EXPLORE CAMBRIDGE PHARMA
We specialise in process development and small-batch fill-finish for clinical trials and stability studies.
Our sterile manufacturing facility and analytical labs are purpose-built to meet cGMP and MHRA standards.
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