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ADVENT BIOSERVICES
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CONTRACT DEVELOPMENT & MANUFACTURING ORGANISATION (CDMO)
Your ideal partner in cell therapy
Advent Bioservices began activity as a cell therapy Contract Development & Manufacturing Organisation (CDMO) in 2016. We are currently managing the development of a state-of-the-art facility for multiproduct Good Manufacturing Practice (GMP) production outside Sawston in Cambridgeshire, which will allow scale up of current commercial production and initiate the provision of contract manufacturing services to meet the growing demand for such services in the UK.
The Sawston facility is perfectly positioned in the ‘UK golden triangle’ for cell and gene therapy, our facility is located just 7 miles outside Cambridge city centre with excellent transport links to Central London, London Stansted airport and it is 4 miles from the M11 motorway, linking to the Midlands by the new A14 extension.
The facility consists of 2 separate GMP suites with grade B/C classified areas, in house QC testing, process development laboratories, warehouse and office space as well as a multipurpose cold storage and cryogenic storage unit.
We operate the facility under a comprehensive IT infrastructure including EMS, eQMS eBMR and LIMS systems with secure storage for client documents and paperless systems. Our cleanroom suites are fully validated, with an in-house environmental monitoring system. Clients utilising our manufacturing service will benefit from ancillary services and technical support inclusive of process development, QC and validation. Ultra-cold and cryogenic facilities are available to external clients as off-site storage and are fully GMP compliant.
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Why Choose Us?
Important values we share with our partners...
SCALABILITY
We can help you solve your scale up difficulties and can support your expansion across multiple areas including research and development, process development, higher volume manufacturing and meeting regulatory standards.
EXPANDED
POTENTIAL
We can develop to meet your need, wherever they are. With our global mindset, Advent Bioservices can break down borders ensuring the best possible outcome at every stage of your journey.
REGULATORY COMPLIANCE
We operate to the highest industry standards with expertise in regulatory standards including HTA, MHRA and JACIE. We are GMP and GLP compliant and strive to reach the best quality output. We are here to help you ensure that your process complies with relevant standards.
THE PERSONAL TOUCH
The Advent Bioservices team is conscientious, professional and easy to communicate with. We nurture our business with respect for our clients needs. We have a happy and healthy business culture.
DISCOVERY
Research and development plays a vital part in the advancement of the growth of the cell and gene therapies industry. We can help you by focusing on innovation and optimisation, attending to your individual requirements.
CULTURING PARTNERSHIPS
In the complex biosciences industry, having people that you trust is essential. Our priorities are focused on building long-term partnerships and supporting our clients.
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Services & Facilities
The UK cell and gene therapy industry is expanding at a rapid rate. In the last 5 years, cleanroom space increased annually to a current total of 7819 sq m and the UK initiated 112 new ATMP clinical trials - the highest number for all European countries. This has resulted in strong demand for GMP manufacturing services, expertise in commercialisation and scale up of manufacture.
See what Advent BioService has to offer below.
