An NSF International Company NSF Health Sciences’s Medical Device Diploma
In collaboration with Sheffield Hallam University
- About QP Training
- QP Training Modules
- Post Graduate Certificate and Diploma
- Useful Links And Downloads
What is a Qualified Person?
The European commission recently issued proposed legislation for manufacturers in the medical device industry to have a medical device “Qualified Person” (QP) in regulatory affairs and quality assurance.
The person specification in the proposed legislation parallels a similar requirement in the Pharmaceutical industry, and certain medical device regulations under German law.
Based on this information, NSF Health Sciences and Sheffield Hallam University have collaborated to produce a pathway to becoming a medical device Qualified Person. The programme consists of three steps, the Postgraduate Certificate, Postgraduate Diploma and gaining a medical device Qualified Person status with or without an MSc.
NSF Health Sciences offers a series of professional training courses to address the demands for a medical device Qualified Person responsible for the most critical phases of your Product Lifecycle
Our Medical Device QP Programme
Do you play a role in quality management and regulatory affairs? Is success achieved on a day-to-day basis because of your knowledge and skills in medical device regulatory affairs and quality assurance?
Ensure your abilities are recognised by attending NSF Health Science’s Qualified Person Programme for medical devices and achieve accredited competency requirements.
NSF’s Medical Device Qualified Person Programme addresses the needs of the medical device industry with a range of postgraduate qualifications.
Your Success
- Avoid the disruption of attending courses that do not address your specific technology, market or problem
- Learning is applied immediately and subjected to competency assessment by industry experts
- Learning is blended into your work-based projects
- Customize your learning by introducing in-house programmes.
Why NSF Health Sciences?
NSF Health Sciences has 25+ years of experience delivering university-accredited training to the medical device and pharmaceutical industry. We have a deep knowledge and a wealth of extensive experience in the challenges and solutions faced by medical device professionals on a day-to-day basis. Our professional medical device courses are designed to address these challenges by offering practical solutions and support to the modern day Quality and Regulatory professional.
NSF is the perfect training provider to meet your needs.
Eight Reasons Why You Should Choose NSF Health Sciences
NSF’s collaboration with Sheffield Hallam University has brought about a highly challenging but rewarding professional training course in the form of medical device qualified persons (QP) diploma for all medical device professionals
1. Utilise your prior learning - No need to re-attend training
2. Gain quality professional status - NSF’s affiliation with various professional and academic institutions ensures your skills are recognised
3. University accredited - NSF is the only training provider to offer flexible, accredited postgraduate qualifications to the medical device industry in Quality Assurance & Regulatory Affairs
4. Practical learning from the best - “Learning through doing with experts at your side”
5. Supported learning - Communicate with NSF’s carefully selected trainers about any current issues you are facing or support on your qualification.
6. Flexible learning - Work around your existing commercial and personal commitments. Pick and choose when to study and for how long; either at our facilities or in your own company with courses that are tailor made for you.
7. Modular - A modular structure allows you to focus on important and relevant subjects to you enabling you to optimise your study-work-life balance
8. Extensive experience - NSF has 25+ years’ experience (formerly David Begg Associates) in training professionals from the healthcare industries at postgraduate level. Our team of experts regularly work with both regulatory agencies and industry leaders.
