STERILE BIOPHARMACEUTICAL MANUFACTURING | MHRA LICENSING IN PROGRESS
Capabilities
Sterile
Sterile vial filling under controlled cleanroom conditions with full batch traceability and analytical verification.
Contract Mfg
End-to-end peptide manufacturing from formulation through sterile fill, lyophilisation, and batch documentation.
Manufacturing
Freeze-drying for peptide stability, cake structure, and extended shelf-life in sterile presentations.
Supply
Establishing supply relationships with research institutions, universities, and pharmaceutical development partners. Subject to verification and applicable regulatory requirements.
Planned
Developing manufacturing and documentation capabilities for clinical and research programmes. Subject to applicable MHRA manufacturing authorisation.
Planned
Building quality systems and sterile manufacturing controls for future unlicensed medicinal product supply under the UK Specials framework. Subject to MHRA Manufacturer’s Specials Licence.
Molecules
Synthetic peptide ingredients for research, institutional, and professional supply.
Custom peptide formulations and presentations for research and institutional programmes.
Bioactive peptides for topical formulation and dermatological research applications.
Short-chain bioactive peptides for investigational and verified research use.
Research-grade small molecules and cofactors for R&D applications.
Recombinant proteins and biologic preparations for research and institutional supply.
Resources
Support
Thanet Labs supplies research institutions, universities, NHS Trusts, licensed pharmacies, prescribers, and pharmaceutical development partners. We do not supply individual consumers or operate a retail channel. All supply is subject to institutional verification.
Every batch is accompanied by a Certificate of Analysis (CoA) from an independent accredited laboratory documenting HPLC purity, mass spectrometry identity confirmation, and test acceptance criteria. Batch records and additional documentation are available on request.
Yes. All manufacturing is conducted at our UK-based cGMP facility. UK manufacture provides full supply chain traceability, regulatory alignment, and controlled environmental conditions throughout production.
Minimum order quantities vary by compound, grade, and service type. For supply agreements and contract manufacturing programmes, we establish agreed terms directly. Contact us to discuss your requirements.
Yes. We accept development-stage contract manufacturing enquiries for peptide-based programmes, including process development, analytical method validation, aseptic fill and finish, and lyophilisation. Contract manufacturing services are subject to applicable MHRA manufacturing authorisation.
Use the contact form on our Contact page with details of the compound(s), quantity, grade, and any specific requirements. We will respond with a quotation, lead times, and supply terms.
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