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Quality

Quality that builds trust.

HolyMed Pharma is an ISO 9001:2015 and WHO-GMP certified organisation, with quality built into how we select products, choose manufacturing partners and document every step.

2Certifications held

8Batch tests run

2029Certified until

HPLCBatch-to-batch analysis

Quality commitment

Our commitment to quality.

Product qualityProducts manufactured through appropriate quality systems and processes.

Manufacturing standardsSelected manufacturing partners, chosen against relevant quality and regulatory requirements.

Documentation & traceabilityProduct and quality documentation maintained for transparency and accountability.

Continuous improvementSystems, processes and professional practices improved as we grow.

Patient & HCP focusProducts and information that support the needs of healthcare professionals and patients.

Quality is not a destination. It is a commitment we maintain every day.

Certifications

Recognising standards. Demonstrating commitment.

Certificate details shown exactly as issued.

HolyMed Pharma LLP ISO 9001:2015 certificate of compliance, certificate number QMS-2024-0227Y47311, valid until 28 September 2029

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

Certificate number: QMS-2024-0227Y47311
Issued: 29 September 2026
Valid until: 28 September 2029
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, certificate number WGMP-0227WQ-47321, valid until 28 September 2029

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

Certificate number: WGMP-0227WQ-47321
Issued: 29 September 2026
Valid until: 28 September 2029
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.

Manufacturing

A partner-based manufacturing model.

We work with selected third-party manufacturers, chosen for their quality systems and certifications.

01Product selectionProducts evaluated on defined business, product and quality considerations.

02Partner evaluationManufacturing partners assessed on capability, quality systems and applicable certifications.

03Technical & quality documentationRelevant product and manufacturing documentation maintained as appropriate.

04ManufacturingProducts manufactured to applicable manufacturing and quality requirements.

05Quality controlApplicable quality-control processes and testing performed before release.

06DistributionFinished products supplied through our network across our operating markets.

Analytical testing

What we test, batch to batch.

Batch-to-batch analysis by HPLC through our laboratory tie-up.

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.

Quality enquiry

We are here to listen.

Share the product name, batch number and your concern — every report is reviewed.

Report a quality concern Report an adverse event

Quality at HolyMed Pharma

Do the right things consistently, build trusted partnerships and keep improving.