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Almost every aspect of medical devices is covered by regulations, rules and standards, so very few actions are possible without being aware of the appropriate regulation, rule or standard. This is equally true whether you are seeking an approval for a medical device, undertaking a clinical investigation, reporting an adverse incident or seeking government reimbursement. Successful medical device manufacturers need well-trained regulatory, marketing, quality and engineering professionals with the knowledge of the appropriate market or standard.

SGS has entered into a strategic partnership with World Medical Device Organisation (WMDO) to bring a program of 200+ e-learning courses to your professional environment. The medical device industry’s most trusted source for professional online training consists of an unparalleled range of courses suitable for regulatory affairs, quality, marketing, and commercial, clinical, manufacturing and design staff of organisations varying in size from one to beyond 10,000 people. Courses cover the regulatory requirements of many global markets from EU and US to Brazil and Singapore, clinical evaluation and investigations, risk management, quality systems and healthcare economics. They are all devised to introduce the basic information vital to your organisation’s success and can match the training requirements of individuals or groups and offer larger organisations management tools for monitoring learning progress. These e-learning solutions complement the existing public classroom courses the tailored in-house learning and development programs provided by SGS ACADEMY.

For more information and to continue to develop the talent within your organisation please go to the WMDO Website or contact the Medical Devices Team.