TFS Academy courses are designed for professionals working within the clinical trials industry and include courses for both pharmaceutical products and medical devices.
TFS Academy 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:
Application to Ethics committees
Audits and Inspections
Biostatistics for non-statisticians
Clinical Study Protocol Writing
Clinical trials in the paediatric population
Contracts and Agreements (Sweden)
Effective Site Management
Good Clinical Practice
Introduction to Clinical Research
Medical and Scientific Writing
Project Management for Clinical Research