Services

The contract research organization LLC "ClinPharmInvest" offers its customers a wide range of highly qualified services for organization of clinical trials of the I-IV phase, as well as bioequivalence studies, develops a complete package of documents for clinical trials, and provides for quality control of studies and statistical data analysis.

1.

Development of a go-to-market strategy

Evaluation of the promotion method effectiveness, the adjustment by experts of pharmaceutical marketing considering the method effectiveness and its financial feasibility.

2.

Clinical studies of bioequivalence and phase I

Clinical studies of bioequivalence and phase I involving healthy volunteers and patients.

3.

Clinical trials of II—III (late) phases

Determination of dosing level and schedule, patient groups’ sensitivity to different drug doses, drug safety for patients with a particular disease.

4.

Marketing authorization

A study of the specific pharmacological activity of a drug or a new chemical synthesis product on disease models in laboratory animals.

5.

Post-authorization trials and monitoring programs

Evaluation of the promotion method effectiveness, the adjustment by experts of pharmaceutical marketing considering the method effectiveness and its financial feasibility.

6.

User testing

Creation of a final package leaflet that allows the majority of consumers of a medicinal product to make safe and correct decisions about its use.

75-2 Respublikanskaya St., Yaroslavl 150000, Russia
+7 4852 59-47-71, 59-47-79
info@cphinvest.ru