Our Mission Statement:
“Quality Without Compromise”
Pharmora provides assured, global medical review services for the clinical development and safety surveillance of 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.
Large Pharma
If you are part of a medium or large global pharmaceutical company, Pharmora can support your clinical development, patient safety, and medical affairs needs. Click here to contact us to can discuss how we can assist you.
Regulatory Agency
If you work for a regulatory agency and require additional support in assessing marketing authorization applications, click here to contact us to can discuss how we can assist you.
Pharmora’s Core Values:
Our Foundation Value
Integrity
We strive to be honest, fair and true to our word in all our decisions and actions.
Assured
Diligence
Boxless
Get it Done
Respect
Our latest thinking:
Unblinded Medical Review (UMR): How does it work in Pharmora?
In a follow up to the blog outlining what unblinded medical review (UMR) means and why it might be needed, this case study from one of the UMR team explains how Pharmora can support with UMR of clinical trial data.
Case Studies – Unexpected Signal Evaluations
Pharmora helped to meet a tight deadline for submitting an application for marketing approval by reviewing multiple signals to support the safety profile.
Case Studies – How Safety Saved a Study
Pharmora safety monitors conducted a signal evaluation that saved a clinical trial from disaster. Read on to find out how!
