Current Category: CN-YBB - Drug packaging
This method is applicable to the determination of stress in pharmaceutical glass containers.
This standard applies to composite rigid films made primarily from polyvinyl chloride (PVC), polyethylene (PE), and polyvinylidene chloride (PVDC), which are used for blister packaging of solid medicines (tablets, capsules, etc.)
This standard applies to low-borosilicate glass moulded injection bottles used for directly packaging injections, sterile powders for injection, and concentrated solutions for injection
This standard applies to plastic bottles for external use liquid preparations, which are mainly made of high-density polyethylene (HDPE) and produced by injection-blow molding process
This standard applies to sodium-calcium glass tubes used to package oral liquids, whether they have undergone neutralization treatment or not
This method is applicable to the determination of the puncture force of rubber stoppers and pads used in injections. The puncture force refers to the maximum force value required for the puncture instrument to penetrate the rubber stopper or pad during the puncture test, expressed in Newtons (N)
This method is applicable to the determination of residual monomer dichlorodifluoroethylene in polyvinyl chloride products
This standard applies to brominated butyl rubber pistons for pre-filled syringes. The piston types are either snap-fit (PSL) or threaded (PT).
This method is applicable to the determination of the heat-sealing strength of plastics welded to plastics or other substrates (such as aluminum foil, etc.) and the heat-sealing strength of plastic composite bags
This standard applies to low-borosilicate glass tubes used to package oral liquid medicines in oral liquid bottles
The compatibility test between drug packaging materials and drugs refers to a test conducted to investigate whether there are phenomena such as migration or adsorption between drug packaging materials and drugs, which may subsequently affect the quality of the drugs. Due to the numerous types of packaging materials, the diversity of packaging containers, and the differences in the formulations being packaged, this test is designed to be conducted in a convenient and effective manner, and these guidelines have been formulated specifically for this purpose.
This method is applicable to the determination of the vertical axis deviation of medicinal glass bottles with a circular shape and the roundness deviation of ampoules. This method is generally not used for shaped bottles (except for those with a fixed bottom axis line)