State-of-the-art GMP Manufacturing
With our state-of-the-art GMP facility and specialist complex chemistry expertise we are uniquely positioned to support you with the development and manufacture of your product to GMP.
At Biosynth, we are proud of our rapidly expanding portfolio of cGMP chemical products, developed and manufactured by us. We have vast experience in manufacturing and developing products for a range of applications, including APIs, foodstuffs, excipients, process materials, adjuvants and more. As part of our end-to-end CDMO services offering, we can transfer in an existing process from you and move it into the GMP suite, or take the project right from the first idea to the finished product, scouting and optimising in our research labs before transfer to GMP. With outstanding QC and QA support and a dedicated project manager we can act as your partner in development.
At Biosynth, we understand that your needs may change, and we work as your partner with you, whether this be for your GMP development or supporting scale up and validation we can undertake the whole service or the separate parts you need.
GMP Manufacturing Facility
We have invested in a state-of-the-art GMP plant in Switzerland which performs pilot and production runs at a range of scales up to 100 L, as well as small scale API manufacturing. Our flexible facility can adapt to different process designs and scales, which enables clinical batches and bulk production by the same experienced team of experts.
Find out more about our GMP manufacturing here.
Get in touch with our experts to discuss your requirements [email protected]
Key Features of our GMP Facility:
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About Biosynth
Securing Life Sciences Supply Chains - where Chemistry meets Biology, Products meet Services and Innovation meets Quality, Biosynth is at the Edge of Innovation.
With an unrivalled research product portfolio and end-to-end manufacturing services, we are science led and customer focused to solve problems and deliver key reagents at scale and quality. Our expertise and capability runs across Complex Chemicals, Peptides and Key Biologics all from one trusted partner.?
How We Operate
Dynamic and Flexible Partners
work as your partner to deliver what you need when you need it, being ready for the next stage or phase when business requirements, budget or data demands allow it.
High Quality Analysis
Our analytical capability is a key part of our service, with a highly qualified team of QC scientists across all sites to perform in-process control (IPC) and final product testing. GMP batch release testing of each API is performed in our Swiss quality control laboratory.
Regulatory Expertise and Guidance
Biosynth is experienced with the development and validation of many API processes that have been through various stages of regulatory approval. We are proud to have an excellent inspection record and seek to continually improve.
The experienced team with PhD chemists and regulatory experts work with our customers to meet their quality and regulatory needs.
Get in touch with our experts to discuss your requirements [email protected]