About Z-Jans Pharmaceuticals | Our History & Expertise – Z-JANS HEALTH CARE

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About us

For more than two decades, we have continued to evolve across pharmaceuticals, specialised medicines, consumer healthcare and nutraceuticals — guided by quality, innovation and a strong understanding of changing healthcare needs.

Built to Evolve.

Our story is shaped by a willingness to move into new categories, build new capabilities and look beyond conventional boundaries.

Z-JANS was founded in 1998 with a clear ambition: to build a pharmaceutical company driven by quality, innovation and a strong understanding of evolving healthcare needs.

Our journey beyond Pakistan began in 2001, when we entered the export market and started building the foundation for a broader international presence.

In 2002, we expanded further into specialised pharmaceuticals with the introduction of Ziclopil 4, developed for the management of migraine. This reflected our early focus on identifying specific healthcare needs and developing products within specialised therapeutic categories.

A year later, in 2003, we entered the sweetener category, becoming one of the early pharmaceutical companies in Pakistan to introduce a dedicated sweetener range. This marked an important step in our evolution beyond conventional pharmaceuticals and into emerging areas of consumer healthcare.

As our pharmaceutical capabilities expanded, Z-JANS progressed into more specialised therapeutic areas. This included the manufacture of URO-Z, a hydroxyurea-based anti-cancer medicine, marking an important step in the development of our specialized pharmaceutical portfolio.

In 2015, we expanded into nutraceuticals, broadening our focus into nutrition, supplementation and everyday well being while continuing to strengthen our pharmaceutical portfolio.

MANUFACTURING CAPABILITIES

Experience across multiple dosage forms and therapeutic categories.

Our manufacturing portfolio spans a broad range of pharmaceutical formats, enabling us to serve diverse healthcare needs across established therapeutic areas.


Injectables

NSAID & analgesic, opioid analgesic, antifibrinolytic & hemostatic, Vitamin B12 & neurotropic, antibacterial & antibiotic, third-generation cephalosporin, antiprotozoal and anti-inflammatory categories.


Capsules

Antidepressant, hemostatic, antifungal, analgesic & anti-inflammatory, antibacterial & antibiotic, hematinic, antiulcer and gastrointestinal categories.


Tablets

Analgesic, antidepressant, antibacterial, anxiolytic, antiallergic, neurotropic, hematinic, gastrointestinal, antidiabetic, antifungal, antiemetic, antiasthmatic and antimalarial categories.


Syrups & Liquids

Anthelmintic, bronchodilator, gastrointestinal, antispasmodic, analgesic, hematinic, antiallergic, antitussive and antipyretic preparations.


Creams, Gels & Topicals

Dermatological, antifungal, antimicrobial and antibacterial topical preparations.


Dry Suspensions

Antifungal, antibacterial & antibiotic, and antimalarial preparations across dry suspension formats.

QUALITY CONTROL & LABORATORY

Quality built into every stage.

Our Quality Control department supports product quality from the evaluation of incoming materials through in-process testing and finished-product analysis.

Quality Control Structure

The department is supported by a dedicated team of 17 QC personnel, led by the Head of Quality Control / Manager QC.

  • Raw material, packaging material and in-process sample testing
  • Finished product, water and stability-sample evaluation
  • Analytical method validation and verification
  • Calibration and qualification support

Key QC Responsibilities

Our Quality Control activities extend beyond routine laboratory testing and include:

  • Investigation of Out-of-Specification (OOS) and Out-of-Trend (OOT) results
  • Preparation and review of specifications, SOPs and analytical reports
  • Environmental and microbiological monitoring
  • Maintenance of laboratory records and Certificates of Analysis (COAs)

Laboratory & Testing Capabilities

Our QC laboratory is equipped to perform chemical, physical, instrumental and microbiological testing of pharmaceutical materials and products.

  • Assay, identification, dissolution and disintegration testing
  • pH testing and evaluation of related substances / impurities
  • Microbial limit testing and sterility testing
  • Bacterial endotoxin testing and environmental monitoring

Qualified QC Professionals

Our Quality Control team includes professionals qualified in Pharmacy, Chemistry and Microbiology.

  • Training in Good Manufacturing Practices (GMP)
  • Training in Good Laboratory Practices (GLP)
  • Analytical procedures and laboratory safety
  • Pharmaceutical documentation and relevant pharmacopoeial requirements