Quality is a never ending process and cannot be achieved easily, but it is a result of dedicated and intelligent efforts of team work in an organisation willing and working in fulfilling and to achieve this objective.
APS Biotech is committed to not only the quality parameters laid down by the regulatory agencies but to exceed the customer requirements and expectations.This commitment is effectively achieved through continual improvements of the Quality Management Systems. To ensure that there is no space of errors, routinely inspection and review of the quality control system is done by the higher management as well as the independent bodies.
In continuation of our efforts to achieve highest quality standards APS Biotech has successfully implemented various Quality Management systems within the organisation.
The manufacturing facility is GMP and ISO certified and conforms with the latest norms laid down by these bodies.
APS Biotech has its own lab with ultra modern facilities and well qualified and experienced people to ensure the reliability of the test reports.
Personnel who come into direct contact in the production activities are medically examined at the time of recruitment and thereafter frequently or as situation demands from a competent medical practitioner.
Only those persons meeting health standards and are medically fit are employed. Personnel suffering from any contagious or obnoxious diseases are not allowed to work or visit in production area.
No toxic or hazardous and sensitizing materials are handled in this facility and the facility is totally enclosed and designed for the exclusive use for manufacturing of Pharmaceutical formulations only.The firm has its own dedicated DM water plant which takes care of the water usage of entire facility. A routine monitoring of water is done drawing samples from various points of usage. The plan envisages that purified water from every usage point is checked once every week for microbiological and chemical tests.