Join nearly 5000 clinical trial professionals and prove your knowledge of GCP quality standards for the Finnish region with Pharmaca's GCP Web Test for the Finnish Market!

With this GCP (Good Clinical Practice) Web Test you are able to prove your understanding of GCP in the Finnish market.

The GCP Web Test was first launched in 2003. Since then, it has helped thousands of professionals stay current with evolving quality standards. The test content is regularly updated – most recently in June 2025, in line with the ICH E6(R3) guideline – to ensure its continued relevance and accuracy.

This test is designed to validate your understanding of GCP standards specific to the Finnish clinical research environment. Whether you're a seasoned professional or new to the field, this test helps solidify key concepts, familiarize you with essential terminology, and clarify the responsibilities of various roles in clinical trials.

This test is in English. If you want to take the test in Finnish, read more here: GCP-verkkotesti Suomen markkinalle.

Would you like to familiarize yourself with the new ICH GCP guideline before taking the GCP test? You can purchase the Perehdytys uuteen ICH E6 (R3) -ohjeeseen webinar (in Finnish) and the GCP web test at a discounted package price! Select the ticket type during registration.

Target group

The online test is suitable for anyone working in clinical trials in the Finnish operating environment:

• Clinical trial managers, research managers, and CRAs in the pharmaceutical industry
• Representatives from CROs
• Healthcare professionals: investigators, research nurses, study coordinators
• Regulatory authorities and ethics committee members
• Healthcare ICT and health tech professionals involved in clinical research
• Patient organization representatives

In this training

• You will learn the key terminology of clinical trials.
• You will learn what the roles, responsibilities, and obligations of different kinds of professionals are.
• You will acquire information about the regulations and laws governing clinical trials.

GCP Web Test is based on the following documents:

• ICH Good Clinical Practice guideline E6(R3)
• Clinical Trials Regulation (EU) No 536/2014
• Act on Clinical Trials on Medicinal Products 983/2021
• Declaration of Helsinki

Certificate

Pharmaca Health Intelligence Ltd keeps a register of all the passed tests. The certificate is valid for three years or until the quality standards change. To pass the test, you need at least 80 % of the maximum score.

TransCelerate BioPharma Mutual Recognition

This ICH E6 GCP Investigator Site Training meets the Minimum Criteria for ICH GCP Investigator Site Personnel Training identified by TransCelerate BioPharma, Inc. as necessary to enable mutual recognition of GCP training among trial sponsors.

Registration and price

The price of the online test is 215 € (+ VAT). The completion time is 31 days from registration.

After registering, you will receive a confirmation email with instructions on how to log in to the online learning environment using your personal user account. Before taking the test, it is important to familiarize yourself with the source materials in the e-learning environment.

The test is in English and consists of 30 multiple response questions, which take a total of about 1–2 hours to answer. You need 80 % of the maximum score to pass the test. After passing the test, you can print or save your certificate. 

The price includes:

• Instructions and materials in electronic form
• One retake opportunity
• Printable certificate of passing the test.

Group registrations:

Request an offer for unlimited organization access or a larger group here.

Please read the change and cancellation terms before registering under: Instructions for participants. Pharmaca reserves the right to make changes to the course.

You can easily pay for this training using a credit card, online payment, or mobile payment, as well as by invoice (companies). The invoice will be generated automatically based on the information you provide and will be sent 1 to 4 weeks before the training date/after registration. Invoicing fee of 15 euros plus VAT at 25.5 per cent will be added to the invoice. Please also include any possible PO number when you register.