We would like to invite clinical specialists to the Basic course for Good Clinical Practice (GCP), that will take place in correspondence format . We will talk about main aspects of clinical trials and you can ask any questions. Course will be in Russian language.
GCP sertificate:
In the eng of GCP course all participants will collect Certificate of GCP, that allow to work in Clinical Trials.
Lecturer:
GCP course will be lectured by Alexey Butylin - MD, PhD, Managing Director of Moscow filial of Crocus Medical BV (The Netherlands).
Programm of Basic GCP course:
Day 1 |
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Perticipants acquaintance. Introduction of GCP course programm. |
Types of medical products. Structure of typical pharmcutical company. |
Pre-clinical studies of medical drugs. Clinical trials classification. |
History of legal regulation of clinical trials. Declaration of Helsinki. History and goals of GCP rules foundation. What is GCP-English and how to use it? |
Rights and duties of Sponsors, contract research organisations, investigators and patients. Providing of clinical trials in details. Procedure of informed consent subscribtion. |
Day 2 |
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Providing of clinical trials in details. Initiation visit. Investigator file and different documentation. |
Providing of clinical trials in details. Monitoring. Handling and storage of study drug. Rules of CRF completion. |
Completion of clinical trial. Finalizing visit. |
Serios adverse events in clinical trials. |
Control questions. Sertificate issuing. |
Participation fee:
Country | Participation fee |
---|---|
Russia | 6 000 Roubles |
Kazakhstan | 29 000 Tenge |
Armenia | 37 600 AMD |
Azerbaidzhan | 126 AZN |
Other countries | 70 Euro |
How can you register to the Basic GCP course:
You can register to the Basic GCP course by two main possibilities:
Possibility 1:
If you are interested in participation in GCP course, please let us know by e-mai gcptrial@crocusmedical.com. We will include you in pre-qualification list.
Possibility 2:
You can sign contact form below and we will contact with you.