Simson Pharma Global Ltd supplies reference standards, impurity standards, nitrosamine and NDSRI standards, peptide impurities, isotope labelled compounds and custom synthesis products to laboratories across the UK and Europe - with full CoA and characterisation data supporting MHRA and EMA submissions.
Reference Standards
Stock & Dispatch
Traceable Standards and CRM's
Customer Support
Reference materials held in the UK, dispatched domestically.
Laboratories working to a submission deadline lose time at the border. Reference materials imported from outside the UK can be held in customs, and analytical work waits.
We hold stock in the UK and dispatch domestically - no import clearance, no unpredictable arrival window.
UK-registered supplier of pharmaceutical reference materials for MHRA and EMA regulated markets.
Simson Pharma Global Ltd is the UK and European commercial arm of Simson Pharma Limited, India - a Simson company and supplier of pharmaceutical reference materials including drug impurity standards, certified reference materials, isotope labelled compounds, peptide impurity standards and research chemicals.
Registered in Milton Keynes, we support UK and European laboratories with local stock, GBP invoicing and UK-based commercial and technical support.
We supply Inhouse & Traceable Standards that are fully characterised with complete analytical data.
Our catalogue uses EP impurity nomenclature throughout, matching the naming in the monographs UK laboratories work to.
Reference materials and research chemicals for UK pharmaceutical laboratories - over 14,000 products.
Primary, secondary and pharmacopoeial reference standards against BP, Ph. Eur. and USP monographs, with full traceability and characterisation data.
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Process-related impurities, degradation products, elemental and residual solvent standards supporting ICH Q3A, Q3B, Q3C, Q3D and M7 requirements.
Deuterated, 13C and 15N labelled internal standards with documented isotopic enrichment and unlabelled content for LC-MS/MS bioanalysis.
Qualified against characterised reference standards, with assigned potency, traceability records and requalification protocols for your quality system.
Phase I and phase II metabolites, active metabolites and labelled analogues - including synthesis at the scale safety testing requires.
Building blocks, intermediates and specialty organics for pharmaceutical R&D, supplied for laboratory research use only.
Complex organic molecules from milligram to kilogram scale, with route design by PhD chemists. FTE and FFS engagement models available.
Read MoreTrusted by pharmaceutical and research organisations across the UK and Europe.
Reference materials held in the UK and dispatched domestically - no customs clearance, no border delay. UK commercial and technical support in your time zone.
Batch-specific CoA, complete characterisation data and impurity profiles prepared to support MHRA and EMA submissions, with GMP-oriented documentation on request.
Over 14,000 reference materials and impurity standards, spanning pharmacopoeial, non-compendial, nitrosamine, peptide and isotope labelled categories.
Milligram to kilogram scale, route design by PhD chemists, with FTE and FFS engagement models and guaranteed IP protection.
Scientific excellence with regulatory compliance.
To be a leading manufacturer of pharmaceutical reference materials and research grade chemicals in the UK and Europe, recognised for reliability and regulatory compliance.
Deliver time-bound, cost-effective solutions for reference standards, impurity standards, APIs and custom synthesis projects.
Supporting UK and EU pharmaceutical companies with GMP-oriented documentation, Certificates of Analysis and complete technical data packages.
Local regulatory understanding, supply chain visibility and responsive UK-based customer service.
Connect with our UK commercial and support team.
Simson Pharma Global Ltd
4 Fitzhamon Ct,
Wolverton Mill, Wolverton,
Milton Keynes MK12 6LB
Email: sales.uk@simsonpharma.com
Phone:
+44 7788894560
+44 2037701866
Website: www.simsonpharma.com/uk