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.
In the eng of GCP course all participants will collect Certificate of GCP, that allow to work in Clinical Trials.
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:
|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.|
|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.|
|Russia||6 000 Roubles|
|Kazakhstan||29 000 Tenge|
|Armenia||37 600 AMD|
|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:
If you are interested in participation in GCP course, please let us know by e-mai firstname.lastname@example.org. We will include you in pre-qualification list.
You can sign contact form below and we will contact with you.