cGMP STERILE MANUFACTURING

Small-batch sterile filling for clinical trials

Fast, flexible fill-finish service specifically designed to meet the needs of clinical trials and stability studies.

cGMP PILOT LAB

Process development, stability testing and QC analysis

In-house expertise to support novel drug development from pre-clinical to commercialisation.

CAMBRIDGE, UK

Supporting excellence and innovation

A state-of-the-art cGMP facility situated at the heart of Europe’s biggest biotech and pharma cluster.

Fully operational from Spring 2022

WE ARE CAMBRIDGE PHARMA

The experts in small-batch sterile fill-finish

We specialise in filling batches of 100 to 10,000 units for a range of presentations, including vials, syringes and cartridges as well as custom primary drug containers.

Our state-of-the-art cGMP facility is designed to provide the highest levels of sterility assurance and quality control. It’s equipped to work with small molecules, cytotoxic formulations and large molecules (non-active biologics), and can handle a wide range of solution viscosities, suspensions and gels.

Alongside our cGMP manufacturing facility, our pilot and analytical laboratories allow our experienced scientific team to carry out process development work, analytical method transfer and validation, QC release and stability testing, and, if required, QP release to clinic.

To find out how we can help you, speak to our project management team today:

Call: +44 1223 736 320

Email: info@cambridgepharma.com