Criterium Press Releases

for Immediate Release
Contact: Arthur Gonick
(518) 583-0095 x 117
aigonick@criteriuminc.com
Criterium, Inc. Opens Office in St. Petersburg, Russia
(New York- 14 June 2007) – Criterium,
Inc. announced today that it has opened a regional office
in St. Petersburg, Russia. The contact information for
this office is:
Address: 197376, Prof. Popov str.
23, Suite 7, Saint-Petersburg, Russia Telephone: 011
7 812 944-84-72 Contact: Svetlana Tsareva, Clinical
Liaison Email: stsareva@criteriuminc.com
This office extends Criterium’s
worldwide clinical trials capabilities in Russia, the
former Soviet Republics and Eastern European States.
The following services will be offered in conjunction
with Criterium’s global full-service contract-research
resources:
- Regional Regulatory Support ·
Site Selection
- Medical and Clinical Trial Monitoring
- Project Management
- Trial Drug Importation and Storage
- Translation of Protocol and other
trial-related forms
- Medical Writing
The Russian and Eastern European region
has proven itself to be increasingly popular with worldwide
pharmaceutical, biotech, and medical-device developers.
They have increased the number of international multicenter
trials in which this region participates by over 400%
since 1998. However, when compared to the number of
trials in the United States and Western Europe, there
remains a large opportunity for future expansion.
The region is characterized by a strong
medical system, universities and academic centers, specialized
hospitals and European standards-compliant legislation,
a large contingent of well-trained and highly skilled
medical personnel, and a history of ICH/GCP compliance.
Furthermore, this region has large potential patient
population pool for many therapeutic areas that are
not able to have access to modern treatments and therefore
are prime candidates to enroll in clinical discovery
programs.
We are enthusiastic about this expansion
and the advantages it will bring to our clients,”
noted Criterium, Inc President and Founder John M. Hudak
“this new office further emphasizes our commitment
to go to appropriate regions throughout the world to
recruit the best patient candidates as rapidly as possible.
Our centralized standard operating procedures for data
management and workflow, combined with highly trained
on-the-ground field personnel for monitoring and regulatory
support, assures that every project we undertake will
continue to be conducted with the highest standards
and in the most
efficient manner.”
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