Mon, Jun 22 · 8:25

Join 700+ medical device, IVD and combination product professionals on 22-26 June 2020 in Dublin to get the latest regulatory insights and practical advice for implementing the EU MDR, IVDR and Global Market regulations.

Get the latest regulatory guidance direct from 20+ Competent Authority and Notified Body representatives to gain clarification on the requirements and their expectations. And, benchmark your regulatory progress with leading industry case studies including strategic advice to help ensure you're on track for compliance.

Get all of your updates under one roof with the opportunity to move between all of the conference tracks on the days you choose to attend:
- EU Medical Device Regulation - 22-23 June 2020
- EU Medical Device Law - 22-23 June 2020
- Post Market Surveillance And Vigilance - 23-24 June 2020
- Clinical Evaluations And Investigations - 23-24 June 2020
- TRAINING COURSE: Medical Device Regulatory Project Management - 24 June 2020
- TRAINING COURSE: US Regulatory Affairs for Medical Devices - 24 June 2020
- Medical Device Regulatory Affairs in Global Markets - 24-26 June 2020
- Software and AI - 25 June 2020
- TRAINING COURSE: Medical Device Clinical Data Management - 25 June 2020
- EU IVD Regulation And Strategy - 25-26 June 2020
- Drug Device Combination Products - 25-26 June 2020
- Sterilisation And Reprocessing of Medical Devices - 26 June 2020

Build your 2, 3, 4 or 5 day pass and secure your place today. You will gain full access to all conference tracks and training courses on the days you choose to attend so be sure to take a look at the full 5 day agenda.

For sponsorship and exhibition opportunities, please get in touch.

URLs:
Sponsor: https://go.evvnt.com/601480-3?pid=5731
Twitter: https://go.evvnt.com/601480-4?pid=5731
LinkedIn: https://go.evvnt.com/601480-5?pid=5731

Prices:
2 Day Pass: GBP 1999.0,
3 Day Pass: GBP 2599.0,
4 Day Pass: GBP 3099.0,
5 Day Pass: GBP 3399.0

Speakers: Gavia Taan, Unit Manager - Devices Regulatory Policy Devices Division, MHRA, Thomas Wejs Moller, Section Manager - Medical Devices, Danish Medicines Agency, Augusto Geyer, Deputy General Manager, Medical Devices Office, ANVISA, Brazil, Sasikala Devi Thangavelu, Director, Policy, Code And Standard Division, Medical Device Authority, Ministry of Health, Malaysia, Elaine Darcy, European Medical Device Operations Manager, NSAI, Daniele Bollati, Product Conformity Assessment /Medical Devices Expert, IMQ, Pedro H A Eerdmans, Global Director Clinical, Dekra Certification BV, Andreas Stange, Vice President MHS global IVD, TUV SUD, Inge Vandenbussche, Director Regulatory Affairs EMEA, Medtronic, Erik Vollebregt, Partner, Axon Lawyers, The Netherlands, Ela Bingel-Erlenmeyer, Deputy Director of Clinical Affairs, Geistlich, Maham Ansari, Director of Regulatory Affairs, Synaptive Medical, Canada

Venue Name: Citywest Hotel