Our Mission Statement:
“Quality Without Compromise”
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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.Â
We have a highly capable team of medics and scientists available to provide flexible and dedicated assured services, at your convenience.
Large Pharma
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Biotech
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Medical Affairs
- Review of promotional material for compliance with regulatory and local (e.g. ABPI) guidance
- Interpretation and development of key messaging from clinical trial or literature data
- Literature reviews
- Target Product Profile development
- Prescription-only medicine (POM) reclassification to pharmacy or general sales
- Line extension support
- Reimbursement packages to support submissions to local agencies (e.g. NICE)
 Contact us to find out how Pharmora can help you achieve your marketing goals!
If you work for a Regulatory Agency
Pharmora can help bring more medicines to the patients who benefit from them, helping the patient and the manufacturer.
Read more to find out how.
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Pharmora’s Core Values:
Our Foundation ValueÂ
Integrity
We strive to be honest, fair and true to our word in all our decisions and actions.
Assured
We promise to aim for the highest standard and guarantee to meet or exceed client expectations.
Diligence
We are conscientious, attentive and persistent in our work, working sustainably for the long-term good of our planet.
Boxless
We are not confined; we seek new ways to excel for our clients.
Get it Done
We are energetic and deliver on-time.
Respect
We have due regard for the feelings, wishes and rights of our colleagues and clients, fully supporting diversity and inclusion.
Our latest thinking:Â
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!
