Clinical trials conduct is an important milestone in drug development.
«BioEq» is dedicated to the conduct of early phase, late phase and bioequivalence studies.
«BioEq» performs all phases of clinical trials:
- Phase I studies
- Bioequivalence studies
- Phase II-III clinical studies
- Scientific research
- Clamp clinical studies
We also perform the following types of clinical trials:
- Different ways of administration/different dosage forms
- Drug, or alcohol interactions
- Food influence (fasted/fed)
- Age/gender influence
We have dedicated departments at «BioEq» which specialize in different types of the trials:
- Department of Healthy Subjects Studies
- Somatic department
- Oncology department
We have an excellent team of investigators, co-investigators, nurses and coordinators.
Our team experience in clinical research exceeds 15 years.
A standard clinical trial team would include:
- A Principal Investigator or PI
- 5 sub-investigators
- 1 study coordinator
- 3 data entry operators
- 2 nurses
- 1 pharmacist
- 1 medical writer
To learn more about clinical trials expertise provided by «BioEq», please visit the Experience section.
Clinical studies are conducted in accordance with ICH GCP (Good Clinical Practice) Principles and Standard Operating Procedures, which ensure high standards of clinical study conduct.
«BioEq» have well-developed processes and procedures for main clinical trial activities.
«BioEq» SOPs, Quality Management System, automated procedures guarantee high level of quality in clinical trials, good Protocol compliance and speedy study subject enrollment. For example,
- «BioEq» was a top enroller in 2 oncology trials in Russia.
- «BioEq» was a global top enroller in a multicenter trial in NSCLC.
The site has its own Local Ethics Committee which gathers every 2 weeks and upon request.
Preliminary LEC expertise of clinical study documents is possible prior to a study approval by the Ministry of Health of the Russian Federation, which helps to speed up the process of study initiation at the site.
Agreement approval takes maximum of 1,5 weeks.
The list of ongoing studies includes more than a dozen of clinical trials.
Through its partners, «BioEq» can offer integrated support services to efficiently and seamlessly achieve clinical study goals.
91% Sponsors choose «BioEq» for their next trial.
To perform a study feasibility at «BioEq» please send your request to Corporate Development Department of «BioEq» at email@example.com.