Quality Policy
The Management Team of Triphase and its Employees are committed to adhere to the Quality of our products and stated Quality Objectives.
  • We will maintain a Quality Management System in accordance with the ISO 9001:2008 standard;
  • We will continually improve the effectiveness of our Management System;
  • The Triphase Team will periodically review the performance of our Management System and Quality objectives;
  • This Quality Policy is communicated to all our employees and evaluated by the Management Team for its suitability;
  • Our Employees recognise Triphase as the best organization to work for;

Quality Control and Stability
Triphase Pharmaceuticals' Quality Control department provides support to the manufacturing process through in-process monitoring utilizing a variety of techniques.

Our QC group works closely with the Analytical Development Team to ensure a rapid and seamless transfer of analytical methods as programs progress from process development to cGMP manufacture.

Our in-house dedicated Quality department evaluates your product’s stability and also the process and product consistency. We have the capacity to monitor stability of a product at a variety of temperature and humidity ranges dependent on your intended market.

Quality Assurance
Triphase Pharmaceuticals' provides all the necessary quality and testing support through our own independent quality unit to ensure your product meets international regulatory requirements.
Our Quality Assurance department is responsible for:
  • Ensuring compliance with cGMP and international regulatory requirements
  • Materials and vendor assurance
  • Adherence to customer quality agreement
  • Validation
  • Product disposition
Our quality systems are under continuous assessment through a combination of internal, customer and regulatory authority audits

Analytical Advantages
Our comprehensive range of analytical services supports all of the key activities through the drug development process of your product. These include:
  • Analytical development packages supporting the Development or Refinement of the Manufacture
  • Design, Testing and Validation of cleaning methodologies
  • Development, Qualification and Validation of test methods
  • Characterization of reference standards