QUALITY SYSTEM

Quality is our strength and in order to maintain it at every stage of productions we have in house most modern testing Laboratory equipped with all necessary instruments and highly qualified technical staff. Our definition of the word ‘QUALITY’ is what we practice in our everyday life.
Due to company’s aspiration in preserving the high quality of the medicaments it offers, the company has no compromise over the raw materials consisting it’s products, thus importing quality raw materials from reliable sources spreading in lots of countries .

A.R.R. Biotech operate in total compliance with the G.M.P. norms set by the W.H.O. These norms are controlled by a superior hi-tech quality control laboratory divided to three laboratories.

  • Chemical laboratory
  • Physical Laboratory
  • Microbiological Laboratory

QUALITY OBJECTIVES

The quality system shall be observed keeping in mind the following Quality Objectives.

  • To deliver appropriate products within the suitable time frame.
  • To persistently improve through training and development.
  • Continuous analysis of problems and finding suitable solution for sustaining market leadership.
  • To completely do away with rejections and improve productivity.
  • To ensure that the staff puts in their best effort and meet the expected level and parameter of performance.
  • To guarantee that the approved and accepted master formula and analytical procedures are in practice.
  • To ensure that the raw material and packaging materials adhere to the given specification and supplies are through approved vendors.
  • Using market research or survey we decide which product has to be manufactured. Once we reach the decision, the next thing we work is development of product & its specification.

QUALITY POLICY

We are committed to manufacturing Pharmaceutical Products that meet the stipulated standards of Drugs & Cosmetics Act 1940 and conform to the rules mentioned for meeting Customer requirement and producing cost effective quality good.

GMP

The company has a highly functional GMP department managed by well-qualified & skilled team that underwent training by recognized international bodies. The team is managing all GMP/GMP norms at each stage of operation. Besides this the GMP team is providing extensive training to the staff at operational level performing at all levels.

Drug Regulatory Affairs & Quality Systems

Operating all systems in accordance to international regulatory requirements & generation of technical data conforming with regulatory requirements & submission of dossiers to various countries are being managed by well qualified, experienced & trained professionals at international level team.