Tukija has published a Guidance Document and Informed Consent Form Template on the use of biological samples and related data in future studies.
The guidance has been prepared for sponsors to consider and apply when consent is requested from participants of a clinical trial for future use of samples and related data.
Swedish and English versions of the guidance and template documents will be published later.
The guidance document and information and consent form template are available on our website: Clinical trials applications in accordance with the EU Regulation (in Finnish).
