Welcome
to Pharmora
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.
Please visit our About us page
Click here to hear from Pharmora Limited’s Stephanie Jones and Ian Pinches as they discuss the benefits of attending the World Drug Safety Congress 2024 and what they do at Pharmora Limited
We were awarded a Silver Medal for sustainability by Ecovadis in 2023.
Our Sustainability page can be found here!
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Our Mission: Quality without compromise
Pharmora is a preferred strategic partner for the following services:
Clinical Development
Pharmora can provide medical and scientist expertise to support your clinical development projects at all phases and through regulatory submission to approval. Click here for Clinical Development case studies.
Patient Safety
Pharmora was built on a foundation of safety expertise throughout the product life cycle. Click here for safety case studies.
Medical & Regulatory Writing
Pharmora can work seamlessly with your team to evaluate the data and ensure the documents accurately convey your key messages.
Training and more
Pharmora runs training courses on key skills and can provide bespoke training packages depending on your needs.
Where are you in your product life cycle?
Pre-clinical
Early clinical development
Phase II-III clinical
development
NDA / MAA submission
Life cycle
management
Pre-clinical
Early clinical development
Phase II-III clinical development
NDA / MAA submission
Life cycle
management
Our latest thinking
The Windsor Framework
Urgent reminder of the Windsor Framework: the deadline is approaching! This is especially important for all medicines manufacturers with a current PLNI and PLGB licence. They need to urgently to cancel their PLNI to be automatically converted to a UK licence. Read on to find out more…
The importance of reporting adverse events
Have you ever experienced an adverse event after taking a medication? Did you tell a healthcare professional about it? Would you know how to report it? Read on to find out why it is important to report!
What is the summary of product characteristics and how does it help me?
The theme for #medsafetyweek2024 is “The importance of using medicines correctly to prevent side effects”. In order to do this we need some information on correct use. Where do we find this? Read on to find out!
Contact Pharmora
Please leave your contact details and let us know how we could help you, whether it is a request for a proposal for our services or an informal discussion to find out if we can support you in any way.