The Quality Assurance Department ensures that products are produced and tested in accordance with GMP requirements.
Technology-driven
Promoting development with quality
Serving human health
Submit product registration application in CTD format
Respond to questions or defects from regulatory/customer
Submit an annual report to the regulatory body
Supplier audit and approval
Confirmation of facilities, equipment and analytical instruments
Verification of processes, methods, cleaning, etc.
Handling complaints, deviations, change control, product recalls
Handling the inspection of supervision department, customer audit
Establish and maintain a document system that meets regulatory requirements
Provide training for personnel
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