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Novera Pharma

Quality

Every lot is tested before it is listed.

Our process is built around traceable lots and verifiable documents, with the precision expected of a Swiss company. The details below will be completed with our laboratory partners' information.

From synthesis to shipping

  1. Close-up of white lyophilized powder in a glass vial

    01

    Synthesis and sourcing

    Origin of raw materials and synthesis partner: [À COMPLÉTER]

  2. Gloved hands placing a Novera Pharma vial in an HPLC autosampler

    02

    Independent analysis

    Each lot is sent to an independent laboratory for identity (mass spectrometry) and purity (HPLC) testing. Laboratory: [À COMPLÉTER]

  3. Analysis report on a clipboard next to a Novera Pharma vial

    03

    Release and certificate

    A lot is listed only once its certificate of analysis is received and checked. The certificate is published on the product page.

  4. Open Novera Pharma box with two vials, a certificate of analysis and a shipping label

    04

    Storage and shipping

    Storage conditions before shipping and packaging details: [À COMPLÉTER]

Reading a certificate of analysis

A certificate of analysis (COA) documents the tests performed on a specific lot. Here is what each field means.

Lot number
Identifies the production batch. It matches the number printed on the vial.
Identity
Confirms the compound is what the label says, usually by mass spectrometry (MS).
Purity
Share of the target compound in the sample, measured by high-performance liquid chromatography (HPLC).
Appearance
Visual description of the product, for example a white lyophilized powder.
Test date and laboratory
When and where the analysis was carried out, with the analyst's signature.

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Tell us what you need. We reply with availability, delivery times to your country and the documents for each lot.

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