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Get all SOPs of these all departments. Calibration and operating procedures of all quality control instruments and operating procedures of all production equipment are also provided on the website. All GMP topics are also covered for quality assurance."},"link":[{"rel":"http://schemas.google.com/g/2005#feed","type":"application/atom+xml","href":"https:\/\/www.pharmaguideline.com\/feeds\/posts\/default"},{"rel":"self","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/-\/GMP?alt=json-in-script\u0026max-results=5"},{"rel":"alternate","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/search\/label\/GMP"},{"rel":"hub","href":"http://pubsubhubbub.appspot.com/"},{"rel":"next","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/-\/GMP\/-\/GMP?alt=json-in-script\u0026start-index=6\u0026max-results=5"}],"author":[{"name":{"$t":"Ankur Choudhary"},"uri":{"$t":"http:\/\/www.blogger.com\/profile\/13017110634151977121"},"email":{"$t":"noreply@blogger.com"},"gd$image":{"rel":"http://schemas.google.com/g/2005#thumbnail","width":"31","height":"32","src":"\/\/blogger.googleusercontent.com\/img\/b\/R29vZ2xl\/AVvXsEgNClN3RTa7EsnxCU-cdUVaGyvB6DpC1Q4P9TZcFmSeaEKDDoxxY19aCofuB_T9QotdwXw5IuPkdx2-z-kmRgFaR5q6FFCuizQ5XlYe4No2v1X7rIaM37DnG4EQHiJ2FQ\/s220\/ankur-img.jpg"}}],"generator":{"version":"7.00","uri":"http://www.blogger.com","$t":"Blogger"},"openSearch$totalResults":{"$t":"268"},"openSearch$startIndex":{"$t":"1"},"openSearch$itemsPerPage":{"$t":"5"},"entry":[{"id":{"$t":"tag:blogger.com,1999:blog-2032508520370173515.post-4080435784701151080"},"published":{"$t":"2023-12-15T22:38:00.000+05:30"},"updated":{"$t":"2023-12-15T22:38:01.138+05:30"},"category":[{"scheme":"http://www.blogger.com/atom/ns#","term":"Audit"},{"scheme":"http://www.blogger.com/atom/ns#","term":"GDP"},{"scheme":"http://www.blogger.com/atom/ns#","term":"GMP"}],"title":{"type":"text","$t":"Determination of Data Integrity Compliance in Pharmaceuticals"},"content":{"type":"html","$t":"Data integrity is the principle of generating, maintaining and assuring the consistent accuracy and completeness of data in a company or manufacturing plant through the entire life cycle complying with the regulations set within the pharmaceutical industry by the Food and Drug Administration (FDA). \u003Ca href=\"https:\/\/www.pharmaguideline.com\/2018\/10\/data-integration-as-per-21-cfr-rules.html\" target=\"_blank\"\u003EData integrity\u003C\/a\u003E compliance is the key issue to be looked into especially in pharmaceuticals because this is the most sensitive sector dealing with individuals health.\u003Cbr\u003E\n\u003Ca href=\"https:\/\/www.pharmaguideline.com\/2019\/03\/determination-of-data-integrity-compliance.html#more\"\u003EContinue reading »\u003C\/a\u003E"},"link":[{"rel":"replies","type":"application/atom+xml","href":"https:\/\/www.pharmaguideline.com\/feeds\/4080435784701151080\/comments\/default","title":"Post Comments"},{"rel":"replies","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/2019\/03\/determination-of-data-integrity-compliance.html#comment-form","title":"0 Comments"},{"rel":"edit","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/4080435784701151080"},{"rel":"self","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/4080435784701151080"},{"rel":"alternate","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/2019\/03\/determination-of-data-integrity-compliance.html","title":"Determination