Quality assurance in the pharmaceutical industry

Pharmaceutical quality assurance is a dynamic process, a State of mind or an understanding of the guidelines on the development and manufacture of pharmaceutical products and.
Quality assurance a part of quality management is riveted to assure accurate and reliable results, all generate practical exercises are carried out. Drugs that are placed on the market must be safe and therapeutically active. Performance should be consistent and predictable. Or it can be defined as the sum of all activities and responsibilities required to ensure that the drug, the patient reaches is safe and effective.
The system of quality assurance
This Department is divided into four main areas: quality control, production, distribution and inspection.
1. QA ensures the arrangements for the production, distribution and application of correct from and packaging.
(2) Any deviation from the written production and process control examines procedures are followed in the execution of various production and process control functions to be listed and recorded by the quality Department
3. Deviations from the established deadlines for the completion of each stage of production are established and documented by the Dept. d'Assurance
4. All activities involved in the manufacturing process, in process control and bulk tests shall be approved by the QA department
5. All necessary control on intermediate products and other in-process controls and validations are carried out by the Department
6. Quality improvement plans.
7. Validation and technology transfer.
8. Review of the stability date and durability of the products.
9. Quality team often conduct GMP training for staff at all levels of the organization.
Quality assurance goals
1 Make sure that a patient achieve secure any medicine, is effective and the standard quality.
2 About drugs that are safe and effective.
Use superiority of a product of selection 3 back up.
4 Persistent products are safely and effectively structured selection and procurement methods.
5 Exerting products through appropriate storage, distribution and use methods.
Conclusion
Quality assurance does his best to maintain the reliability in every phase of the manufacturing process from research, clinical trials, quality control, production, distribution and informs about fair use, and analyzes security and details of the products.
The Department helps in the strategic direction and development of quality systems, standard operating procedures, and document programs to ensure corporate policies and regulatory requirements.
It is a multi fold activity where in all industries want to professionally qualified, competent, experienced management and entrepreneurial talent workers, the industry lead.