Pharmora provides assured, global medical review services for clinical development, filing and safety surveillance of investigational and medical products, from the first clinical trials to ongoing commercialisation.
We have a highly capable team of medics and scientists available to provide flexible and dedicated assured services, at your convenience and within your budget.
Wherever you are in your patient safety journey, from translating pre-clinical data into the first clinical trials, through the development risk management plan (RMP) and safety update reports (DSUR), to your first ever filing and period benefit-risk evaluation report (PBRER), and everything in-between, we are here to support you!
Contact us for a no strings initial consultation to see how we could help you.