GCP & ISO14155
- What is needed to conduct a clinical investigation?
- Who is involved in a clinical investigation?
- What are the responsibilities of the various parties?
- What happens before a clinical investigation and afterwards?
- What are the differences in conduct between drug studies and medical device studies?
These are important issues to which I will provide answers in the most practical way possible. So that after following this training you have not only obtained the answers, but through exercises and practical examples, you are also able to apply the acquired knowledge and translate it into practice, tailored to your situation.
After this training you will be able to:
- Identify what is needed for the design and conduct of clinical research
- Identify the various parties involved
- Have a clear view of the responsibilities of the various parties
- Put the clinical investigation planning in a chronological order
- Identify the differences in conduct between drug studies and medical device studies
Register for this training
By clicking on “register” below, you will see the training dates.
You can enter your details by clicking on the available date.
After receiving your payment, you are registered, and you will immediately receive the invoice.
Time: 2 full days from 9:30 a.m. to 4:30 p.m. incl. lunch. There is enough time between the two training days to perform the practical assignments
Target group: this training lays the foundation for professionals engaged in clinical research with medical devices
Price: €1095,- excluding VAT, per participant
Number of participants: min. 6, max. 12
Certificate: certificate of participation (TransCelerate Certified)
Location: Utrecht region, the Netherlands
Language: the training is provided in Dutch or English. Please indicate in advance if you require the English-language version of the training. The course material is in English.