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? 1.31K 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? 1.43K 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? 1.27K viewsDrugsPharmaceutical 0 Votes 1 Ans Do batches have to be tested for preservatives at initial release and then in the continuing stability program? 995 viewsDrugsPharmaceutical 0 Votes 1 Ans Can it be assumed that United States Pharmacopoeia (USP) chromatographic assay methods are stability indicating? 1.11K viewsDrugsPharmaceutical 0 Votes 1 Ans Is it acceptable to place an expiry date on a bottle cap instead of on the bottle label? 1.34K viewsDrugsPharmaceutical 0 Votes 1 Ans When the labelled expiration date states only the month and year does it mean the end of the month? 1.54K viewsDrugsPharmaceutical 0 Votes 1 Ans Can accelerated stability data of less than three months be used? 1.16K viewsDrugsPharmaceutical 0 Votes 1 Ans Should drugs packaged into kits and subsequently sterilized, be tested for stability? 1.32K viewsDrugsPharmaceutical 0 Votes 1 Ans Does the supervisor of a sterile product manufacturing facility need to have a degree in microbiology? 1.19K viewsDrugsPharmaceutical 0 Votes 1 Ans Should compendial test methods be validated? 1.27K viewsDrugsPharmaceutical 0 Votes 1 Ans Must all identification tests stated in a compendial monograph be performed? 1.37K viewsDrugsPharmaceutical 0 Votes 1 Ans Are solid dosage drugs exempted from dissolution testing if sold under a manufacturer’s standard? 959 viewsDrugsPharmaceutical 0 Votes 1 Ans Do products labelled as United States Pharmacopoeia (USP) have to be tested as per the USP test methods? 1.20K viewsDrugsPharmaceutical 0 Votes 1 Ans What should be the calibration frequency for a dissolution apparatus used with both baskets & paddles? 1.49K 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? 1.04K viewsDrugsPharmaceutical 0 Votes 1 Ans Is routine product pH testing required for endotoxin (limulus amebocyte lysate – LAL) testing? 1.18K viewsDrugsPharmaceutical 0 Votes 1 Ans Is the use of recycled solvents for high performance liquid chromatography (HPLC) columns acceptable? 1.34K 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? 1.21K 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? 1.37K viewsDrugsPharmaceutical « Previous 1 2 … 38 39 40 41 42 … 82 83 Next » Question and answer is powered by anspress.net
