Sponsored:Literature review optimisation for medical devices

Sponsored:Literature review optimisation for medical devices
FREE SPONSORED WEBINAR - This webinar will describe the current state of RWE scientific advancements and provide context for the regulatory and research implications of RWD and RWE.

24 November - 15:00 -16:00 GMT / 16:00 – 17:00 CET

How to optimize the literature review for medical devices to ensure EU MDR compliance 

Navigating the European Union Medical Device Regulation (EU MDR) requires a thorough understanding of the literature review process. In this informative webinar, after an overview of the EU MDR and its impact current organization, we will guide you through the key steps to optimize your literature review, ensuring compliance with EU MDR requirements.

Target audience:
- Regulatory Affairs & Safety Professionals
- Clinical Research & development Teams
- Quality Assurance & Quality Control Professionals
- Consultants & Auditors
- Academics & Researchers
- Anyone interested in EU MDR Compliance

Learning outcomes:
- Comprehend the role of literature review in compliance,
- Acquire practical insights and best practices for optimizing the literature review process from 
data source selection to data integrity,
- Receive information on valuable resources, tools & further educational opportunities

Speaker:

Nicole Baker, CEO, Biologit

Nicole is an Immunologist and Pharmacovigilance Professional with strong focus on innovation and extensive knowledge in global legislation and guidelines for Medical Affairs, Regulatory Affairs, Pharmacovigilance and Clinical Trials, gained by leading and managing global, multi-disciplinary teams.

Extensive experience in providing strategic, operational and scientific leadership throughout the product life-cycle, from pre-clinical to post-marketing. In addition, experience gained supporting or fulfilling the role of EEA QPPV and RPPV in Clinical Trials over the last decade and over 25 years’ experience gained within Academia, Pharmaceutical Industry, Regulatory Authority, Clinical Research Organisation, and more recently Start-up.
 
This webinar is sponsored by Biologit 



Disclaimer: Whilst TOPRA is running this webinar for Biologit, this is not an endorsement of Biologit, Biologit's affiliates, employees or its products and services. TOPRA is also not responsible for the content or views expressed during the webinar.

How do I register?

Simply log in or create an account and register below.

Pricing

  • Members: free
  • Non-members: free

Terms and Conditions

By purchasing this webinar, you are agreeing to TOPRA's training terms and conditions.

 

 
When
24/11/2023 15:00 - 16:00
Where
ONLINE
Registration is closed
My registration status: Not registered
Your company name
Your VAT country
Your VAT number
NOTE
Important instructions before booking - If your company name or VAT number does not appear here or you would like to be invoiced using a different VAT number, please email finance@topra.org

Register now