The "Navigating through Maze of In-vitro Diagnostics (IVD) Regulations: A systematic approach from Regulatory Strategy to Regulatory Approvals in U.S./Europe/Canada" conference has been added to ResearchAndMarkets.com's offering.
In-vitro Diagnostics (IVD) products provide critical information on a patient's health condition, based on which the healthcare provider develops and administers treatment plans. Although IVDs are medical devices, they are regulated under a separate set of regulations in the U.S., Europe, and Canada.
This 2-day interactive course on in-vitro diagnostics is structured to understand the different sets of IVD regulations, how to navigate through this maze of IVD regulations, and to win regulatory approvals. This In-vitro Diagnostics (IVD ) course will make the attendees understand the IVD regulations and develop regulatory strategies that secure regulatory approvals.
After completion of this two-day interactive course on IVD, the attendee will be able to:
Understand why IVD is regulated differently.
An overview of IVD Regulations - U.S. FDA., Europe (MDD), Canada.
Develop Regulatory Strategies and determine Regulatory Pathways.
Inclusion and exclusion of data and information for different submissions.
Format and Content of premarket submissions.
Product Label and Labeling for IVDs.
Working and interacting with the reviewers and regulators.
Tips and Suggestions to secure rapid regulatory approvals.
Who Should Attend:
This interactive course is specifically developed for individuals, who are responsible for the design, development, manufacturing, marketing, and distribution of IVD products.
This course is highly recommended for personnel involved in any of the following functions:
Department Managers (middle management)
Research & Development (R&D)
Product Design & Development
Day 01 (11:00 AM - 6:00 PM EST)
Evolving technologies and challenges of In-vitro Diagnostics (IVD) products
Why the regulators need separate regulations even IVD is considered a device?
Know the process and players at OIR (aka OIVD) of CDRH and Health Canada
Overview of US-FDA Regulations for IVDs
Determination of classification & Identification of Predicate Device(s)
Development of Regulatory Strategies and Pathways for IVDs
Special consideration of IVD labeling requirements
Determine the type of the required pre-market submission for your IVD
Format and Content of 510(k), Pre-IDE, IDE, and PMA
What is a Clinical Laboratory Improvement Amendment (CLIA) of 1988?
Preparation and submission for CLIA Waiver Application
Day 02 (11:00 AM - 6:00 PM EST)
Overview of European IVD Regulations
Understanding of EU MDD 98/79/EC for IVD and applicable MEDDEV documents
Special consideration to Classification Rules for IVDs
Conformity Assessment for CE Marking
Special Labeling and electronic Labeling Requirements for IVDs
Preparation of Technical File or Design Dossier
Overview of Canadian Medical Device Regulations (CMDR) for IVDs
Understanding similarities and differences between U.S. and European regulations
Format and Content of Canadian Medical Device License (MDL) Application
Inclusion of the required data and information for MDL application
Conclusion & Summary of the course
For more information about this conference visit https://www.researchandmarkets.com/r/hmgem6
View source version on businesswire.com: https://www.businesswire.com/news/home/20210301005776/en/
Laura Wood, Senior Press Manager
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