QUALITY POLICY Pacific Pharmaceuticals Ltd. has adopted a policy of producing Quality Products and service in compliance with the regulatory and International Standards that enhance Company’s reputation in the market place by meeting & exceeding the Quality expectation of our Customers and the Consumers.

• Quality will continue to be our major strategic thrust.
• Every employee is a part of our Quality System Team.
• Develop a Quality Management System to ensure Quality of ourProducts and their intended use.
• Develop a climate that allow our Employees to work in a friendly environment.
• Develop a culture of continuous improvement.

HPLC Auto sampler HPLC systems with UV, RI and diode array detector, Agilent 1100 series quick, accurate and precise result.

Potentiometers: Two 718 stat FIP titrator Units used for the dermination of proteolytic activity of enzymes by the potentiometeric titration. One 799 GPT titrino Potentiometer and KF Titrator, used for the potentiometeric aqueous, non aqueous titrations and water content determination

G.C -6890 N Gas Chromatograph used for the qualitative and quantitative analysis of low boiling samples

Dissolution & Disintegration Apparatus Erweka dissolution apparatus used for the testing of dissolution rate of the acitve constituent in the tablets and capsules. Erweka Disintergration Apparatus DT 700 used for the determination of disintergration ability of the tablets and capsules.

The Quality Assurance (QA) department is comprised of the QA Director, QA manager and several QA officers. The QA framework is designed to ensure all manufacturing processes and Quality Control testing conforms to cGMP regulations. The principle responsibilities of QA are:

• Author and review SOPs for technical correctness
• Review batch product records
• Provide training
• Inspect product
• Provide technical guidance to QC