March 17-18, 2017
GCP advanced training
Reserve a place
March 17-18, 2017
GCP advanced training
Advantages
  • A unique opportunity to receive actual insider information about recent trends in clinical trials and to participate in the discussion of significant bias or auditors/inspectors' findings (including Federal Service on Surveillance in Healthcare and Social Development of Russian Federation, EMA, and FDA) during clinical trials in an investigational site
  • You will have an opportunity to prepare for audits and regulatory inspections;
  • An opportunity to fully use modern methods and technologies for the organization of appropriate practice of clinical trials according to ICH GCP principles, local and international laws, at your site;
  • An opportunity to network with colleagues who work in the area of clinical trials.
  • You will receive a certificate confirming the completion of a GCP training registered in Transcelerate Biopharma, the leading international association of clinical studies' Sponsors
For whom is this training:
- Investigational site employees, as well as Sponsor and CRO employees with at least 2 years of experience in clinical trials, who completed basic GCP training during the last 3 years
- The training might be especially helpful for employees involved in the preparation for regulatory inspections (including Federal Service on Surveillance in Healthcare and Social Development of Russian Federation, EMA, and FDA) and audits at investigational sites and CROs
Our team
Key experts in clinical trials conduct, quality
assurance, quality control, and auditing,
members of the British Association of
Research Quality Assurance (RQA)
Dmitriy Manuilov
R&D Head
R&D Head in Maxwell, a Russian company, with significant experience in product development, studies conduction, auditing, construction of quality assurance systems.
Maxim Bunimovich
Independent GCP consultant
QA consultant, trainer (TMQA), with significant experience in audits and inspections of investigational sites in
different countries worldwide, as well as practical experience in the construction of quality management systems for CROs and sites
Maria Leer
Manager
Clinical research quality assurance manager in one the largest global pharmaceutical
companies
Eugeniy Rogov
Independent GCP consultant
Auditor and trainer, former head of the clinical trials quality control of Federal Service on Surveillance in Healthcare and Social Development of Russian Federation
March 17-18, 2017
Two days of new knowledge, methods and hints for your work
Starting at RUR 30 000
The price is RUR 30 000 for a physical
person and RUR 38 000 for legal entities. Group discounts
Best Western Vega hotel
71, bld. 3B Izmaylovskoye shosse
Moscow
Reserve a place
More questions? Send us a message to
trainingcenter@crptrials.com or call
+79218760091
Leaving your data, you agree with the Confidentiality policy
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