Drugs Drugs 1600 Questions Ask question Search Order By: ActiveClear Filter 0 Votes 1 Ans If a GLP inspector requests information retained in an archive, can a test facility respond by retrieving electronic records from a company’s global electronic archiving system (physically located in another country)? 1.48K viewsDrugsPharmaceutical 0 Votes 1 Ans Best method for designing a statistically sound sample plan for a pharmaceutical packaging process? – In the packaging process we are looking at several different attributes varying from critical defectives (AQL .065) to minor defectives (AQL 1.5). It is the goal to use one sample size that would statistically cover the different AQL range. If we have a batch size of 20,000 and a samples size of 315, would it be safe to say that the pass/reject level for AQL .065, 0-1 and 10-11 for an AQL 1.5. Is it statistically sound that we just pull one sample size? 1.31K viewsDrugsPharmaceutical 0 Votes 1 Ans ANDA OTC, prescription RLD NDA approved products – Can there be an ANDA OTC? 1.65K viewsDrugsPharmaceutical 0 Votes 1 Ans Monographed product changes reporting -How do you report changes if you have a monographed product? 1.66K viewsDrugsPharmaceutical 0 Votes 1 Ans OTC drug registration-U.S. agent requirements and responsibilities – In order to register an OTC drug in the U.S. does the U.S. agent have to physically live or operate a business in the U.S. or can this agent live elsewhere? 1.52K viewsDrugsPharmaceutical 0 Votes 1 Ans Post approval change requirements of monographed products 1.57K viewsDrugsPharmaceutical 0 Votes 1 Ans We are a start-up biotech company and need to set-up a raw materials testing program. Final product labels are our current priority. 1.33K viewsDrugsPharmaceutical 0 Votes 1 Ans What are the guidelines on correcting an entry or errors after an analysis or a process is complete? 1.60K viewsDrugsPharmaceutical 0 Votes 1 Ans When doing microbial counts, is using negative controls that succeed proof enough that testing is not the issue? 1.57K viewsDrugsPharmaceutical 0 Votes 1 Ans Do you recommend daily flushing of POU drops that are not routinely used? 1.62K viewsDrugsPharmaceutical 0 Votes 1 Ans Is there an ideal or recommended number of POU drops that are included in a distribution loop? 1.60K viewsDrugsPharmaceutical 0 Votes 1 Ans How often is sanitization of typically recommended? 1.48K viewsDrugsPharmaceutical 0 Votes 1 Ans If the WFI distribution system circulates at 85 degrees C , is sanitization required? 1.39K viewsDrugsPharmaceutical 0 Votes 1 Ans Do you recommend any special strategy for evaluating increasing the interval between routine sanitization for system that has been operating without issues? 1.39K viewsDrugsPharmaceutical 0 Votes 1 Ans Pharmaceutical water System Biofilm-Growth through Penetration – How quickly can 0.2 micron filters suffer from growth through penetration 1.71K viewsDrugsPharmaceutical 0 Votes 1 Ans What is the difference between retest date and expiration date for drug substances? 1.50K viewsDrugsPharmaceutical 0 Votes 1 Ans 1.Whether Study sample analysis will be conducted before long term stability completion.(Bio analytical) 2.Immediately after completion of validation,long term stability in Biological matrix is required? 1.65K viewsDrugsPharmaceutical 0 Votes 1 Ans If there is dead biofilm present in the water system, will this show itself with higher TOC counts? 1.60K viewsDrugsPharmaceutical 0 Votes 1 Ans Are you familiar with reports on aspergilli in hospital water systems? Any pertinence to Purified Water systems for pharma? 1.44K viewsDrugsPharmaceutical 0 Votes 1 Ans how capa helps pharmaceutical industry 1.57K viewsDrugsPharmaceutical « Previous 1 2 … 14 15 16 17 18 … 79 80 Next » Question and answer is powered by anspress.net
