Clinical Research Associate – CRA – 12 months program
One-year education program for Clinical trial associates (CRA) is intended for doctors, pharmacists, dentists or persons who have graduated from colleges of some related sciences. Classes are divided into two semesters and takes place on Wednesdays, Thursdays and Fridays after working hours. We pay special attention to the practical part of the training, and all students goes to the practical part of the course in our classroom and afterwards in one of the CRO agencies or pharmaceutical companies. Number of seats is limited to the 15 participants.
Taking online course is also possible.
Study Coordinator education program – 60 lessons
Education program for health-care professionals who works under the direct supervision by PI or/and Sponsor/CRO for the purpose of conducting Clinical Trials. Education is intended for doctors, pharmacists, dentists or persons who have graduated from colleges of some related sciences. Number of seats is limited to the 15 participants.
Monitoring Course – 30 lessons
Monitoring is the act of overseeing the progress of a clinical trial, and of ensuring that it is conducted, recorded and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and the applicable regulatory requirement(s). Clinical trial monitoring is an Integral Component of clinical trial quality assurance process, and critical for GCP fulfillment.
The Course of monitoring is intended for doctors, pharmacists, dentists or people who have graduated from the faculties of some related sciences and who want to work in the CRO industry. Education takes 3-4 days in our classrooms.
Regulatory Affairs Course – short 16 lessons / complete 60 lessons
It is intended for people who plan to work or work in CRO and the pharmaceutical industry, and are engaged in regulatory affairs. The course covers American and European as well as regional regulations, all lecturers are mainly experts from the Medicines Agency and employees with many years of experience in the CRO industry in regulatory affairs. The course lasts 1 day (short) or 2 days (complete).
Pharmacovigilance Course – 30 lessons
Pharmacovigilance is a set of activities related to the detection, assessment, understanding, prevention and treatment of adverse reactions to the drug, as well as new knowledge of the harmful effects of the drug. The course is intended for people who are planning to work or work in CRO and the pharmaceutical industry and deal with pharmacovigilance. Duration of the course is 1 day.
Pharmaceutical waste management Course (new regulations) – one day course
Education is intended for everyone involved in storage, transportation, reporting and other activities related to pharmaceutical waste. Special attention on this education is dedicated to the new regulations on the pharmaceutical waste management. Duration of the course is 1 day.
Good clinical practice Course (GCP), Advanced GCP and Basic GCP Course – one day course
Basic course for all those who deal with clinical trials (either in the pharmaceutical, CRO industry or in the clinical trials team). Basic and advanced GCP courses lasts for one day each.