Expertise

 

At Diamond Pharma Services we are committed to providing high quality strategic and operational services to the pharmaceutical and biotechnology industry. To meet this commitment, we have assembled a team with broad industry experience in the field of regulatory, pharmacovigilance, compliance and pharmaceutical/biologics technical development.

We focus on the following specialist areas:

  • Regulatory Affairs
  • Product Development
  • Pharmacovigilance
  • Compliance and Quality
 

We work with a variety of clients ranging from the completely virtual through to some of the largest multi-national companies. This demonstrates the way in which we adapt to the requirements of our clients whilst upholding high standards of quality and excellence. Whether it is providing a fully outsourced pharmacovigilance solution or interim regulatory affairs personnel, we can assemble a flexible and bespoke team.

In the pharmaceutical and biotechnology industry, remaining innovative is critical to success. We always strive to be a leader in the field by delivering regulatory solutions to companies developing products at the frontier of technology. In 2013 we were awarded an Innovation Award by TOPRA for providing support for the first gene therapy approval in the EU.

Of note the team is experienced in a wide range of product types from small molecule and next generation biologics through to cell and gene therapy products, at all stages of development.

 

Company values

We strive to overcome hurdles with our clients to bring medicines to patients. We do this by hiring and developing the right people and encouraging them to build significant long-term relationships with clients, to help remove barriers to success. We put relationships at the heart of everything we do. We are experts in identifying skills and qualities in our team and match them to our client’s needs to create successful partnerships.

We have a real passion for what we do, coupled with an eagerness to further enrich our team’s wealth of knowledge. We always provide our clients with informed opinions and use this to guide them down the path to success. Our knowledge and expertise allows us to listen to our clients’ ever-changing needs, and tailor our approach to address them. We are creative, adaptable and pragmatic problem solvers.

We are honest and open about what we can and cannot do for our clients, allowing us to develop long-term trusting relationships with them.

 

Locations

Our Global Headquarters in Harlow, UK, is the heartbeat of our business. Based north of London and 15 minutes by train from Stansted airport, this state-of-the-art facility is bespoke designed to meet the needs of Diamond Pharma Services.

 

This location is also at the centre of the Cambridge-Stansted-London (M11) corridor, a world-recognised region of excellence in the Pharmaceutical and Biotechnology sector. Comprising Essex, Hertfordshire, Cambridgeshire and London, this region has given us access to staff with past experience in companies such as Roche, GlaxoSmithKline, Merck Sharp & Dohme, Mylan, Teva, J&J, Amgen, MedImmune, Novartis, Eisai, MundiPharma as well as many other smaller biotechnology companies. Together with our office on the vibrant Cambridge Science Park and an office in central London, our UK locations provide us with access to staff with world class experience in regulatory affairs.

In the event of a Hard-Brexit, Diamond also has offices in Amsterdam and Sofia. Our office in The Netherlands is based at Amsterdam Zuid, a Metro stop away from the stated future location for the European Medicines Agency. The associated legal entity Diamond Pharma Services B.V. ensures business continuity for Diamond in the event of a Hard-Brexit and is part of an ongoing growth plan to increase our presence in continental Europe.

Out of our Boston MA office we have a network of US consultancies and independent consultants that integrate with us and our clients to offer a cohesive and robust coverage for EU and US regulatory pathways.