Join 4000+ 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 first version of GCP Web Test was launched in 2003, and since then, we are proud to say that over 4000 clinical trial professionals have passed this extensive test. When the quality standards change, the questions are updated soon after to keep the test up-to-date and beneficial to professionals. The test has been updated in February 2022.

The aim of this test is to help the understanding of GCP quality standards, make the terminology more familiar and elaborate on different kinds of professionals' responsibilities and duties. It also shows examples of good and effective ways to work in clinical trials in Finland.

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

Need a test for the Swedish Market? The GCP Web Test for the Swedish Market (in Swedish) is now also available. 

Target group

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

• Pharmaceutical industry clinical trial management, research managers, and CRAs
• Representatives of CROs
• Healthcare professionals such as researchers, research nurses and coordinators
• Industry authorities
• Healthcare ICT actors and those working in health technology and device research
• Patient organizations

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 familiarize yourself with examples of good and effective ways to work in clinical trials
• 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 E 6 (R2)
• Act on Clinical Trials on Medicinal Products 983/2021
• Clinical Trials Regulation (EU) No 536/2014
• 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 (R2) 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 190 € (+ VAT). The completion time is 31 days from registration.

Group registrations:

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

After registration, you will receive a confirmation email with instructions of logging in to e-learning environment with 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 38 multiple-choice 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

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

We have expanded the registration features and sped up the invoice processing. In this training, you can use card payment and make a group registrations. When using the promotional code, please check that the final price is correct. If you chose an invoice as the payment option, it will be generated automatically based on the information you provide. Please also add the PO number when registering. Please use the company search on the form as a priority.