哪位英语高手帮忙翻译一下：一小段话

Collect, analyze the quality of information, to monitor the quality of dynamic handling and quality.
Learn about the product quality laws and regulations.The attention to quality control, scientific approach to development.
Quality management and quality standards for document preparation, revision and implementation.
Participate in the preparation and revision of documents and document management.
Involved in the entire process of product quality for effective monitoring.
According to the "standard" requirement for the development of quality assurance system, organization and implementation and undertake the following duties :
Formulation and revision of the internal control standards and testing of materials and products practices;
Develop sampling and sample keeping system.
Formulated using test equipment, apparatus, reagents, test solution, the test drug, standard (or tablet), titrant,management approach and the implementation of the medium.
Decide whether or not to use materials and intermediate products.
Production records for audit.Audit includes batching, weighing the review process, the various manufacturing processes and inspection records-records,semi-quality test results, the error handling, product test results.Meet the requirements and audit staff products can only be released after the signing.
Unqualified audit and Inspection Service in quality management responsibilities.
Responsible for the quality of the paper document management.
Responsible for the supervision and control of the entire process.
Responsible for product quality and consumer complaints on the treatment and recovery of goods, products supervision of the destruction.
Responsible for the monitoring and reporting of adverse drug reactions.
GMP self-handling procedures involved.