Apr 22, 2014, 00:00
by
Michael Croft
MINNEAPOLIS, MN - Apr 22, 2014 - Regulatory and Clinical Research Institute, Inc. (RCRI) announced that David France has joined RCRI in the role of Principal Advisor
MINNEAPOLIS, MN - Apr 22, 2014 - Regulatory and Clinical
Research Institute, Inc. (RCRI) announced that David France has
joined RCRI in the role of Principal Advisor. Prior to this role,
France served as the Director of Clinical Affairs at St. Jude
Medical.
France said, "I am very happy to join RCRI's highly respected
team of experts and add my experience and knowledge to help our
clients navigate an increasingly complex healthcare landscape."
In his 28 years of experience in the medical device industry (25
years in clinical studies), France has held leadership roles in
clinical affairs, regulatory affairs, and training for both small
and large companies. His extensive knowledge in a wide
variety of clinical and regulatory settings and geographies
includes, but is not limited to, strategic planning (including
Class III active implantable devices), protocol development,
enrollment strategies, report authorship, FDA advisory panel
preparation, extensive site and investigator management, and
publication strategy development and support.
Additionally, France has built and managed numerous clinical
study teams both in-house and in the field and he has utilized his
training expertise to strengthen clinical operations and provide
highly technical product education to physician customers, sales
teams, and field engineers.
Mr. France holds an undergraduate degree in Biology from Gannon
University, and has completed graduate-level science coursework in
Bioengineering at Pennsylvania State University.
For additional information on RCRI, Inc. and its services please
visit: www.rcri-inc.com or email Todd Anderson at
tanderson@rcri-inc.com or call 952-224-2254.
About Regulatory and Clinical Research Institute,
Inc. RCRI is a strategic consulting firm with
comprehensive operational services supporting the medical product
development lifecycle. It specializes in the medical device,
in-vitro diagnostic, biologic, and combination product
spaces. RCRI partners through consulting engagements at the
senior management level to address the most significant industry
challenges in today's global environment. RCRI provides
expert advisors and exact practices in regulatory affairs, quality
systems, clinical research, health economics and market access
(development, entry, and expansion, including technical
reimbursement management). RCRI is quality driven organization and
is ISO 9001:2008 certified.