Your one-stop-shop for project management,
QP certification and Regulatory advice
Our services
We mainly focus on these services, but of course we will also do related services to these fields. Get in contact to see what we can offer.
CMC Project management
To get your compound into a clinical trial, a stable drug product needs to be produced. For this, several development activities need to be performed and we will help you in setting these up
QP services
OctoRelease will make sure that it keeps QA/QP oversight over the clinical supply chain from DS to DP to FDP
QP CERTIFICATION OF CLINICAL TRIAL MATERIAL
OctoRelease is acquiring its own manufacturing license from the Dutch Authorities. Once this is achieved, OctoRelease will have two QPs to certify the manufactured final drug product to be used in your clinical trial.
Regulatory advice
When you start building your clinical trial application, a lot of data needs to be comprehensively documented in the IMPD or IND.
Contact Us
Do you want to schedule a meeting with us or hire us, please get in contact with us.