Quality Managers and Coordinators
Those responsible for the QMS at medical device manufacturers, importers and distributors.
A 24-hour programme training Internal Auditors for medical device Quality Management Systems, integrating ISO 13485:2016, ANVISA RDC 665/2022, the new ISO 19011:2026 guidelines (4th edition) and ISO 14971:2019/Amd 1:2020 risk management.
12 technical distinctions that no national or international competitor covers in full.
Comprehensive training in medical device QMS internal auditing, from ISO 13485 clauses to a practical audit simulation.
8 professional profiles that benefit directly from the programme.
Those responsible for the QMS at medical device manufacturers, importers and distributors.
Professionals who conduct or intend to conduct first-party and second-party QMS audits.
Those involved in regulatory compliance, ANVISA registrations, CE marking and certification.
Those responsible for implementing and overseeing the QMS under ISO 13485.
Those involved in the design, development, validation and control of medical devices.
Specialists in quality, regulatory affairs and medical devices.
Professionals marketing medical devices and healthcare products in Brazil.
Pharmacists, engineers and other professionals appointed as the responsible technical professional (RT) with ANVISA.
24 hours of intensive training, content unique to the Brazilian market and an HSC Global certificate on completion. Speak to our team to reserve your place.
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