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
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.Â
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
Understanding Gaucher DiseaseÂ
Gaucher disease is a rare genetic disorder caused by a deficiency in the enzyme glucocerebrosidase, leading to a harmful buildup of fat in cells. This causes symptoms like enlarged organs, bone pain, and, in some cases, neurological impairment. Current treatments offer relief but come with limitations such as inconvenient infusions, side effects, and the inability to address neurological symptoms. Read on to discover the promising new developments bringing hope for this rare disease…
The MHRA’s Patient Involvement Strategy 2021-25
The MHRA launched the Patient Involvement Strategy 2021-2025. Now, in the final year of the strategy, what has been done for Patient Involvement, and what do the MHRA plan to do next? Read on to learn…
The EMA’s IRIS platform – what is it, and what does it mean for MAHs?
The EMA is transitioning all of the communications during the Marketing Authorisation process to its IRIS platform, read on to learn more about what this might mean for you.