Drugs Drugs 1600 Questions Ask question Search Order By: ActiveClear Filter 0 Votes 1 Ans Visual and analytical verification after cleaning, is one exclusive to the other? 1.59K viewsDrugsPharmaceutical 0 Votes 1 Ans For a non-sterile API intended for use in a sterile drug product, what level of equipment sanitization and/or sterilization is expected and how verified? 1.74K viewsDrugsPharmaceutical 0 Votes 1 Ans Is cleaning validation expected to take place when the first batches are produced for commercial use (process validation), even when such batches are produced on a pilot or small scale? 1.58K viewsDrugsPharmaceutical 0 Votes 1 Ans Is cleaning qualification sufficient? Would cleaning validation be expected once the API manufacturing was commercial and not clinical? 1.61K viewsDrugsPharmaceutical 0 Votes 1 Ans Regarding use of equipment for pre-clinical and clinical, is it allowable to use the same equipment for both as long as all operations are conducted under Q7A and as long as the worse case scenario is considered for cleaning? 1.81K viewsDrugsPharmaceutical 0 Votes 1 Ans Is cleaning validation required before the API starting material? 1.44K viewsDrugsPharmaceutical 0 Votes 1 Ans What is the minimum adequate interval for monitoring a validated cleaning process? 1.46K viewsDrugsPharmaceutical 0 Votes 1 Ans After calibration and/or maintenance of a process unit, is it required to clean the unit before use for processing? 1.52K viewsDrugsPharmaceutical 0 Votes 1 Ans Vendors of new equipment often ship you a vessel that has been polished. Often they do not know the chemical constitutes of the polish or of the gases. Our approach to cleaning, in this case, is use of a non-polar solvent to remove organics followed by a polar solvent to remove inorganics. Is this acceptable? 1.57K viewsDrugsPharmaceutical 0 Votes 1 Ans Please elaborate the definition of dedicated equipment. Equipment used on a campaign during six months can be considered dedicated during this period. Does cleaning validation apply if change of product is forecasted? 1.80K viewsDrugsPharmaceutical 0 Votes 1 Ans Wherever possible, food grade lubricants and oils should be used. Does that mean it’s okay to get into the batch? 1.94K viewsDrugsPharmaceutical 0 Votes 1 Ans What do you recommend in terms of status indicators for production equipment? 1.81K viewsDrugsPharmaceutical 0 Votes 1 Ans What was EWG’s thinking along the lines of consumable items such as inline filters, O – rings and gaskets? Is there an expectation that they are treated as job aids or equipment? 1.73K viewsDrugsPharmaceutical 0 Votes 1 Ans Is the performance of preventive maintenance required for each piece of GMP equipment? 1.57K viewsDrugsPharmaceutical 0 Votes 1 Ans Under preventive maintenance, is it acceptable to let certain equipment to go to failure, such as piping, manual valves, etc? 1.86K viewsDrugsPharmaceutical 0 Votes 1 Ans Are flexible hoses that are repeatedly used considered major equipment, therefore requiring maintenance? 1.39K viewsDrugsPharmaceutical 0 Votes 1 Ans Does Q7A provide for the matrix approach to equipment cleaning validation, or are companies expected to perform a separate cleaning validation for each compound? 1.37K viewsDrugsPharmaceutical 0 Votes 1 Ans Is it expected to establish a maximum time elapsed from the end of processing to cleaning? 1.59K viewsDrugsPharmaceutical 0 Votes 1 Ans Is there an expectation to establish time limits for clean equipment before that equipment needs to be recleaned? 1.71K viewsDrugsPharmaceutical 0 Votes 1 Ans Cleaning methods – are you looking for the active ingredient, the raw material, and byproduct in the cleaning methods? 1.58K viewsDrugsPharmaceutical « Previous 1 2 … 6 7 8 9 10 … 79 80 Next » Question and answer is powered by anspress.net
