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Risk management is a complex but necessary process for medical device companies, and its complexity has only heightened with the introduction of more stringent regulatory requirements under ISO 14971 and the Medical Device Regulation (MDR). It is crucial to learn how to correctly modify your approach, so that you are harmonised with the new Regulations and can guarantee your compliance.
This online course will provide you with a complete overview of the key regulatory considerations for risk accompanied by the tools and techniques you can use to implement them, for both professionals new to the area and those who need an update on the latest developments. You will be able to cement this knowledge through an entire module on case studies based off the trainer’s own experiences, so you can practically apply the information you have learned.
Suitability - Who should attend?
This course will be useful for personnel involved in risk assessment and risk management activities, and for those who are new to the industry and need a complete overview of the medical device regulatory framework in the EU. It will be applicable for professionals in:
- Regulatory affairs
- Quality assurance
- Product managers
- Design engineers
- Clinical staff
- Project managers
Training Course Content
- Understand the importance of ISO 14971 and how to apply it to your own processes
- Identify links between ISO 14971 and ISO 13485
- Improve your understanding of the risk requirements under the MDR and distinguish its differences from the MDD
- Develop your skills in risk management planning by learning about key methods for project management
PTI - Pharmaceutical Training International - Training for the Pharma Industry
PTI is the global leader in professional education for the pharmaceutical industry, delivering a broad course portfolio that covers the industry spectrum: R&D, Clinical Development, Generics, Bio-pharmaceuticals, fine Chemicals, Agro-chemicals, Medical Devices, Animal Health, Manufacturing and Regulations. PTI's open courses,...
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