Pharmaceutical Pharmaceutical 1645 Questions Ask question Search Order By: ActiveClear Filter 0 Votes 1 Ans Does each workflow on our computer system need to be validated? 1.26K viewsDrugsPharmaceutical 0 Votes 1 Ans How should we access to CGMP computer systems be restricted? 950 viewsDrugsPharmaceutical 0 Votes 1 Ans Why is FDA concerned with the use of shared login accounts for computer 198 systems? 1.19K viewsDrugsPharmaceutical 0 Votes 1 Ans How should blank forms be controlled? 1.26K viewsDrugsPharmaceutical 0 Votes 1 Ans How often should audit trails be reviewed? 1.15K viewsDrugsPharmaceutical 0 Votes 1 Ans Who should review audit trails? 1.29K viewsDrugsPharmaceutical 0 Votes 1 Ans Hello, is is useful to review the “windows eventviewer” for GxP devices? 1.22K viewsDrugsPharmaceutical 0 Votes 1 Ans Must the report for a riew of the audit trail be generated by the system itself? Or is it possible to use another system which is better suited for carrying out analyses? 1.12K viewsDrugsPharmaceutical 0 Votes 1 Ans I think, I did not express myself very clearly when asking the question: Is it only reviewed whether the process is still functioning in the course of the periodic reviews – hence, if the audit trail data is still recorded? Meaning: Functionality is documented by IT with a few samples. 1.26K viewsDrugsPharmaceutical 0 Votes 1 Ans May the Head of Laboratory have admin rights for example to carry out the audit trail review? 1.36K viewsDrugsPharmaceutical 0 Votes 1 Ans Is it possible for a user to have two system accounts? One as a user and one as administrator or reviewer? 1.24K viewsDrugsPharmaceutical 0 Votes 1 Ans Do you know a system that fulfils all requirements for the audit trail function of a CDS? 775 viewsDrugsPharmaceutical 0 Votes 1 Ans File based data retention: Deletion is possible outside the software. How is it possible to “build in” safety? 976 viewsDrugsPharmaceutical 0 Votes 1 Ans What are metadata? 1.01K viewsDrugsPharmaceutical 0 Votes 1 Ans Equipment often has a standard audit trail function. A lot of data is recorded (on/off), but only a small part of it is critical or relevant for a review. What is the best way to proceed when carrying out a review? 1.22K viewsDrugsPharmaceutical 0 Votes 1 Ans What is the way to proceed in the case of facilities in the production area such as AP production, mixers, filling lines with variable parameters as concerns classification of data/systems, extent and intervals of review? 1.11K viewsDrugsPharmaceutical 0 Votes 1 Ans Whose job is it to carry out the audit trial review in the laboratory? 1.30K viewsDrugsPharmaceutical 0 Votes 1 Ans Must all electronic data be stored and archived in the case of a process in the sterile area or is the batch record sufficient? 1.17K viewsDrugsPharmaceutical 0 Votes 1 Ans Would you consider changes of the parameters / formulations at production facilities as dynamic data? Do I have to consider them at every batch? 831 viewsDrugsPharmaceutical 0 Votes 1 Ans Are the analytical data arising in the course of the validation of analytical procedures critical data? 1.19K viewsDrugsPharmaceutical « Previous 1 2 … 30 31 32 33 34 … 82 83 Next » Question and answer is powered by anspress.net
