Medical device and IVD product registration in Russia

215.00

Medical device and IVD product registration in Russia

Description

Medical device and IVD product registration in Russia

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.