Pharma CDMO Services
Biopharma Group's highly experienced team of scientists provide a wide range of end to end, contract R&D and pharma CDMO services. We aim to work alongside you throughout the entire process – from R&D through to validation, verification and manufacturing.
Biopharma Group is equipped to provide aseptic manufacturing for global customers within the pharmaceutical, diagnostic, medical device and biotech sectors internationally. If you do not have access within your own facility, our comprehensive services aim to assist in product and process optimisation, cycle development, product troubleshooting and scale-up.
We also maintain the capability to provide pharma CDMO formulation development services to help improve the stability of a formulation - ensuring that a product is stable in a liquid and/or freeze-dried format and aiding in excipient selection.
We are proud to have a team of experts able to provide specialist support, educated to PhD level in freeze drying, and/ or related sciences - ensuring our work is of the highest standard and quality, informed by individuals who are consistently active within the industry.
Download a copy of our Pharmaceutical Services & Solutions overview brochure, click here
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
GMP Clinical Manufacturing Services
- Clinical GMP Manufacturing Facility
- Formulation & Process Development
- Controlled Class C Preparation
- Clinical Manufacturing Capabilities & Capacity
- Technical Transfer Activities
- Sealing & Packaging
- Final Product Testing