Have you been left in a muddle surrounding the new ISO14971:2012? Have you faced such questions as:
Join this training course to gain an insight into risk management and answers to these questions.
Risk management is a fundamental step for medical device manufacturers to demonstrate compliance to the EU Medical Device Regulations, ensuring the safety of patients and users. Since the introduction of the ISO14971:2012, there has been a lot of confusion surrounding the implementation of the new standards, by medical device manufacturers.
This course will be delivered by Acclaim Biomedical Consulting, with over 20 years experience in Medical Devices, they are best placed to support and advise on the regulatory changes and the impact these will have on existing practice.
This full day course will cover:
This training course is aimed at leading Risk Management Teams, Quality Regulators and Senior Managers.
For more information, please email Vanessa Bailey on VanessaB@medilinkwm.co.uk.