Capabilities
Capabilities and Services
SYNRGY SCITECH offers a focused set of capabilities centred on the pharmaceutical research and analytical supply ecosystem. We support customers across the lifecycle — from early R&D through method validation, through commercial QC and ongoing regulatory work.
API sourcing & supply
Active Pharmaceutical Ingredients sourced and supplied with relevant documentation, supporting formulation, R&D and commercial manufacturing programmes.
Impurity standards
Identified and unidentified impurities — including stereoisomers and degradation impurities — synthesised and characterised for analytical and regulatory work.
Reference standards
Pharmaceutical reference standards for assay, identification and purity testing — supplied with batch documentation suitable for QC use.
Custom synthesis support
Custom synthesis against customer-supplied structures or literature references — feasibility, lead-time and quantity scoped before quotation.
Analytical support
Selected analytical support around method development, validation context, and characterisation — to ensure customers can deploy supplied materials confidently.
Documentation support
Certificate of Analysis, Material Safety Data Sheets, specification sheets, and structure / characterisation data shared transparently.
Regulatory-oriented supply
Materials supplied with the documentation profile required for nitrosamine programmes, impurity profiling submissions, and stability work.
Bulk enquiry support
Multi-batch and bulk supply with traceable batch records, lead-time visibility and ongoing programme alignment.
Stable isotopes & metabolites
Deuterated compounds and metabolites for mass-spectrometry-based bioanalytical work.
How we work
A focused engagement model for technical buyers
Each enquiry is reviewed by our scientific team. We confirm what is genuinely available, identify what requires custom synthesis, and propose a documentation profile that works for your end-use.
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Step 1
Enquiry & scoping
Share the compound, CAS number or structure with intended quantity and use-case.
Deliverable: Technical requirement brief -
Step 2
Feasibility & quotation
We confirm availability, lead time, documentation profile and feasible pack sizes.
Deliverable: Committed commercial & technical quote -
Step 3
Order & documentation alignment
On confirmation, supply planning starts with documentation checkpoints built into execution.
Deliverable: Planned execution + document checklist -
Step 4
Dispatch & ongoing support
Materials are dispatched with traceability, and our team stays available for follow-up technical queries.
Deliverable: Traceable delivery + post-dispatch support
Have a custom requirement?
Send us your specification, structure or CAS number and we will respond with feasibility and a clear path forward.
Send enquiry