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Thursday, 20 June | Paris

MedTech Innovation Forum, France

Driving Innovation Through Effective Marketing and Clinical Collaboration

Register

Let's meet in Paris!

Date: Thursday, 20 June 2024
Time: 10:00 - 17:00 CEST
Location: Veeva Systems France

From ideation to launch, effective collaboration between clinical and marketing teams is essential to ensure product success.

Join your peers to discuss strategies and approaches to enable cross-team synergy, including:

  • Aligning clinical and marketing to optimize strategic evidence planning and claims for compliant product launches
  • Integrating  clinical insights into marketing strategies to optimize go-to-market
  • Streamlining processes for effective clinical evidence generation

The Forum is an excellent opportunity to network with peers in the France, learn, and share best practices.

Agenda:

  • 10:00 - 10:30 - Welcome and Introductions
    Get to know your peers in the region
  • 10:30 - 11:15 - Veeva Overview
    A quick overview of Veeva MedTech, and Vault Platform
  • 11:15 - 12:15 - Optimizing Strategic Evidence Planning
    Align clinical and marketing efforts for future competitiveness and significant contributions to specific clinical areas
  • 12:15 - 13:15 - Networking Lunch
  • 13:15 - 14:00 - Effective Clinical Evidence Generation
    Streamline clinical trial processes to ensure on-time data delivery for continuous product development
  • 14:00 - 14:30 - Break
  • 14:30 - 15:30 - Insight-driven Marketing
    Ensure the right clinical data for effective evidence and claims management
  • 15:30 - 15:45 - Closing
  • 16:00 - 17:30 - Networking Drinks
    Network and exchange ideas with your peers over tea and coffee
  • 18:00 - 20:00 - Dinner (Optional)
    Relaxed networking dinner

Complete your registration

Please complete the form below to reserve your seat.

Experts in the room

Rachel Mead

Rachel Mead

Clinical Regulatory Lead

BSI Group

Rachel Mead holds an Honours degree in Electronics and Electrical Engineering from the University of Glasgow and is a member of the Institution of Engineering and Technology. Rachel began her career twenty years ago as a research scientist in industry. Since then, she has held various research and development positions in medical device companies and has experience with clinical investigations of medical devices. Joining BSI as a Technical Specialist and Scheme Manager in 2018, Rachel currently holds the position of Clinical Regulatory Lead, where she has a particular focus on the clinical evaluation of medical devices.

Danielle Giroud

Danielle Giroud

Founder, CEO

MD-Clinical

With over 35 years of expertise in medical devices and diagnostics, Ms. Danielle Giroud founded MD-Clinicals, a specialized CRO based in Switzerland with offices in Frankfurt and Beijing. She's a renowned expert in clinical research and regulation, assisting global companies efficiently bring products to market. Additionally, as founder of the World Medical Device Organization, she provides extensive global training. Since 1998, she's played a pivotal role in ISO work and is currently the convener for ISO 14155 and 18969 on clinical evaluation. Ms. Giroud advocates for regulatory convergence, maintaining liaisons with entities like the EU Commission - Clinical Investigation and Evaluation task force and other global regulatory bodies.

Stepahnie Flipo

Stéphanie Flipo

Director of Clinical Strategy

MedTech EU

 

Ramona Galantonu

Ramona Galantonu

Director Commercial Strategy

MedTech EU

 

Pearl Vyas

Pearl Vyas

Director Strategy, Commercial Content

MedTech