2008/11/11
Clinical Trials in Russia. 3rd Quarter 2008

2008/9/18
SynRG at the 4th Annual Patient Recruitment and Retention in Clinical Trials conference

2008/9/18
SynRG at the 15th International Pharmaceutical Exhibition "Apteka 2008"

2008/7/24
Clinical Trials in Russia. 2nd Quarter 2008

2008/6/30
A Russian and Pakistani CRO Announce Network Alliance for Expansion of Global Clinical Trials Services

SynRG Clinical Research: Regulatory Affairs

Regulatory support is essential to the drug development process, and SynRG is devoted to serving as a regulatory partner for the success of a clinical development program. Our specialists can offer support in study start-up activities as well as in ensuring regulatory compliance.

Our careful attention to detail and excellent relationship with the regulatory authorities help to expedite the regulatory review process and to shorten drug development timelines. SynRG advisory regulatory service can provide you with help in establishing a strategy for registration in Russian Federation and other CIS countries.

SynRG Regulatory Affairs Service include:

Regulatory submissions in compliance with local requirements;
Confirm presence of all necessary documents;
Review protocol requirements;
Consultancy on the most suitable registration procedure;
Clinical Trial Applications;
Consultation at any stage of drug development;
Coordination with Regulatory Authorities prior and during the registration;
Qualified person for importation of study drugs.

Marya Ilyinskaya,
clinical research assistant

Synergy Research Group (SynRG™) is an emerging CRO successfully assisting both pharmaceutical and biotechnology clients in conducting clinical trials in Russia and CIS countries.