Quality in everything we do.

HolyMed Pharma LLP is certified to ISO 9001:2015 and WHO-GMP. Our medicines are manufactured at WHO-GMP certified facilities, under standard operating protocols that run from raw material procurement through to finished product.

HolyMed Pharma LLP ISO 9001:2015 certificate of compliance

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ISO 9001:2015Quality management system certification for HolyMed Pharma LLP.

Certificate number: QMS-2021-Q457331
Issued: 18 June 2021
Valid until: 17 June 2024
Issued by: Quality Assurance & Advisory (QAA), accredited by QAICB

Scope Manufacturing and trading of pharmaceutical products, surgical products, API and drugs, cosmetic, medical and healthcare products.

HolyMed Pharma LLP WHO-GMP certificate of compliance

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WHO-GMPGood Manufacturing Practice compliance, assessed against World Health Organization norms.

Certificate number: WGMP-47WQ-57341
Issued: 18 June 2021
Valid until: 17 June 2024
Issued by: Quality Assurance & Advisory (QAA), accredited by QAICB

Scope Manufacturing and trading of pharmaceutical products, surgical products, API and drugs, cosmetic, medical and healthcare products.

Analytical testing

What we test, batch to batch.

HolyMed has a tie-up with a laboratory where batch-to-batch analysis is carried out using advanced HPLC method. The following checks are conducted routinely.

Compound assayConfirms the active ingredient is present at the declared strength.

DisintegrationVerifies the tablet breaks down within the specified time.

DissolutionMeasures how the drug is released into solution.

StabilityOngoing studies supporting the assigned shelf life.

FriabilityChecks the tablet withstands handling and transport.

Drug distributionConfirms the active is evenly distributed through the batch.

Uniformity of contentVerifies dose consistency from tablet to tablet.

HPLC batch analysisBatch-to-batch analysis carried out by advanced HPLC method.

Our approach

Standard protocol, end to end.

We follow standard operating protocol for the procurement of raw material through to finished product, taking care of every parameter along the way. Good Distribution Practice is applied at all levels, so that what leaves the plant reaches the pharmacy in the condition it should.

Raw material controlIncoming material quarantined, sampled and released against specification.

In-process checksParameters recorded at each manufacturing stage, not only at release.

Good Distribution PracticeApplied at every level of the supply chain.

Need our certificates?

Copies with certificate numbers and validity dates are available on request for distributors, institutions and procurement teams.

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