Published on Thursday May 29, 2014
Smooth Drug Development performs GCP trainings
Smooth Drug Development invites you to attend a GCP training organized by Smooth Drug Development, CRO in Russia and CIS. The training title is "GCP: Basics. Practical Aspects of Monitoring in Clinical Trials. Audit and Inspections Findings".
To whom it can be interesting:
- Investigators from hospitals, pharmaceutical companies, and research institutes
- Clinical trials support staff (e.g staff working in contract research organisations)
- Research Nurses
- R&D staff involved in approving and monitoring clinical trials
- Members of ethics committees
- Graduates looking to develop a career in clinical research
Topics: ICH GCP basics, Sponsor's, CRO's, site's and investigator's responsibilities, normative documents, ICF, investigational drug, source documents, ethical aspects, requirements to records keeping, sites' monitoring, subjects' safety, etc.
Duration: 3 days
Weekly from 18:00 to 21:30
Once the examination is passed, we will issue you with a GCP certificate for your records.
Price: 24 500 Rub.
Seats are limited
Additional Information:
Tel: +7 921 913 04 23
info@smoothdd.com