Test performed to compare the weight or volume of a product filled into each container with their labeled weight or volume(1 Point)Water contentMinimum fillStorageall of the thesenone of theseWhich is a common biological indicator for pharmaceutical sterilization processes?(1 Point)B. subtilisC. difficileC. albicansH. influenzaeRecommended packaging of ointments:(1 Point)Collapsible tubestight containerswell-closed containersall of the thesenone of theseWhich of the following types of inert ingredients/substances is prohibited in injections?(1 Point)AntioxidantspH buffersAntimicrobial preservativesColoringsBenzyl alcoholWhich is an advantage of suspensions over solutions for ophthalmic delivery?(1 Point)Suspensions do not cause stinging or burning sensation.Suspensions provide a longer corneal contact time.Suspensions do not require a preservative.One drop of suspension is smaller than one drop of solution.The eye can hold a greater volume of suspension than solution.Which of the following technologies is an example of reverse genetics?(1 Point)Recombinant DNAPolymerase chain reactionGene insertionMurine MAbAntisense RNA

Which of the following is not a requirement for the packaging of sterile injectable products? A. Single dose products must be packaged in vials or ampules that contain less than 30 ml. B. A single dose container must be hermetic but once it has been opened it cannot be resealed with assurance that sterility has been maintained. C. A multi-dose container must be hermetic, but due to the packaging, the sterility of the contents is maintained to allow withdrawal of successive doses. D. The material of the container and its closure must not interact with the drug preparation in a way that alters the strength or efficacy of the product.

USP requires tests for capsules that include which of the following? Stability testing, and disintegration testing Added substances and dissolution test Content uniformity and weight variation All of these are required tests so this is the answer

Describe a test to identify the gas used to sterilise water. [2 marks] Test Result

The dissolution of the drug from the dosage unit during the elapsed time is the USP test requirement for which of the following? A. Product uniformity and weight variation B. Drug release for extended release or delayed release dosage forms C. Microencapsulation and fluid bed processing D. Teeth, hair and eyeballs

How can XYZ company evaluate or validate the sterilization process for their new parenteral injectable product? A. run the sterilization process on product with an immunobiologic in it that is immune to the sterilization process B. put microbes into some containers of product, run the sterilization process then test the product for sterility C. run the sterilization on non-sterile product and then test for sterility D. run the sterilization with a biologic indicator in it