THE HALLMARK OF KRIVEN IS QUALITY
At Kriven Pharma we all are committed to supplying products of required quality with delivery schedules, in order to achieve theCustomer satisfaction. We ensure various resources and competency of our people and their proficiency in the related works to have continual improvement.
The Quality Assurance and Control Department is having well-qualified and experienced personnel, who are directly reporting to the Managing Director who is independent of production. All Personnel of QC has definite responsibilities.
All activities of QC are performed as per the standard operating procedures. Qualified personnel carry out analysis as per the SOP and as per customers' specifications and requirements. Quality is assured through a well-defined system, but not limited to viz., input control, in-process testing and finished goods analysis supported by proper documentation, qualified equipment, calibrated measuring and testing instruments and by imparting training of the personnel.
How does Kriven ensure utmost quality is being delivered to you?
- All the persons involved in the manufacturing, storage & distribution of the products are responsible for the Quality.
- All the activities of the site are as per the Quality plan.
- There is a Quality Unit that is independent of production and that fulfils Assurance and Control responsibilities and reports directly to the Managing Director.
- No materials are released or used before the satisfactory completion of evaluation by the quality unit unless there are appropriate systems in place to allow for such procedures.
- The persons authorised to release the finished products to market has been specified.
- All Quality related activities are recorded at the time they are performed.
- Procedures exist to regulate this process and to notify responsible management.
- Quality Assurance is involved in all quality-related matters.
- All the Department responsibilities are well defined and communicated.