Drugs Drugs 1600 Questions Ask question Search Order By: ActiveClear Filter 0 Votes 1 Ans At what stage of process development is the validation of viral clearance required? 1.30K viewsDrugsPharmaceutical 0 Votes 1 Ans For biotech cleaning validation, is it sufficient to validate the cleaning from rinse samples? What additional tests might be considered from swab samples? 1.34K viewsDrugsPharmaceutical 0 Votes 1 Ans What type of qualification would be expected for steam used to sterilize media in a classical fermentation process? 1.04K viewsDrugsPharmaceutical 0 Votes 1 Ans Representative intermediates or APIs can be used for cleaning validation: does this mean a placebo API might be substituted in the case of very high active or very high value protein production? And, what would be considered representative, only those properties that affect cleaning? 1.29K viewsDrugsPharmaceutical 0 Votes 1 Ans Is the expectation for process validation being completed before commercial distribution of the final drug the same for CDER and for CBER regulated products? 1.12K viewsDrugsPharmaceutical 0 Votes 1 Ans What are the expectations when validating the in situ sterilization of culture media in a fermentation process? Is this done in the traditional way when validating an autoclave, for instance using temperature monitoring with thermocouples and biological indicators, or can the sterilized broth be sampled and tested for sterility? 888 viewsDrugsPharmaceutical 0 Votes 1 Ans Should process validation be performed on classical fermentation? For classical fermentation, should the sterilization operation be validated? 1.12K viewsDrugsPharmaceutical 0 Votes 1 Ans In a classical fermentation, is it necessary to validate the process no matter if we consider the step a non-critical one? The other one is what guidance can you give for validation of classical fermentation processes? What type of factors should be considered for validation? 1.22K viewsDrugsPharmaceutical 0 Votes 1 Ans Would it be expected that the sterilization process of fermenters be validated for a classical fermentation operation? 1.16K viewsDrugsPharmaceutical 0 Votes 1 Ans In classical fermentation, history would be, the fermentation operation itself is obviously in a closed vessel and the environment around that vessel is non-controlled, quite frankly. I hear you saying, in the biotech area, or the cell culture area, that you’re suggesting or saying that you need at least a 100,000 classification. Can you explain to the people here as to why, number one, that has evolved, and two, are you suggesting that you need that kind of environment than classical fermentation too? 1.21K viewsDrugsPharmaceutical 0 Votes 1 Ans Please comment on the environmental monitoring and air space classification in facilities generating API from MMC (assuming that mammalian cell culture, and fermentation processes). There is a breadth of practice and inspectional findings in the industry. 1.36K viewsDrugsPharmaceutical 0 Votes 1 Ans How stringent must the environmental monitoring program be for the biotech API facility? Do you expect to see the same level of monitoring that is done in a filling facility? Is passive monitoring sufficient? 1.11K viewsDrugsPharmaceutical 0 Votes 1 Ans What type of controls/room classifications/gowning, etc., would you expect for a media prep area of a dedicated biotech facility, especially if the media raw materials have a known but unpredictable level of bioburden? 1.20K viewsDrugsPharmaceutical 0 Votes 1 Ans The integrity test on the final sterilizing filter for parental products is required to be implemented in situ. However, it is hard to do because they’re a big facility consisting of many cartridges. Is an off line test instead of an in situ test acceptable? 1.33K viewsDrugsPharmaceutical 0 Votes 1 Ans Can the product of a classical microbial fermentation be classified as a starting material in the preparation of an API? It kind of gets to both the small molecule as well as fermentation. 1.18K viewsDrugsPharmaceutical 0 Votes 1 Ans Is systemic autoclaving part of routing materials into a Class 100,000 facility? 1.38K viewsDrugsPharmaceutical 0 Votes 1 Ans In the case of mammalian cell culture where inherent viruses must be removed during purification, to what extent does the equipment suites, etc. need to be segregated? 984 viewsDrugsPharmaceutical 0 Votes 1 Ans For APIs that are small molecules, as long as your reactor is closed and what is outside the reactor does not really matter, what you really care about is what the API sees (if you pretend you are the API). With biological processes, it tends to be a little tighter specification, is that what you’re getting at? 1.33K viewsDrugsPharmaceutical 0 Votes 1 Ans Biotech API (manufacturing, fermentation, primary recovery, and purification) where closed unit operations are used could be manufactured in facilities with lower environmental classifications than many of the facilities currently found in the biotech industry. Many biotech API facilities with closed unit operations have been built to ensure drug product environmental standards. Comments? 1.15K viewsDrugsPharmaceutical 0 Votes 1 Ans Assuming quality systems are operational, please comment on the fate of product when PQ requires actual API processing. Can it be sold provided successful validation follows and specs are met? Examples would be chromatography and those types of steps. 1.32K viewsDrugsPharmaceutical « Previous 1 2 … 60 61 62 63 64 … 79 80 Next » Question and answer is powered by anspress.net
