Trainings

If you are interested in our training offer, please send your e-mail with enquiry to the following e-mail address: training@brillance.pl.

 

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Training offer addressed to candidates interested in clinical trials career includes: extensive training of ICH/GCP principles, foundation course in monitoring clinical trials phase II – IV and study registration process in Regulatory and Ethics Committee authorities. After finishing each training module, all trainees receive certificate of attendance, which makes way to work as a Clinical Research Associate for CROs or companies from medical, pharmaceutical or biotechnology industry. If you are interested in taking a part in one of our trainings, please send your enquiry by e-mail. We’ll contact you and provide all needed details regarding our training offer including price-list and detailed schedule of trainings & agendas.

• Investigators / Study team members

Training offer addressed to Investigators and study team members includes: basic or advanced theoretical ICH / GCP principles training and extensive course of coordination and conducting of clinical trials phase II - IV according to ICH / GCP, responsibilities and roles of study team members, site preparation for clinical trial related activities, safety of patients participating in clinical study, ethical and legal aspects of clinical trials, source documents / subjects medical records requirements, Case Report Forms completion. After finishing of training module, all trainees receive certificate of attendance. If you are interested in taking a part in one of our trainings, please send your enquiry by e-mail. We’ll contact you and provide all needed details regarding our training offer including price-list and detailed schedule of trainings & agendas.