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22-23 June 2017
Hotel Okura,
Amsterdam

Achieve the fastest regulatory pathway for combination product classification and approval through Competent Authority feedback and industry case studies

Thank you to everyone who attended this year's Drug Device Combination Products

Thank you for another successful year at Drug Device Combination Products


We would like to extend a very big thank you to everyone who attended this year's Drug Device Combination Products. The event delivered the latest updates on the European Medical Device Regulations and the implications for combination products; provided vital insight direct from the 3 key stakeholders: Competent Authority, Notified Body, and industry; and brought the combination product community together for stimulating discussion, ample networking and industry benchmarking. It was great seeing so many familiar faces, as well as meeting lots of new ones. 

Mark your calendar - The dates for our 2017 meeting have been released and we are pleased to announce that next year, Drug Device Combination Products will be taking place along side 6 other events as part of the MedTech Summit in Amsterdam at the Hotel Okura on 22-23 June 2017. We look forward to seeing you there!

2016 Sponsor & Exhibitor Testimonials:

“Good event to contact and network with the right people in this business” - Toxikon

"Very well organized. Linda and Lidia were especially helpful in coordinating our sponsorship and increasing the visibility of our company" - GLR Laboratories Pvt Ltd

Bringing together 8 Competent Authority and Notified Body speakers and...

70+
Combination Product Professionals
50+
Medical Device and Pharmaceutical Companies
8+
Networking Hours

Meet, benchmark, and be inspired by the industry's leading experts

Who Can You Expect to Meet?

Senior Director/Director/Head of/Manager/Associate

  • Regulatory Affairs
  • Product Development
  • Drug Delivery
  • Quality/QA
  • Combination Products
  • Compliance
Additional Learning Opportunities

Pre-Conference Focus Day

Essential Key Updates on the European Medical Device Regulations

Click here for details on this session

Post-Conference Workshop

The New EU IVD Regulation and Companion Diagnostics

Click here for details on this session

Enhanced Networking

Evening Drinks Reception

  • Grab a drink and join your peers for an evening of socialising.

2 Conferences in 1 Location

  • The meeting will be co-located with our Biocompatibility for Medical Devices conference, providing enhanced networking opportunities and a platform for cross-functional discussion.

2016 Promotional Participant

In association with for 2016

Medical Device Training International | MDTI


MDTI is a global interactive training partner committed to the personal progression of Medtech professionals. We deliver CPD certified training on a wide range of topics including clinical evaluations, clinical investigations, regulatory affairs, combination products, PMS and vigilance, In Vitro Diagnostics (IVD)and soft skills. Our courses are delivered in a variety of formats such as public face-to-face, customised in-house, webinars, eBooks and online academies.