Nature :
Diploma (bac+5 level)Titled :
Professional Master: Regulatory Affairs of Medical DevicesContact - Name & First name:
Dr Imane DAKKA - Asst. Prof. Jean Marie OUEDRAOGO - Prof S. AHIDContact - Email:
j.ouedraogo@ueuromed.org / contactpharmacie@ueuromed.orgContact - Telephone:
00212616495062Training aims
Presentation :
This master's degree offers comprehensive training covering the scientific, clinical, regulatory and industrial aspects related to medical devices. It thus allows participants to master all areas essential to the design, development, marketing, and management of medical devices in an increasingly demanding environment.
Goals :
The medical device is an essential health product, intended for human use, for diagnostic, therapeutic or metabolic purposes. It encompasses a wide range of applications, from simple products such as needles or compresses, to sophisticated equipment such as scanners or pacemakers. Faced with growing global demand and in a context of intense competition, the medical devices sector is characterized by constant innovation in research and development. To guarantee patient safety and effectiveness, the regulations surrounding these products are constantly evolving to adapt to new requirements.
This 1-year master's degree aims to provide participants with in-depth skills in several key areas, including:
- The regulation of medical devices in Morocco and Europe,
- The integration of new technologies and sustainable development in medical devices,
- Communication and marketing specific to medical devices,
- Quality management and control of risks associated with medical devices,
- Entrepreneurship in this growing sector.
Admission:
Training(s) required
- Professionals in the field of medical devices,
- Diploma of Doctor of Pharmacy
- Diploma of Doctor of Medicine
- Diploma of Doctor of Dentistry
- Biomedical General Engineering Diploma
- Veterinary Doctor Diploma
- Students in Pharmacy, Medicine, Dentistry
- Students in scientific branches
- Students at the end of their pharmacy course
Program
- Development and research process
- Specificity of MD: classification rule
- Place of medical devices in therapy
- Regulation of MDs in Morocco
- EU MD Regulation (MDR)
- MD quality management (ISO 13485)
- Risk Management linked to the use of DM
- Clinical evaluation of MDs (Moroccan and European context)
- Access to the Market and reimbursement; DM economies in Morocco
- Materiovigilance and traceability
- Marketing and communication of medical devices
- Medical device technologies
- Sterilization of medical devices and biocompatibility
- Environment and Sustainable Development of medical devices
- DM Entrepreneurship
The program combines lectures, case studies, bibliographic monitoring, as well as group work organized every other weekend, culminating in a final written exam.
The training also includes the oral defense of a tutored project thesis, presented before a mixed jury composed of teachers and professionals.
Target audience:
- Pharmacists, doctors, biomedical engineers, professionals in the field of medical devices, students in scientific branches
- Students at the end of their pharmacy, medicine or dentistry courses
Prerequisites:
- Doctorate in pharmacy, medicine, dentistry, biomedical engineering diploma or equivalent
- Bachelor's degree in biology, biomaterials and health sciences or equivalent
Registration :
Complete the registration form and send it to Professor Jean Marie OUEDRAOGO
Email:
j.ouedraogo@ueuromed.org/ contactpharmacie@ueuromed.org
Tel: 00212616495062
Home establishment: Euromed Faculty of Pharmacy – UEMF
Last registration deadline:
- November 15, 2024
Limited places.
Place :
Casablanca for residents in Morocco and Remote for residents outside Morocco.