What do we believe?
Here at Kaysons Pharma we believe that every breathing person has the right to live their life to the fullest. And we are commited for making it possible.
Why Kaysons Pharma?
KAYSONS PHARMA (KP) is manufacturing and expanding portfolio of path-breaking companies.
Innovation is a way of life as we work towards our emergence as a globally respected company in the field of Oral solid, oral liquid and external preparation.
Our Values
“We the employees of (Kaysons Pharma) are committed to achieve excellence in quality standards and always supply the products as per the Global requirements.” “We shall create an environment where each employee contributes to all aspects of our business processes. We shall strive for continuous improvement to meet with customer satisfaction.”
“Kaysons Pharma. (KP) aims for excellence and leadership in Health, Safety and Environment protection. We are committed to protect the environment in which we operate and ensure the health and safety of our employees, community and interested parties.”
Quality Policy
Implementation of quality policy is done through Quality system based on current Good Manufacturing Practices in conformance with national and international regulatory standards. For Quality Management System a Quality Manual is there, the purpose of this Quality Manual is to define the Quality Management Principles & the quality system elements of (Kaysons Pharma ).
This is achieved by a combination of systemic sampling, testing, validation, monitoring and auditing, facility, systems, equipments, instruments, processes trainings and procedures, which can improve the quality of the products through out the shelf life.
Documentation
Documentation is an essential part of the Quality Assurance System. Its purpose is to define the system control, reduce the risk of error inherent in purely oral communication, ensure that personnel are instructed in the details of, and follows, the procedures concerned, and permits investigation and tracing of defective products.
Documentation system includes the history for each batch of product, including the utilisation and disposal of starting materials, packaging materials and intermediate, bulk and finished products.
There is authorised (signed and dated) specification for raw materials, formula of the product, manufacturing method, printed packaging material, final product specification, in process tests, test methods and packaging material.
