MEDICAL DEVICES AND APPLICABLE REGULATIONS Download the Course BrochureAvailability: Right Now (Recorded Presentation)Duration: 70 min. (the average time to complete the training program).
Description: This webinar course will take you into the Medical Device Regulation field providing guideline, giving example and references to the applicable laws and standard. An overview of discussed topic is here reported:
Manufacturer definition, obbligations and responsability
Device classification and CE Mark path
Why Should You Attend:
Continuing education and professional development are critical to the regulatory professional. Regulatory professionals must keep up to date with regulatory policies and procedures for one or more countries, as well as maintain an understanding of the scientific and technical background of healthcare products. A clear understanding of regulatory process and applicable regulation is necessary for creating technical documentation, maintain up to date existing one and assure compliance. This webinar course will provide a comprehensive overview and guidance to the Medical Device regulation.Who Will Benefit:
Regulatory Affairs specialist
Medical Affairs specialist
Clinical Affair specialist
R&D Engineers
Quality Engineers
Marketing
Certification Requirements: Students must view the entire program and successfully pass an online, multiple choice final assessment with >80% passing grade.Certificate will be printable in PDF format immediately after satisfying requirements.
Online Training Programs Includes:
90 days of 24/7 access to individual eLearning courses.
Answer to questions submitted during the webinar.
An online final assessment with multiple choice questions.
A Certificate of Completion.
Course Presented and Commented by:
Alice Ravizza is a Biomedical Engineer, graduated at Politecnico di Milano. She has great and extensive experience in R&D and QA / RA in the biomedical field. She is specialized in supporting Medical Device companies in building up and improve Quality System Management and assure Compliance through all the internal processs. She assist companies during the registration process for CE Mark making sure all the technical documentation is compliant to applicable standards and regulations. She is aswell an experienced Trainer and Lecturer.
Medical Devices and applicable Regulations – Commented Interactive Presentation Webinar
€195.00€135.00This course provides a comprehensive introduction to the Medical Devices Regulation.
Descrizione
Download the Course BrochureAvailability: Right Now (Recorded Presentation)Duration: 70 min. (the average time to complete the training program).
Continuing education and professional development are critical to the regulatory professional. Regulatory professionals must keep up to date with regulatory policies and procedures for one or more countries, as well as maintain an understanding of the scientific and technical background of healthcare products. A clear understanding of regulatory process and applicable regulation is necessary for creating technical documentation, maintain up to date existing one and assure compliance. This webinar course will provide a comprehensive overview and guidance to the Medical Device regulation.Who Will Benefit:
Certification Requirements: Students must view the entire program and successfully pass an online, multiple choice final assessment with >80% passing grade.Certificate will be printable in PDF format immediately after satisfying requirements.
Online Training Programs Includes:
Course Presented and Commented by:
Check Free Resources – Major European Regulations
[supsystic-social-sharing id=’1′]
Prodotti correlati
Corso Webinar Sterilizzazione Dispositivi Medici: ETO, GAMMA, STEAM, Shelf Life, Validazione
€275.00€195.00 Aggiungi al carrelloWEBINAR FDA REGISTRATION: MEDICAL DEVICE, IVD, COMBINATION DEVICE [ENG]
€45.00 Aggiungi al carrelloCorso Webinar – Traditional 510(k) – FDA Registration – US Medical Device Regulatory + 510(k) Ready Template [ENG]
€199.00€119.00 Aggiungi al carrelloCorso WEBINAR – ISO 13485:2016 MEDICAL DEVICE QMS TRANSITION TRAINING – RECORDED WEBINAR [ENG]
€255.00€165.00 Aggiungi al carrello