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

WHO SHOULD ATTEND

Executives that will find this program of greatest relevance are those currently working to plan for and fulfill post-market clinical research requirements within medical device corporations. Job titles of those executives that will find this program to be most applicable to their professional functions include:

Clinical Research
Clinical Affairs
Clinical Operations
Post-Market
Post-Market Surveillance
Biostatistics
Clinical Quality Assurance

ej_thumb Contact:

Eric Jahnke | Sr. Marketing Manager | Q1 Productions
312.955.0424 | marketing@q1productions.com

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PRIA Healthcare is determined to accelerate the adoption and commercialization of innovative medical devices and procedures. PRIA’s patient access programs overcome investigational and experimental denials by leveraging data, patient rights, and expert case management. PRIA’s HIPAA-compliant CRM pairs a patient-based approach to case management and comprehensive reporting, providing clients with full transparency through PRIA’s patient access portal into the case-by-case adoption of their procedure categorized by payer, and ultimately building a foundational argument for establishing positive coverage policies.

PRIA’s patient access portal, combined with intuitive attention to detail and flexibility, enables PRIA to control the chaos of the environment and design effective, custom solutions for each client’s needs. PRIA’s passion comes from their commitment to give time and good health back to patients in need. Because of this, PRIA is continuously looking for ways to accelerate the adoption and commercialization of the most advanced medical procedures and treatments.

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