| MEDICAL DEVICES AND APPLICABLE REGULATIONS
Availability: Right Now (Recorded Presentation) Duration: 70 min. (the average time to complete the training program). |
Description:Â This webinar course will take you into the Medical Device Regulation field providing guideline, giving example and references to the applicable laws and standard. Â An overview of discussed topic is here reported:
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| 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:
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: Alice Ravizza is a Biomedical Engineer, graduated at Politecnico di Torino. 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. |
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Cooperation Opportunities for SME
Free Regulatory Resources
Here you can find a free and organic collection of Regulatory and Quality guidelines.
