EU Medical Device Post-Market Clinical Evaluation Planning Conference

October 29-30, 2019 | Frankfurt, Germany

Le Meridien Frankfurt Hotel

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Special Thanks to Our Sponsors



RQMIS, located in the US, UK and EU, is a solutions-driven provider of therapeutically focused, comprehensive regulatory consultation to the global medical product industry focused in several areas including clinical study design/management.

RQMIS has successfully collected, queried, analyzed and published results from 3 clinical sites in Germany within a 6-month window for an Artificial Spinal Disc PMCF. Currently, RQMIS is managing additional PMCF studies, one study supports CE marking and will be submitted through the FDA for consideration of a change in intended use. Both are expected to have data collection completed and papers published for late Fall 2019.


Smart Trial Logo

SMART-TRIAL is helping Medical Device manufacturers to reduce the chaos and cost of clinical operations by simplifying their clinical data management. Tailor-made for Medical Devices, it’s designed to support a continuous clinical evaluation process throughout the medical device lifecycle. SMART-TRIAL offers DIY electronic data capture with an integrated ePRO system, which allows you to collect structured and high-quality data for both CER and PMS reporting. By providing you with the right tools to manage and collect clinical data, we believe that safer and better devices will reach healthcare faster. Learn more at – Made for Medical Devices.


Castor EDC is a cloud-based Electronic Data Capture platform that enables researchers to easily capture high quality, reusable data for clinical trials and post-market surveillance. The system allows researchers to set up data capture forms, collaborate with colleagues, invite patients through questionnaires, and import, export and analyze their data in a secure, compliant cloud environment, all without elaborate training or technical skills. Through revolutionizing data capture, we aim to make medical research more standardized, compliant and shareable, and to accelerate the development of treatments and cures. Learn more at


Confinis CPM AG logo

Outsourcing clinical investigations allow innovative medical device projects to leverage confinis CPM AG’s senior clinical affairs professionals and senior clinical project managers leadership; therapeutic area and operational expertise; geographic reach; well-established processes; consolidation of subject matter experts and vendors; and validated IT-tools while conserving the project’s own limited resources. Our mission is to deliver the best value in clinical project management.


At this time, there are a variety of sponsorship and exhibition opportunities available for companies wishing to increase their visibility and participation in the program, ranging from keynote speaking opportunities through to exhibitor and documentation sponsors. Organizations most suitable for this type of exposure provide services and solutions including:

  • Survey software
  • EU clinical research consulting services
  • Regulatory consulting services


Eric Jahnke | Sr. Marketing Manager | Q1 Productions
312.955.0424 |