Pharmaceutical Pharmaceutical 1645 Questions Ask question Search Order By: ActiveClear Filter 0 Votes 1 Ans What is considered an adequate sample when tank loads of a raw material is received? 1.14K viewsDrugsPharmaceutical 0 Votes 1 Ans A pressurized tanker of hydrocarbon raw materials (isobutane, propane, etc.) is normally sampled and approved before pumping. What is the current Inspectorate policy for sample retention given the inherent risks generated by these flammable gases under pressure? 1.25K viewsDrugsPharmaceutical 0 Votes 1 Ans If a product is fabricated in Canada and exported outside of Canada (the product is not sold on the Canadian market), are samples of this finished product to be retained in Canada? 1.11K viewsDrugsPharmaceutical 0 Votes 1 Ans Do batches have to be tested for preservatives at initial release and then in the continuing stability program? 827 viewsDrugsPharmaceutical 0 Votes 1 Ans Can it be assumed that United States Pharmacopoeia (USP) chromatographic assay methods are stability indicating? 953 viewsDrugsPharmaceutical 0 Votes 1 Ans Is it acceptable to place an expiry date on a bottle cap instead of on the bottle label? 1.19K viewsDrugsPharmaceutical 0 Votes 1 Ans When the labelled expiration date states only the month and year does it mean the end of the month? 1.11K viewsDrugsPharmaceutical 0 Votes 1 Ans Can accelerated stability data of less than three months be used? 1.01K viewsDrugsPharmaceutical 0 Votes 1 Ans Should drugs packaged into kits and subsequently sterilized, be tested for stability? 1.16K viewsDrugsPharmaceutical 0 Votes 1 Ans Does the supervisor of a sterile product manufacturing facility need to have a degree in microbiology? 1.02K viewsDrugsPharmaceutical 0 Votes 1 Ans Should compendial test methods be validated? 1.11K viewsDrugsPharmaceutical 0 Votes 1 Ans Must all identification tests stated in a compendial monograph be performed? 1.21K viewsDrugsPharmaceutical 0 Votes 1 Ans Are solid dosage drugs exempted from dissolution testing if sold under a manufacturer’s standard? 775 viewsDrugsPharmaceutical 0 Votes 1 Ans Do products labelled as United States Pharmacopoeia (USP) have to be tested as per the USP test methods? 1.03K viewsDrugsPharmaceutical 0 Votes 1 Ans What should be the calibration frequency for a dissolution apparatus used with both baskets & paddles? 1.28K viewsDrugsPharmaceutical 0 Votes 1 Ans In performing system suitability as per United States Pharmacopoeia (USP) <621>, do all replicate injections have to be completed before any analyte sample injections are made? 860 viewsDrugsPharmaceutical 0 Votes 1 Ans Is routine product pH testing required for endotoxin (limulus amebocyte lysate – LAL) testing? 1.02K viewsDrugsPharmaceutical 0 Votes 1 Ans Is the use of recycled solvents for high performance liquid chromatography (HPLC) columns acceptable? 1.17K viewsDrugsPharmaceutical 0 Votes 1 Ans If one lot of a product made in a Mutual Recognition Agreement (MRA) country is split into two separate shipments, is it mandatory for the importer to obtain separate manufacturer’s batch certificate for each shipment? 1.05K viewsDrugsPharmaceutical 0 Votes 1 Ans Is it acceptable to perform the testing, including the potency, before packaging or is it mandatory to perform this testing after packaging? 1.21K viewsDrugsPharmaceutical « Previous 1 2 … 38 39 40 41 42 … 82 83 Next » Question and answer is powered by anspress.net
