SAFC Pharma – Manchester, UK
SAFC Pharma's Manchester, UK facility has 20 years experience in medicinal chemistry, process R&D and cGMP API manufacturing for early-stage development. Our focus on progressing lead compounds to the clinical proof-of concept stage in the shortest time possible.
>> Manchester Facility (pdf)
| We provide: |
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A facility inspected and approved by the Medicines and Healthcare Products Regulatory Agency (MHRA) |
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A 25,000 sq. ft. facility |
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A highly-qualified and experienced team |
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Well-equipped R&D, scale-up and analytical laboratories |
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Excellent track record of success |
| Capabilities |
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Over 30 PhD. qualified R&D chemists |
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Sixty fume-hoods located in three R&D laboratories |
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Equipment and glassware to meet medicinal chemistry requirements |
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A MHRA certificate of compliance with ICH Q7a |
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Four independent cGMP manufacturing suites |
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Scale-up vessels from 20 L to 200 L |
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Comprehensive in-house analytical support |
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| Discovery Services |
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Compound design and optimization services |
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Focused compound library production |
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Building block synthesis |
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Medicinal chemistry specialists |
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| Development and Manufacturing Support |
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Process research and development |
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Scale-up for pre-clinical studies |
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cGMP API production for clinical trials |
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Documentation support for regulatory submissions |
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Metabolite and impurity synthesis |
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Analytical method validation |
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Stability studies |
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