Pharmaceutical Pharmaceutical 1645 Questions Ask question Search Order By: ActiveClear Filter 0 Votes 1 Ans Cleaning records, maintenance records don’t appear to have to be reviewed or checked anymore by a second person or supervisor. Is this true? 1.39K viewsDrugsPharmaceutical 0 Votes 1 Ans Review of critical process steps. Is the complete review of the batch record for a critical process step, meaning a synthetic step, or is it a review of the critical variables within the critical step? 1.70K viewsDrugsPharmaceutical 0 Votes 1 Ans Will API firms be held accountable to these guidelines even though operations were conducted prior to effective date of Q7A? 1.82K viewsDrugsPharmaceutical 0 Votes 1 Ans In which document does one designate the API starting material, the drug master file or some other filing application? 1.74K viewsDrugsPharmaceutical 0 Votes 1 Ans Is it necessary to complete any investigations including out of specification investigations (OOS), prior to release of product? 1.80K viewsDrugsPharmaceutical 0 Votes 1 Ans What types of controls are expected if the calibration of equipment is contracted to outside agencies? 1.82K viewsDrugsPharmaceutical 0 Votes 1 Ans Master batch instructions written by a word processor using something like Microsoft Word, then printed, reviewed and approved as a hard copy, which is signed and dated. True or false, is this an electronic record? 1.80K viewsDrugsPharmaceutical 0 Votes 1 Ans Section 4.2 requires utility system drawings be available. What level of documentation/drawings is expected? Are piping and instrumentation diagrams sufficient, or are drawings showing actual dimensions expected? 1.55K viewsDrugsPharmaceutical 0 Votes 1 Ans The CGMP regulations for drug products, 21 CFR 211, specify a written record of major equipment cleaning, maintenance, and use shall be included in the individual equipment logs. Q7A does not specify individual equipment logs, only records. Does this mean individual equipment logs are no longer necessary/ expected for API manufacturing? 1.46K viewsDrugsPharmaceutical 0 Votes 1 Ans What microbial controls is the manufacturer required to have in place for an API used in clinical trials for parenteral drug product even if the manufacturer has no responsibility for the end use of the API? 1.65K viewsDrugsPharmaceutical 0 Votes 1 Ans Does the list of raw materials need to include a list of filters and other commodities? Does Q7A require control of durables and consumables? 1.77K viewsDrugsPharmaceutical 0 Votes 1 Ans Is there a list or reference available that defines objectionable organism? 1.86K viewsDrugsPharmaceutical 0 Votes 1 Ans Why was the validation protocol not used as a source document for defining critical parameters? 1.83K viewsDrugsPharmaceutical 0 Votes 1 Ans What degree of validation should be necessary when data is recorded on a computer and a second system, i.e. paper batch record? Differences could exist in the degree of accuracy on the computer versus the paper. Also, in deciding if a deviation is critical, would one normally expect to see what requirements are critical versus non-critical predefined in the production instructions? If not, what justification would you expect to see? 1.85K viewsDrugsPharmaceutical 0 Votes 1 Ans Section 6.5 says, “. . . should include complete information relating to production,” yet clarification to 6.3 says “. . . short document for recording results;” please explain the discrepancy. 1.53K viewsDrugsPharmaceutical 0 Votes 1 Ans What is the group’s opinion of detergent cleaning versus solvent cleaning? 1.69K viewsDrugsPharmaceutical 0 Votes 1 Ans Solvents used for cleaning equipment. May these be recovered? 1.86K viewsDrugsPharmaceutical 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? 1.66K 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? 1.77K viewsDrugsPharmaceutical « Previous 1 2 … 72 73 74 75 76 … 82 83 Next » Question and answer is powered by anspress.net
