Clinical Investigations 101

Are you considering a clinical investigation for your medical device but unsure where to start? Would you like some help figuring out which aspects to outsource and what steps to take before contacting a Contract Research Organization (CRO)?

This short self-study course, consisting of 8 modules, is intended to help those who work with new medical devices and are unfamiliar with the complex world of planning, execution and reporting medical device clinical investigations.

If you are planning a clinical study for your device, this course will equip you with essential concepts and terminology and offer guidance on contacting a CRO that can help your product succeed.

Please note that Clinical Investigations 101 focuses on the investigations of medical devices. It does not cover the specifics of IVD medical device clinical performance studies.

Billing and cancellation policy

Read the billing and cancellation policy for online trainings here.

Participation in the training can be cancelled two weeks (14 days) before the event free of charge. For cancellations made after this, we will charge 50% of the participation fee, except for cancellations made one week before the event, we will charge a 100% participation fee.

Cancellations are always made in writing to: koulutus@labquality.fi.  
The participating organization may, if it wishes, change the participant free of charge by notifying it in writing before the event to:  koulutus@labquality.fi. The participation fee will be invoiced immediately after the event. The training session will be confirmed to the participant by e-mail about a week before the event.  Labquality reserves the right to cancel the training session due to a small number of participants.