Clinical trials are the most expensive aspect of any drug development program. Having the right team on your side will build clarity, trust and efficiency – and ultimately lead to excellent results.
WHY WORK WITH US?
30 YEARS OF CLINICAL RESEARCH EXCELLENCE
Pharmnet has been regarded as a trusted clinical research partner for nearly 30 years. Based in Central Europe, our trials benefit from access to high quality yet cost-effective healthcare with rapid patient recruitment success.
Pharmnet has remained under consistent ownership, which underpins our financial stability and excellent reputation. Our very low staff turnover creates stable, knowledgeable project teams that clients feel comfortable with. These teams comprise highly trained clinical research associates and project managers with long-term experience in clinical trials monitoring and management, including experience in early-phase trials.
- >450 PROJECTS COMPLETED IN DRUG AND MEDICAL DEVICE DEVELOPMENT
- HISTORY OF SUCCESSFUL INSPECTIONS BY REGULATORY BODIES
- CONTINUOUS TRAINING BUILDS DEEP PATHOLOGY INSIGHT
- LOW STAFF ATTRITION (<6%)
OUR PEOPLE – THE CORNERSTONE
OF QUALITY
The majority of the Pharmnet team have more than 10 years’ experience from a wide variety of project types. In this way, Pharmnet has established, and continues to maintain, close relationships with local authorities.
Our staff participate in continuous professional development both inside and outside the company. Through Pharmnet’s own training methods, we share the company know-how to all employees and reward staff for providing advice and support to sponsors/investigators in unexpected and atypical situations.
- GREAT TEAM MEMBERS MAKE FOR A SUPERB TEAM
- ACCURATE CLINICAL EVALUATION MEETS EXCELLENT SERVICE
- COMMITMENT TO LEARNING, ALWAYS
- OUR CUSTOMERS RETURN AGAIN AND AGAIN
QUALITY YOU CAN RELY ON
– AGAIN AND AGAIN
Our mission is to provide highly qualified clinical research services with a commitment to precise, timely clinical trials. We strive for the highest possible data validity combined with clinical subject safety and excellent service.
We are always increasing company knowledge through keeping abreast of new EU regulations, continuous professional development and qualifications, implementation of progressive IT and international collaboration.
CLIENTS AND REGULATORY
AUTHORITIES RECOMMEND US
We value our client and industry relationships and are proud of our reputation. We’ve been recommended as a reliable CRO by both clients and regulatory authority contacts alike.
Several of our clients have worked with Pharmnet for more than 15 years and 90% of our projects are for sponsors who partner with Pharmnet repeatedly.
- STRONG CLIENT/CRO RELATIONSHIPS
- LONG-TERM REPLEAT CLIENTS
AUTHORITIES INSPECTIONS AS THE MIRROR OF HIGH QUALITY, FULLY COMPLIANT SERVICES
Pharmnet projects have been inspected, on average, once a year – by FDA, SÚKL CZ, MHRA, Health Canada, ŠÚKL SK. No critical findings have related to Pharmnet tasks or to site tasks managed/monitored by Pharmnet. In fact, some inspections finished with few or even no findings at all.
MEMBERSHIPS
Pharmnet is a proud member of:
- Association of Clinical Research Organizations of Czech Republic (ACRO-CZ)
- European CRO Federation (EUCROF)
