The indomitable spirit and motivation of the development team is guided and centered on the
sole objective of ensuring that our manufactured products are of the highest quality to achieve
maximum efficacy.
- GOOD MANUFACTURING PRACTICE (GMP): ensures that products are consistently produced and controlled in compliance with quality standards in place, appropriate for their intended use;
- Ensuring best quality products and services to our valued customers;
- Diligent monitoring of our activities as per various regulatory guidelines and continuous development, backed by extensive research activities;
- Promoting health, safety and environment awareness by organizing regular training and various other programs towards fulfilling social commitments and making Cogent environs an ideal and preferred workplace.
- Round the clock monitoring of various systems in place to ensure strict and uncompromised compliance to quality standards of the products;
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;
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. These documents are approved and controlled by the Quality Assurance department. The Quality Assurance department reviews and approves all Standard Operating Procedures before implementation. All the activities in Quality Control are carried out as per laid down Standard Operating Procedures.
As a long term ethically binding policy, we target, and commit ourselves to only those products that meet international cGMP standards. We continuously strive to achieve customer satisfaction 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. We continuously review our various operations to make them more efficient, relevant with changing international scenario a d and environment friendly. We comply with all relevant statutory and regulatory requirements.
Providing training to our employees is a regular feature in our calendar that fosters team spirit in addition to inculcate them with recent innovations and advancements in the industry around the world.
We stringently adhere to implementing Quality Management Systems and are committed towards making continual improvements to the same.
