Pharma CDMO Services
When developing pharmaceuticals, it is vital that liquid and freeze-dried formulations are created to the highest levels of quality, stability and cost-efficiency. This is not easy – particularly with the complex regulatory requirements of drug development and its equally challenging budgets and timescales.
By partnering with Biopharma Group, you can ensure that your liquid or freeze-dried products are created swiftly, accurately and in full compliance with industry standards. We offer end-to-end CDMO services that support every stage of your product’s development – including product assessment, proof of concept, formulation development, cycle development, scale-up, technical transfer and troubleshooting.
From cell therapy applications to clinical trial contexts, we offer a host of flexible CDMO contracts that meet the unique requirements of your operations. These reduce cold chain logistics, improve batch yield and extend product shelf life, enabling you to optimise product performance and ensure return on investment.
Research and development (R&D) projects conducted by the scientific team have delivered:
Average reduction in storage costs
Average reduction in production costs
Average increase in productivity
Average reduction in lyophilisation cycle length

Why choose Biopharma Group?
Drawing on over 35 years of experience in developing liquid and freeze-dried formulations, Biopharma Group is an established and trusted provider of lyophilisation services for the pharma industry. Since 1989, we have completed more than 4,000 projects in over 30 countries worldwide, helping pharmaceutical companies to improve patient care on a global scale. Our specialist in-house commercial and expert scientific teams use this experience to de-risk your drug development timescales, while ensuring that all products created are stable, accurate and robust.
By selecting Biopharma Group as your CDMO partner, your operations also benefit from:
Biopharma Group’s pharma CDMO services are offered at competitive rates, helping you to minimise your drug development costs.

R&D / Analytical Services
- Formulation & lyo-cycle development
- Proof of concept studies
- Design space, tech transfer & scale-up
- Material characterization
- Specialist analytical services – FDM, DVS, SEM, XRD
- Ad hoc consultancy
- R&D Services at a Glance

Clinical Manufacturing Services
- Clinical Manufacturing Facility
- Formulation & Process Development
- Controlled Class C Preparation
- Clinical Manufacturing Capabilities & Capacity
- Technical Transfer Activities
- Sealing & Packaging
- Final Product Testing