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FharmaGlobal

Quality & documentation

Compliance.

Batch-specific documentation and clear information for each proposed arrangement.

Certificate policy

Ask for the relevant batch.

Batch-specific purity certificates are available on request before or after purchase.

Before purchase, tell us the product and strength so our team can provide the certificate for the batch currently available. After purchase, include your order reference to request the certificate for the batch supplied.

Batches change as stock arrives and is supplied. A certificate for one batch does not describe every batch of that product. Confirm the applicable batch with our team.

Request a batch certificate →
Reading the certificate

Details you can check.

The relevant certificate records the reported purity, batch reference and dates. Read the product identity, batch details, test information and results together.

We provide the issuing laboratory’s report reference and verification details where available. For certificates issued by Freedom Diagnostics, enter the Search Code or Accession Number printed on the report in its COA lookup ↗.

Compare the original report’s product identity, lot, dates and measured results with the documentation for the offered batch. An online report alone does not establish that a particular item belongs to the tested batch; ask our team for the supporting batch information.

A purity result alone does not establish sterility, clinical safety or approval for human or veterinary use.

Product information

Confirm the exact variant.

Product names, formats and total strengths are listed for identification. Total contents are not dosing instructions. Individual ingredient amounts are shown where confirmed.

Certificates describe the reported tests and the identified batch. We do not apply a blanket purity percentage, testing guarantee or regulatory approval across the catalogue.

Supplier requirements

Current, applicable records.

FharmaGlobal works with manufacturers, suppliers and businesses able to provide corporate, quality, regulatory and product documentation relevant to the proposed arrangement and intended market.

Applicable licences, certifications, specifications, quality information and supporting records may be requested and reviewed. Commercial engagement remains subject to satisfactory documentation and appropriate due diligence.

Our role. FharmaGlobal coordinates research-product enquiries and pharmaceutical sourcing discussions. We are not a regulatory authority, certification body or product approval organisation. Supplier review and customer certificate requests are distinct parts of the documentation process.

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