Trainings

VST Research offers a wide range of courses to our customers including technical aspects such as monitoring, data-management, medical writing, pharmacovigilance, audits and inspections and also regulatory requirements and guidelines such as national legislation, the Declaration of Helsinki, GCP and other ICH guidelines, plus EU-Directives. These courses can be held in any location in order to meet individual companies’ training requirements.

Our training courses includes:

  • Application to Ethics committees
  • Introduction to Clinical Research
  • Audits and Inspections
  • Medical and Scientific Writing
  • Biostatistics for non-statisticians
  • Medical Devices
  • Biostatistics, Advanced
  • Monitoring, Basic
  • Clinical Study Protocol Writing
  • Monitoring Advanced
  • Clinical trials in the paediatric population
  • Non-Interventional studies
  • Contracts and Agreements
  • Patient Information
  • Effective Site Management
  • Pharmacovigilance
  • EU directives
  • Presentation skills
  • Good Clinical Practice
  • Project Management for Clinical Research
  • GCP update
  • Regulatory Affairs

For more details on our Training Programs, please contact us.

VST Research arranges courses and educational programmes for professionals working in clinical trials. Our courses are directed toward anyone who requires a sound knowledge of clinical trials e.g. employees of pharmaceutical and biotechnology companies and others involved, such as investigators and study nurses. The courses deal with both clinical trials of pharmaceutical and medical device studies. The rules and regulations applied to such trials are often changed and it is vitally important to keep up to date with the changes.

Our training programmes include:

  • Application to Ethics committees
  • Introduction to Clinical Research
  • Audits and Inspections
  • Medical and Scientific Writing
  • Biostatistics for non-statisticians
  • Medical Devices
  • Biostatistics, Advanced
  • Monitoring, Basic
  • Clinical Study Protocol Writing
  • Monitoring Advanced
  • Clinical trials in the paediatric population
  • Non-Interventional studies
  • Contracts and Agreements
  • Patient Information
  • Effective Site Management
  • Pharmacovigilance
  • EU directives
  • Presentation skills
  • Good Clinical Practice
  • Project Management for Clinical Research
  • GCP update
  • Regulatory Affairs

For more details on our Training Programs, please contact us.

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