Questions Ask question Search Order By: ActiveCategoryClear Filter 0 Votes 1 Ans What happens after FDA notifies a food facility that FDA intends to inspect their facilities? 1.75K viewsFood Safety 0 Votes 1 Ans Is a FDA food inspection the same as a food safety system’s audit? 1.43K viewsFood Safety 0 Votes 1 Ans What systems does FDA have in place to protect the U.S. food supply? 1.67K viewsFood Safety 0 Votes 1 Ans What is FDA doing to ensure the safety of products imported from Japan? 1.59K viewsFood Safety 0 Votes 1 Ans What specific tests is FDA using? 1.45K viewsFood Safety 0 Votes 1 Ans What does FDA look for when it test food for radioactive contamination? 1.62K viewsFood Safety 0 Votes 1 Ans What are the standards FDA uses to determine the amounts of specific radioactive materials in foods and whether they may cause a safety concern? 1.61K viewsFood Safety 0 Votes 1 Ans What businesses must comply with HIPAA laws? 1.68K viewsHIPAAHospital and Healthcare 0 Votes 1 Ans What is Protected Health Information (PHI)? 1.52K viewsHospital and Healthcare 0 Votes 1 Ans Will a laboratory subsequently be notified of GLP deviations not listed on the FDA-483? 1.45K viewsFDA 0 Votes 1 Ans What amount of detail should be included in the standard operating procedures (SOPs)? 1.41K viewsFDA 0 Votes 1 Ans To what extent are computer programs to be documented as SOPS? 1.44K viewsFDA 0 Votes 1 Ans Regarding computer validation, is it necessary to second check all data into the computer system or only the critical data? 1.41K viewsFDA 0 Votes 1 Ans Revalidation of computerized systems. What is required for computerized materials management systems used to monitor receipts, sampling testing or release of materials? 1.71K viewsFDA 0 Votes 1 Ans When making corrections to documented entries, the only requirements are to sign, date, and leave original entry readable. Was there any discussion when writing Q7A to also record the reason for the change? Will field investigators expect this? 1.68K viewsFDA 0 Votes 1 Ans Please expand on what is acceptable as true copies. Do you mean actual reproductions in place of originals, scanned records, or validated computer system accepted by the FDA? 1.27K viewsFDA 0 Votes 1 Ans Is there a distinction between a significant and a critical step? Q7A does not define “significant”? 1.53K viewsFDA 0 Votes 1 Ans How does the FDA plan to determine how much time should be required between the application of raw manure and the harvest of produce covered by the rule? 1.66K viewsFood Safety 0 Votes 1 Ans What were the primary findings of the Final Environmental Impact Statement (EIS) and Record of Decision (ROD)? 1.72K viewsFood Safety 0 Votes 1 Ans Why is FDA increasing surveillance of imported food products? 1.61K viewsFood Safety « Previous 1 2 … 45 46 47 48 49 … 283 284 Next » Question and answer is powered by anspress.net
