PRA International

PRA International

CroMedica is an international, full-service contract research
organization providing all aspects of drug development services
for Phase I to IV clinical trials. Our philosophy is to foster
partnerships and collaboration with sponsors and investigative
sites to achieve high-quality, rapid, cost-efficient drug
development. As the trend toward outsourcing continues,
pharmaceutical and biotechnology companies are placing
increasing emphasis on outsourcing skills and processes to
competent, professional partners in the drug development
process. A mid-sized CRO such as CroMedica provides the
integrated services, resources and experience of a larger CRO
yet remains personally committed to the success of each clinical
trial.

Our corporate history is testament to the value of this vision.
From a two-person team in 1996 in its first operating year, to a
staff of approximately 350 in the year 2000, the CroMedica Group
of Companies has experienced tremendous growth. Our clinical
trial capabilities now span the globe, encompassing five out of
seven continents. Careful resource planning has ensured that the
quality of our services has matched the pace of our corporate
expansion. This is reflected in our clientele since inception,
over 90 per cent of our first-time clients have returned to
CroMedica for their ongoing clinical research needs.

Company Details

Year Established: 1995

Number of Employees: 356

Company Information

Cathy Schmidt
Title: Administrator
Telephone: (250) 480-0818
Fax: (250) 480-0819
Email: Click Here

Gail Gillis
Title: Director
Area of Responsibility: Domestic Sales & Marketing
Telephone: (613) 739-8162
Fax: (613) 739-8163
Email: Click Here

Paul Gross
Title: Vice President
Area of Responsibility: Domestic Sales & Marketing
Telephone: (619) 558-3888
Fax: (619) 558-3889
Email: Click Here

Services

Clinical Trials

Service Menu Service List: - drug development strategy - protocol design - case record form preparation - regulatory submissions - clinical trial supplies management - investigator recruitment and contracts - investigator meetings and staff training - project management and monitoring - medical monitoring - pharmacovigilance - data management and analysis - medical writing - phase I/IIa research facilities - quality assurance