s National Administration of Drugs, Foods and Medical Devices (ANMAT) and Republic of Korea’s Ministry of Food and Drug Safety are now Affiliate Members and World Health Organization and European Union are Official Observers to the MDSAP Program. For program and more information, <a href="https://lne-gmed.com/training/transition-to-iso-134852016-mdsap-for-medical-device-manufacturers" title="https://lne-gmed.com/training/transition-to-iso-134852016-mdsap-for-medical-device-manufacturers" target="_blank" data-msys-clicktrack="0" rel="nofollow noopener noreferrer">click here.</a>

Medical Device Single Audit Program (MDSAP) for Manufacturers

More events from GMED North America, Inc.

Discover more events from GMED North America, Inc., from Business to other experiences you might love.

Still looking for the right event?

Explore all online events to browse and filter by date, category, and more.

Medical Device Single Audit Program (MDSAP) for Manufacturers

More events from GMED North America, Inc.

Discover more events from GMED North America, Inc., from Business to other experiences you might love.

You might also like...

Browse more events with different dates, prices, and formats to find your next great experience.

Still looking for the right event?

Explore all online events to browse and filter by date, category, and more.