Designed to WHO-GMP Guidelines

Quality is built into every step. Our facility follows WHO-GMP guidelines, and our Quality Assurance and Quality Control teams oversee production from raw material to finished pack. Every batch is tested in our in-house laboratory before it reaches pharmacies.

WHO-GMP guidelines

A manufacturing unit designed around WHO Good Manufacturing Practice, regulated by the Department of Drug Administration.

Independent QA and QC

Separate Quality Assurance and Quality Control departments, so the team that checks a batch is not the team that made it.

In-house laboratory

Chemical, instrumental and microbiological testing carried out on site.

Validated processes

Stability studies, process validation and cleaning validation behind every product.

Quality assurance laboratory

Analytical & Testing Capabilities

Chemical & Physical

  • Chemical testingIdentity, purity and strength of raw materials and finished products.
  • Instrumental analysisInstrument-based methods that measure what each dose contains.
  • Microbiological testingChecks that products are free from harmful microbial contamination.

Process Validation

  • Stability studiesConfirm that a product keeps its quality through its shelf life.
  • Process validationShows that a process gives the same result batch after batch.
  • Cleaning validationProves equipment is clean before the next product is made on it.

Regulatory Compliance

  • Manufacturing licenceIssued and renewed by the Department of Drug Administration.
  • Product registrationEach medicine is registered with the DDA before it is sold.
  • WHO-GMP certificationCertified by the DDA against WHO Good Manufacturing Practice.

How quality is organised

WHO-GMP guidelines

A manufacturing unit designed around WHO Good Manufacturing Practice, regulated by the Department of Drug Administration.

Independent QA and QC

Separate Quality Assurance and Quality Control departments, so the team that checks a batch is not the team that made it.

In-house laboratory

Chemical, instrumental and microbiological testing carried out on site.

Validated processes

Stability studies, process validation and cleaning validation behind every product.

A quality control laboratory

Why domestic manufacturing matters

Nepal still imports a large share of its medicines. Every locally made batch narrows that gap.

100+
Allopathic manufacturers operating in Nepal
60%
Of Nepal's medicine market supplied by domestic producers
40%
Still dependent on imports
Rs. 29.3 bn
Of allopathic medicines imported through Birgunj last fiscal year

Sources: Ekantipur, August 2026; Nepal Pharmaceutical Association, Parsa.

60%
Made in Nepal

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