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Zhenyuan Pharm has improved quality standards, set up
a full set of Standard Operation Process (SOP) and Standard
Management Process (SMP) with periodical rechecks and
amendments according to the requirements of GMP. For example,
Zhenyuan Pharm has set up an experimental process for
products stability and Good Laboratory Practice (GLP),
which ensures products safe and effective within the valid
period and also ensure experimental data accurate and
reliable. Zhenyuan Pharm now has finished DMF materials
for the US or European GMP inspection of its main bulk
drugs such as Nystatin, Roxithromycin, Netilmicin, Cefetamet
pivoxil hydrochloride etc. Now it is in the process of
registration and authentication. The quality control department
and its central analytical laboratories have professional
technicians and advanced equipment. They are in charge
of materials purchasing, receiving, storing, and delivery,
strictly controlling the process of inspection, storing,
delivery and destroying of labels and package inserts
to ensure products safe and effective. |
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