Regulatory advice and support

Regulatory advice and support in clinical studies

Clinical studies are subject to extensive laws, regulations and international guidelines. These regulatory frameworks aim to protect research participants and ensure that studies are conducted with high quality, transparency and ethical standards.

In order for a clinical study to be initiated and conducted, approvals and notifications to several authorities and other bodies are often required. Regulatory matters can therefore be both complex and time-consuming.

Our research support

We provide advice and support throughout the entire study process regarding regulatory requirements and applications to relevant authorities for all types of clinical studies.

Related information

• The research process – from idea to archiving
• Templates and supporting documents for clinical study implementation (in Swedish)