DURATION:

50 min + 10 min. Question Time

Description:

Prerequisite: basic knowledge of medical devices

Contents:

-Basic registration analysis,

-Legislation framework,

-Classification rules,

-Registration process depending on risk class,

-Documents from manufacturer side,

-Basic understanding of pre-clinical,

-Best clinical trials strategy,

-Declaration issues.

Who Will Benefit:

• Quality Manager
• Quality Engineers
• Design Quality
• Regulatory Affairs specialist
• Medical Affairs specialist
• Clinical Affair specialist
• R&D 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:

• Answer to questions submitted during the webinar.
• An online final assessment with multiple choice questions.
• A Certificate of Completion.