Quality Policy

We shall produce and deliver to our customers, drugs conforming to clearly established requirements and quality parameters.

We commit ourselves to maintain these through a culture of quality awareness within the establishment based on training and development of all members.

We will further strive to upgrade the quality by improving our work practices and prevention of deviations.


To build capacity and capability to serve chosen markets at globally competitive costs and quality, in time, all the time.


To be a leading manufacturer and a supplier of choice for manufacturing of sterile injectables and other pharmaceutical dosage forms.

Quality Assurance

  • Completely independent function reporting directly to the Managing Director.
  • Comprises of Validation, Quality Management System and In-Process control.
  • All activities of the plant are controlled and released by QA Team.

Quality Control

  • Fully equipped Quality Control lab with all necessary equipments and facilities for all required Tests.
  • Complete Regulatory support for Dossiers, stability studies and Licenses.
  • A separate State of the art Microbiology section with complete facility for sterility testing having 3 sterility rooms.
  • Dedicated Stability Chambers for different temperature and Humidity conditions.
  • Dedicated Control Sample storage area at required temperature conditions.


  • Zen Pharma is WHO-GMP certifiied - click to view copy of certificate
  • Product registrations in Sri Lanka, Costa Rica, Barbados, Bahamas, Ukraine
  • Products manufactured by Zen Pharma are exported to over 15 countries through Marketing partners