Pharmora* provides assured, global medical review services for the clinical development, marketing and safety surveillance of medical products, from the first clinical trials to ongoing commercialisation.

We deliver the capabilities of a Consultant with the scalability & flexibility of a Service Provider, wrapped in the security of full Quality Assurance.

*At Pharmora we serve our global clients from offices in the UK (Pharmora Ltd) and Ireland (Pharmora Global Solutions Ltd).

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 learn more.

Biotech / Investor

If you’re part of a small organisation, such as a biotech company, click here to discover how we can support you. We also assist investors with due diligence on small companies/ assets, whether in development or already on the market.

Regulatory Agency

If you work for a regulatory agency and require additional support in assessing marketing authorisation applications, click here to learn more about how we can assist you.

What can Pharmora do?

 

Pharmora is a preferred strategic partner for the following services:

Clinical Development

Pharmora can provide medical and scientific expertise to support your clinical development projects at all phases and through regulatory submission to approval

Patient Safety

Pharmora is built on a foundation of safety expertise throughout the product life cycle

Medical & Regulatory Review

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 the

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

Pre-clinical

Early clinical development

Phase II-III clinical
development

NDA / MAA submission

Life cycle
management

Our latest thinking

Impact of Clinical Trial Reforms: Global and UK perspectives

Impact of Clinical Trial Reforms: Global and UK perspectives

Pharmora is pleased to present the 2nd blog in the series celebrating Clinical Trials Day! In this blog one of our Trainee Scientists discusses the latest reforms to clinical trials regulation, how these impact medicine developers globally, and how the UK has reacted to this update. Read on to find out more…

read more
The History of Clinical Trials

The History of Clinical Trials

In this blog post to celebrate Clinical Trials Day 2026, we have written a short history of clinical trials as well as the key milestones leading to the standardisation and improvement in patient welfare.

read more
World Autism Day

World Autism Day

In this blog raising awareness of autism in celebration of World Autism Day (2nd April), Dr Arunesh Sil has written about his experience raising his autistic child and all that it taught him about acceptance and patience.

read more