QA
Quality Assurance
The strict regularoty requirements and the challenges of staying competitive in a fast changing environment is very vital .Quality Assurance (QA) covers all aspects that could have an impact on the quality of prescribed pharmaceutical products and meets regulatory requirements.. It is well known that all manufacturing stages need quality assurance actions to ensure successful results
Om Megashree Pharmaceuticals in relation to Quality Assurance
Quality Assurance Policy
It is our goal to consistently meet or exceed our customer’s expectations and requirements of quality products through continual improvement of the quality management system.
Objectives of Quality Assurance:
To ensure that the prescribed medicine competently provides the desired effect to the person taking it; to protect patients from accidentally being administered an incorrect or contaminated medication; and to ensure medicines comply with the regulation.
At Om megashree , Quality assurance department is responsible for conducting in-process quality checks, documentation and audits. In addition, the officials are responsible for providing on the job training, installation qualification, Validation and meeting regulatory requirements..
Our industry is dedicated to Deliver the highest quality Medicinal products in the pharmaceutical sector.
Our QA team comprises of qualified, experience and technically sound personnels who are proactive to keep control of quality, costs, reliability and speed while also complying with regulations.
Our Quality Assurance takes a proactive approach which ensures that product manufacture adhres to specific standards and strives to continuoulsy improve results and eliminate errors .
In a nutshell products should be ‘ fit for purpose” and right first time. By optimizing process reliability and efficiency, quality assurance brings about speedy and effective operational performance.
Quality assurance also works on lead quality enhancement initiatives, eliminates activities which do not add value, reduce the cycle time required to handle and resolve the quality issues and lessen reoccurrence of deviation