FAQ
You may want to become a clinical investigator if you:
have a keen interest in playing an integral role in pharmaceutical and device product development would like to offer additional treatment options or the latest medications to your patients through a research study are interested in new professional and practice-enhancing opportunitiesHow do I become a clinical investigator?
The decision to start working in clinical research requires careful consideration and planning. Consult IFE Baltic Site Development Services for further information.
What requirements must a site meet?
Large parts of the criteria a potential study site has to meet to actually participate in a clinical trial are study-specific and established by the sponsor. In general, possible study sites should:
be reliable be clinically experienced regarding their area of expertise be familiar with ICH-GCP and other relevant regulatory requirements governing clinical trials.
(IFE Baltic offer seminars twice per year) dispose of a database of patients searchable for therapeutic indications and demographic data have an experienced full-time clinical research coordinator able to provide for back-up staff have access to a local or central IRB (Institutional Review Board) obtain IFE Baltic's QA (Quality Assurance)-approval have a favourable history of previous trialsIFE Baltic continues to attract and recruit investigators in Eastern Europe with strong ethics and excellent therapeutic expertise. Combined with IFE Baltic's commitment to high-quality research, its global reach, experienced clinical trial management and support, we partner with you to advance our sponsors' products through clinical development in order to reach the market sooner.
If you are interested in partnering with IFE Baltic to conduct clinical trials, please contact: info@ife-baltic.lt
