Glitz Life Care Quality Policy

At Glitz Life Care, quality is a part of our DNA, and therefore, this vision can be viewed in each of our actions. This attribute has enabled us to secure a place in the global market today. A drug or formulation must adhere to numerous parameters to achieve the stipulated quality standards necessary for export and marketing. A number of stringent analysis and tests that are conducted at our organization determine these. The quality is secured through the entire chain from raw material to finished product.

As a long term ethically binding policy, Glitz life Care targets and commits itself to only those products that meet international cGMP standards which leads to the provision of safe, effective and quality products to patients and consumers. To meet this commitment, Glitz Life Care maintains a quality-focused culture to ensure the highest priority being placed on the safety, efficacy and reliability of our products, the safety of our patients and consumers, the quality of data supporting regulatory submissions, and interactions.

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Quality leaders of Glitz Life Care

The quality leaders of Glitz Life Care are meeting this commitment by enabling a quality culture with appropriate systems and procedures in place to operate quality-focused behaviors and ensure decision making relevant to the product’s quality and patient’s safety and satisfaction.

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All the achievements of maintaining the quality standards are concerned to the trained and technical personnel. Providing training to the employees is a regular feature that encourages them and boost their work spirit in addition to inculcate them with recent innovations, technologies and advancements in the international industry.
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Quality Management

Glitz Life Care is strictly bound to implementation of Quality Management Systems and committed towards making continual improvements to the same. Our performance is monitored and regularly reviewed to ensure our standards of conduct meet our high expectations of quality for our patients, customers, and stakeholders.
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Customer Satisfaction

We are making great efforts for achieving customer satisfaction and patient compliance by supplying products meeting various quality parameters and within stipulated delivery time. We anticipate customer’s perspective and support them adequately with all required technical data and information in a time bound manner.

As part of Glitz Life Care’s commitment to Quality:

The Quality Control (QC) department is well equipped with modern instruments and systems for carrying out analysis of the raw materials, packing materials, in-process/intermediate samples, finished drug substances, and microbiological analysis. Approved specifications are applied for the analysis of the products manufactured at the site. Each raw material and packing material manufactured and supplied is analyzed as per laid down specifications.

Quality of water is regularly monitored by chemical and microbiological analysis, and regular feedback is given to the Production, Quality Assurance and the Engineering departments for taking necessary corrective actions, if any.

Quality Control (QC) approves release of raw materials, in-process materials and packing materials only after completing all relevant analysis and found them adequately satisfactory.

Microbiological analysis includes tests for Total Viable Count and for absence of pathogens.

Procedures are also defined for environmental monitoring which includes routine microbiological monitoring of air, surface and personnel in the production area.

Microbiological analysis includes tests for Total Viable Count and for absence of pathogens.

Specifications, standard test methods (Method of Analysis) and acceptance criteria are well documented and revised by the Quality Control department from time to time. All the activities in Quality Control are carried out as per laid down Standard Operating Procedures.

All operations are conducted in compliance with applicable quality regulations, codes and standards;

Department heads are accountable to ensure procedures are in place that adequately define the expectations for work that supports, or directly affects, product quality, product registration and/or data that supports product quality and patient or consumer safety;

All Colleagues and Contingent Workers have the appropriate education, training, skills and experience to carry out their work competently, in accordance with applicable regulations and procedures;

Data and record management is according to the applicable rules and regulations.Processes for escalating issues to ensure product integrity and patient and consumer safety are in place used with consistency.

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