Our Expertise
Thanet Labs is developing a UK sterile peptide manufacturing platform for contract manufacturing, aseptic fill and finish, lyophilisation, and wholesale supply. Our work is built around controlled manufacture, analytical documentation, and cGMP-aligned quality systems. Specials manufacture and clinical trial supply pathways are planned and will be activated subject to the grant of the applicable MHRA manufacturing authorisation.
Aseptic Fill & Finish
Contract Manufacturing & Development
Lyophilisation
Wholesale Supply
In Development | Clinical Trial Supply
In Development | Specials
Standards
Facilities & Quality Systems
Thanet Labs is being developed around documented quality systems, controlled sterile manufacturing procedures, and analytical verification aligned with cGMP principles and MHRA Manufacturer's Specials Licence expectations.
Controlled Sterile Environment
Cleanroom and aseptic processes designed around controlled environmental conditions, contamination control, documented cleaning procedures, and environmental monitoring.
Batch Documentation
Batch manufacturing records, in-process checks, raw material traceability, deviation records, and supporting documentation maintained according to project requirements.
Analytical Verification
Independent analytical testing available for peptide identity, purity, endotoxin, sterility, and other specification requirements depending on compound and supply route.
Regulatory Pathway
Quality systems developed around cGMP principles and MHRA Manufacturer's Specials Licence expectations, with current and future supply routes clearly defined.
To discuss a manufacturing project, supply requirement, or regulatory pathway, contact Thanet Labs with your project details.
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