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SYNRGY SCITECH

Quality

Quality and Documentation

A documentation-led approach to pharmaceutical material supply, with clear scientific communication.

Quality at SYNRGY SCITECH begins with how we evaluate and qualify a material before it reaches a customer. Our approach is centred on documentation, traceability and clear scientific communication.

Each product can be supplied with a Certificate of Analysis (COA) that captures the analytical results for the supplied batch — including assay, purity (where applicable), residual solvents, water content, and other key parameters relevant to the material. Material Safety Data Sheets (MSDS) and specification sheets are provided alongside, on request.

We do not make broad regulatory claims that we cannot substantiate. Where customers require additional documentation — such as method of analysis, stability data, or regulatory letters — we work transparently to indicate what is achievable and what is not.

Our quality process

From documentation to dispatch

A clear, repeatable sequence applied to every supplied material — sourced, custom-synthesised or stocked.

  1. Step 1

    Documentation profile defined

    COA, MSDS and specification sheets supplied with the material — clearly linked to the supplied batch and agreed at the quotation stage.

  2. Step 2

    Sourcing & supplier qualification

    Sources are evaluated for technical capability and document availability before onboarding. Established sources are re-qualified periodically.

  3. Step 3

    Traceability throughout

    Batch records and source-of-supply traceability maintained for every material — from inbound to dispatched.

  4. Step 4

    Handling & storage guidance

    Clear, written handling and storage guidance accompanies each supplied item — covering temperature, container and shelf-life expectations.

  5. Step 5

    Scientific communication

    No overstatement of analytical capabilities or regulatory positioning — only what we can substantiate, and we say so transparently when something requires confirmation.

  6. Step 6

    Compliance-aligned response

    Where customers need additional regulatory support, we work transparently to indicate what is achievable and what falls outside of our scope.

Laboratory quality control environment

In the lab

Documentation that matches your QC expectations

Every batch is reviewed against agreed specifications before dispatch — with COA, MSDS and handling guidance supplied where applicable.

  • Batch-specific Certificate of Analysis
  • Material Safety Data Sheets on request
  • Specification sheets for agreed material profiles
  • Traceable records from sourcing to dispatch
A note on certifications

We do not claim certifications we have not earned.

Where you require ISO, GMP or regulatory letters, please ask us upfront. We will indicate clearly which materials are supplied with what documentation, and where third-party documentation is required, we coordinate it transparently with the customer.

Discuss your documentation needs