We have been conducting clinical research since 2010.
We optimize and accelerate the withdrawal of drugs and medical products to the market.
We have a permanent staff of highly qualified employees, candidates and doctors of medical, physical, mathematical and legal sciences.
We carry out CI in Russia and abroad.
We cooperate with clinical centers that successfully pass the checks of Roszdravnadzor and audits of international pharmaceutical companies.
We comply with all relevant regulatory requirements at the local and international levels
Завершенных
проектов
Клиентов
становятся
постоянными
Постоянных заказчиков
You can provide only the molecule name, and we will develop the entire strategy for bringing the drug to market: from designing, calculating the sample size, selecting a reference drug, its procurement (in the Russian Federation or import), to writing the final report on the conducted research and submitting it to regulatory authorities.
клинических
центров
городов России,
стран СНГ и
ЕАЭС
Головной офис компании в
Ah ST pays special attention to the quality management system: it conducts trainings for employees, actualizes the current and is working on the development of new SOP, controls the quality of the functionality of each employee, monitors changes in current domestic and international requirements
Constituent and organizational documents
The list of ki (molecule, phase, nosology) and DKI (molecule, type of research) for the entire period of the company's existence
List of SOP
Any other documents on request
And also, look at the list of documents governing our activities:
If another kio did not live up to your expectations, we will take the project from any stage to the work and bring to the desired result. We will conduct an information transference on the study with the preservation of 100% of the data, re -register documents on changing the kio in the shortest possible time.
Специалист по
клиническим исследованиям
24.07.2023 
7 мин
