QUALITY POLICY

Ombiomedic Pvt. Ltd. is committed to the delivery of safe and effective products to patients and consumers, a fundamental element of our Company’s Purpose and Mission.

 Ombiomedic’s Quality Policy is implemented through a comprehensive Quality Management System. Our performance is monitored and regularly reviewed to ensure our standards of conduct meet our high expectations of quality for our patients, customers  

Each person in Ombiomedic is accountable for ensuring product quality, and patient and consumer safety 

We at Ombiomedic’s firmly believe that customer is the king. We work together to bring in health and happiness and enhance the quality of life.

Quality assurance is a wide concept that covers all aspects that collectively or individually impact the quality of the product. That is, the sum of organized arrangements that are made with the aim of ensuring pharmaceutical products are of the required quality as per the intended use.

Quality assurance is a good practice in the manufacture of pharmaceutical products, as it is the process of vouching for integrity of products to meet the standard for the proposed use. It is an obligation that ensures manufacturers meet the needs of end-user needs in terms of safety, quality, efficacy, strength, reliability and durability. Quality is a benchmark of perfection for the end-user.

We have a well experienced qualified & competent dedicated technical persons in Various departments. We have a team of more than 20 persons in Quality Assurance in Om Biomedic Plant -1

                 Objectives of Quality Assurance 

Quality assurance exists to serve a number of objectives that include the following: 

(1)To offer a guarantee that the person who is administering medicine is confident that every unit will achieve the desired effect. 

(2) To protect users for products from possible accidental defect in the manufacture, design, storage as well as usage instructions. 

(3) To ensure the law is complied with to the latter. 

(4) To offer protection of the manufacturing organization. 

Quality Control 

 Quality Control refers to the features and characteristics of a product that bears on its ability to satisfy the needs of the consumer. Features like shape, dimension, composition, strength, workmanship , finish and colour.

Quality control is an essential operation of the pharmaceutical industry. Drugs must be marketed as safe and therapeutically active formulations whose performance is consistent and predictable. • New and better medicinal agents are being produced at an accelerated rate. At the same time more exacting and sophisticated analytical methods are being developed for their evaluation.

The QC department performs following activities: 

• RM/PM analysis
• Finished Products analysis
• In-process Checks
• Stability Studies

The QC activities are managed through four sections: 

• Instrumental Analysis and Finished Products
• Wet Analysis Laboratory
• Microbiological Testing Laboratory
• Packaging Material -Testing Laboratory