Pharmaceutical Pharmaceutical 1645 Questions Ask question Search Order By: ActiveClear Filter 0 Votes 1 Ans Section 9.3 states that an example of a printed label needs to be included in the BPR. Does this requirement apply to hand printed labels? 1.13K viewsDrugsPharmaceutical 0 Votes 1 Ans You mentioned that name and manufacturer and address must be on the label. Would the name and address and the distributor be acceptable? 1.31K viewsDrugsPharmaceutical 0 Votes 1 Ans Someone stated that the quality unit must inspect packaging materials. Can that be delegated? 1.33K viewsDrugsPharmaceutical 0 Votes 1 Ans API labeling. For APIs manufactured, pre-validation for clinical products, is it required to include a statement limited for investigational use like what’s required for clinical products? 1.06K viewsDrugsPharmaceutical 0 Votes 1 Ans Labeling requirements in Section 9 seem excessively complicated where one batch of API requires label performed every few months. Can this system be simplified, i.e., fill in the blank labels? So they must be talking about product for clinicals. 1.19K viewsDrugsPharmaceutical 0 Votes 1 Ans Why do you have to take all markings off a container that you might reuse? 1.13K viewsDrugsPharmaceutical 0 Votes 1 Ans This has to do with inspection of packaging and labeling facilities for APIs. Is this intended to be the same level as for drug product line clearance? Can production personnel carry out this check, and does the requirement apply to API only or also to isolated intermediates? 1.15K viewsDrugsPharmaceutical 0 Votes 1 Ans Final product APIs – if the impurity profile changes as a result of scaling up, but still falls within required specifications, what is the status for this API? 1.08K viewsDrugsPharmaceutical 0 Votes 1 Ans Please explain the difference between specification and action limit. If there are no differences, why are both terms used? 1.09K viewsDrugsPharmaceutical 0 Votes 1 Ans For an API intended for a parenteral drug product that is lyophilized, is it sufficient to test the API powder for moisture content? Do microbiology/sterility issues need to be addressed? 1.15K viewsDrugsPharmaceutical 0 Votes 1 Ans For starting materials that have no pharmacopoeia monograph, are test methods required to be formally validated or can methods be justified on the basis of scientific logic? 986 viewsDrugsPharmaceutical 0 Votes 1 Ans Whose responsibility is it to obtain the stability information for a filing, i.e. IND, NDA, ANDA, the API manufacturer or the dosage form manufacturer? Does Q7A take a position on this? 1.23K viewsDrugsPharmaceutical 0 Votes 1 Ans If material is being shipped, can the retest date be on another document that is shipped with the material instead of the C-of-A or label? 1.28K viewsDrugsPharmaceutical 0 Votes 1 Ans Slide 11-11 indicates that a formal testing program is not needed to establish “use by”dates. Does this mean that the lab does not need to establish limits by a formal program for reference standard solutions or HPLC testing, where the standard solution is not prepared fresh each time? 930 viewsDrugsPharmaceutical 0 Votes 1 Ans Are formal stability studies required for an Intermediate that you are planning on holding? 1.19K viewsDrugsPharmaceutical 0 Votes 1 Ans If storage conditions are not defined on the label, what is the assumed ambient temperature? What is ambient temperature? How is it defined since it varies by geography and times of the year? 1.28K viewsDrugsPharmaceutical 0 Votes 1 Ans Is there going to be an attempt to harmonize water monographs in the future? 1.34K viewsDrugsPharmaceutical 0 Votes 1 Ans What does another unit exactly mean in the distribution procedure? 10.2? 1.21K viewsDrugsPharmaceutical 0 Votes 1 Ans Is it acceptable to store equipment cleaning logs and use logs in a single location such as a supervisor’s office rather than in close proximity to the corresponding equipment? 1.18K viewsDrugsPharmaceutical 0 Votes 1 Ans Q7A Section 9.4 makes a “requirement to use tamper evident packaging for shipments outside the company control”. True or false? 1.15K viewsDrugsPharmaceutical « Previous 1 2 … 48 49 50 51 52 … 82 83 Next » Question and answer is powered by anspress.net
