Join 500+ medical device, diagnostics and combination product experts in Brussels on 17-21 June 2019 to hear about the latest updates, insights and implementation strategies surrounding the EU MDR, IVDR and Emerging Market regulations. Plus, put your questions to 15+ Competent Authority and Notified Body representatives and benchmark with industry case studies to ensure you're on track for compliance.
Get all of your regulatory updates under one roof across 5 days with 9 streams of expert guidance and 2 training courses:- EU Medical Device Regulation (17-18 June 2019)- EU Medical Device Law (17-18 June 2019)- Clinical Evaluations and Investigations (18-19 June 2019) - Post Market Surveillance and Vigilance (18-19 June 2019)- TRAINING COURSE: Medical Device Regulatory Project Management (19 June 2019) *NEW*- Medical Device Regulatory Affairs in Emerging Markets (19-21 June 2019)- Clinical Outsourcing (20 June 2019) *NEW*- TRAINING COURSE: US Regulatory Affairs for Medical Devices (20 June 2019) *NEW*- EU IVD Regulation and Strategy (20-21 June 2019)- Drug Device Combination Products (20-21 June 2019)- Sterilisation and Reprocessing of Medical Devices (21 June 2019)
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 make sure you take a look at the full 5 day agenda.
2 Day Pass: GBP 1899.0
3 Day Pass: GBP 2499.0
4 Day Pass: GBP 2799.0
5 Day Pass: GBP 3199.0
Time: 9:00 am - 5:00 pmmore
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