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