MCR works in conformity to Good Clinical Practice (GCP) and current regulations. In addition MCR has developed a set of Standard Operating Procedures (SOPs) which are regularly updated to reflect regulatory environment.
MCR offers a comprehensive set of services to provide medical devices and pharmaceutical companies with an integrated solution for product development and approval process.
MCR has a large experience in investigator-initiated trials and can offer logistical and operational support, scientific and regulatory expertise and training.
Meet MCR at EuroPCR 2016
Planned and ongoing clinical trials: a status update from Mediolanum Cardiovascular Research (MCR)
Wednesday 18 May 2016
13:35 - 14:35
CRO / ARO Room 342B
Attend this session if you want:
* To be updated on planned or ongoing clinical trials that may change our future practice
* To gain in depth understanding of trial design and execution
* To learn about upcoming milestones for trial recruitment, analysis and presentation plan