Welcome to Yaden Laboratories where we constantly innovate to create quality products with assured safety in fulfilling our promise of wellbeing for everyone.

We are a new-generation Sterile Formulation Finished Dosage Manufacturer. Our state-of-the-art production site, strategically located inside the Katunayake Export Processing Zone opposite Colombo Bandaranaike International Airport (CMB), meets all international industry-imposed modern quality standards.

As Sri Lanka’s largest, privately owned Small Volume Parenteral Products operation, our plant accommodates four dedicated production lines, delivering a range of medicines in the forms of Pre-Filled Syringes, Ampoules, Vials, and Eye and Ear Drops with a production capacity of

As Sri Lanka’s largest, privately owned Small Volume Parenteral Products operation our plant accommodates four dedicated production lines, delivering a range of medicines in forms of Pre-Filled Syringes, Ampoules, Vials and Ophthalmic Drops with a production capacity of

"…. Quality at our best……"

All our products are manufactured under a strict quality code and in compliance with all regulatory standards. Every process at Yaden is streamlined to ensure maximum operational efficiency and absolute safety for both product and personnel.

As a world-class manufacturing facility with expertise spanning cutting-edge drug formulation methods, and an uncompromising quality ethos, Yaden Laboratories is at the forefront of the industry alongside the region’s best pharmaceutical brands.

We are committed to providing innovative, affordable pharmaceutical products of superior quality to customers by ensuring the effective implementation of cGMP compliance.

Our quality objectives are designed to meet:
  • Consistent manufacture and timely delivery of effective pharmaceutical products with premium quality to meet customer expectations.
  • Continual improvement of quality management system through measuring key performance indicators.
  • Create a high quality work culture through effective communication and adequate training.
  • To assure the integrity of our systems and processes.

Our quality objectives are designed to meet:
  • Consistent manufacture and timely delivery of effective pharmaceutical products with premium quality to meet customer expectations.
  • Continual improvement of quality management system through measuring key performance indicators.
  • Create a high quality work culture through effective communication and adequate training.
  • To assure the integrity of our systems and processes.

The facility is designed to manufacture Small Volume Parenteral (SVP) products in order to meet the following regulatory bodies including:

  • National Medicines Regulatory Authority (NMRA – Sri Lanka)
  • United States Food and Administration (USFDA)
  • United Kingdom Medicines and Healthcare Products Regulatory Agency (UKMHRA)
  • European Union Good Manufacturing Practices (EUGMP)
  • World Health Organization (WHO) – Geneva
"….Our State of the Art Modern Facility Features….."
  • BMS (Building Management System), EMS (Environment Monitoring System) designed to monitor and maintain the desired temperature and relative humidity, – Honeywell Trend Software-based approach for recording and review.
  • Cleaning in place, (CIP)
  • Sterilization in Place (SIP)
  • Fully automatic PLC – HMI operated [conductivity based] systems for manufacturing vessels Filtration skid, Filtration vessels, Holding vessels, Product transfer line, and Buffer vessels.
  • Online Conductivity & Online TOC-based monitoring controls in Purified Water generation and distribution system, Water for Injection Generation and Distribution system.
  • Clean room modular partition and ceiling panels with coving – Production & Warehouse areas.
  • Production lines are linear flow automatic featured conveyor operated synchronized machine set ups.

Filling Lines are with the following salient features

  • SCADA (Supervisory control and data acquisition system) integration for all the filling lines
  • Filling servo motors integration with PLC, and HMI for accurate fill volume process to the containers.
  • Control logic interlocks for proper cGMP procedures involve various types of sensors and pneumatic circuits.
“…..Continuous Quality testing……”

reception of the raw materials to sales, in keeping with international regulatory demands.

Ultra-modern Quality Testing Laboratory consists of advanced automated Instruments required for testing and analysis of

  • Raw Materials (API & Excipients)
  • In-process samples
  • Finished Products
  • Stability
  • Microbiological Testing such as
  • MLT
  • BET
  • Sterility