of Data Integrity Compliance in Pharmaceuticals"}],"author":[{"name":{"$t":"Ankur Choudhary"},"uri":{"$t":"http:\/\/www.blogger.com\/profile\/13017110634151977121"},"email":{"$t":"noreply@blogger.com"},"gd$image":{"rel":"http://schemas.google.com/g/2005#thumbnail","width":"31","height":"32","src":"\/\/blogger.googleusercontent.com\/img\/b\/R29vZ2xl\/AVvXsEgNClN3RTa7EsnxCU-cdUVaGyvB6DpC1Q4P9TZcFmSeaEKDDoxxY19aCofuB_T9QotdwXw5IuPkdx2-z-kmRgFaR5q6FFCuizQ5XlYe4No2v1X7rIaM37DnG4EQHiJ2FQ\/s220\/ankur-img.jpg"}}],"media$thumbnail":{"xmlns$media":"http://search.yahoo.com/mrss/","url":"https:\/\/3.bp.blogspot.com\/-YHt2Uq0Kyw0\/XIU1gG-zAuI\/AAAAAAAAH7A\/ZHzIronVYs8fPi0lm2WUboSvziDCE4_ywCLcBGAs\/s72-c\/data-integrity-pharma.jpg","height":"72","width":"72"},"thr$total":{"$t":"0"}},{"id":{"$t":"tag:blogger.com,1999:blog-2032508520370173515.post-6172930915696648130"},"published":{"$t":"2023-12-14T23:16:00.000+05:30"},"updated":{"$t":"2023-12-14T23:16:50.717+05:30"},"category":[{"scheme":"http://www.blogger.com/atom/ns#","term":"Audit"},{"scheme":"http://www.blogger.com/atom/ns#","term":"GLP"},{"scheme":"http://www.blogger.com/atom/ns#","term":"GMP"}],"title":{"type":"text","$t":"6 Ways to Reduce Human Errors in Pharmaceuticals"},"content":{"type":"html","$t":"\u003Cdiv style=\"text-align: justify;\"\u003E\nHuman errors have critical effects on pharmaceutical product quality. About 80% of the product quality issues occur due to the human errors. Human errors are traced by the occurrence of the deviations in the process. Most of the root causes of deviations are human errors due to improper communication or failure to follow the written procedure.\u003C\/div\u003E\n\u003Ca href=\"https:\/\/www.pharmaguideline.com\/2016\/05\/6-ways-to-reduce-human-errors-in-pharmaceuticals.html#more\"\u003EContinue reading »\u003C\/a\u003E"},"link":[{"rel":"replies","type":"application/atom+xml","href":"https:\/\/www.pharmaguideline.com\/feeds\/6172930915696648130\/comments\/default","title":"Post Comments"},{"rel":"replies","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/2016\/05\/6-ways-to-reduce-human-errors-in-pharmaceuticals.html#comment-form","title":"1 Comments"},{"rel":"edit","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/6172930915696648130"},{"rel":"self","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/6172930915696648130"},{"rel":"alternate","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/2016\/05\/6-ways-to-reduce-human-errors-in-pharmaceuticals.html","title":"6 Ways to Reduce Human Errors in Pharmaceuticals"}],"author":[{"name":{"$t":"Ankur Choudhary"},"uri":{"$t":"http:\/\/www.blogger.com\/profile\/13017110634151977121"},"email":{"$t":"noreply@blogger.com"},"gd$image":{"rel":"http://schemas.google.com/g/2005#thumbnail","width":"31","height":"32","src":"\/\/blogger.googleusercontent.com\/img\/b\/R29vZ2xl\/AVvXsEgNClN3RTa7EsnxCU-cdUVaGyvB6DpC1Q4P9TZcFmSeaEKDDoxxY19aCofuB_T9QotdwXw5IuPkdx2-z-kmRgFaR5q6FFCuizQ5XlYe4No2v1X7rIaM37DnG4EQHiJ2FQ\/s220\/ankur-img.jpg"}}],"media$thumbnail":{"xmlns$media":"http://search.yahoo.com/mrss/","url":"https:\/\/1.bp.blogspot.com\/-D63Nvf4XbY0\/V0svB5q65pI\/AAAAAAAAFZg\/3gU1nA-Bzbw078RSVofxF-yMyXhBYCgTACLcB\/s72-c\/human-error.jpg","height":"72","width":"72"},"thr$total":{"$t":"1"}},{"id":{"$t":"tag:blogger.com,1999:blog-2032508520370173515.post-840209835181569809"},"published":{"$t":"2023-12-13T23:08:00.001+05:30"},"updated":{"$t":"2023-12-13T23:08:08.742+05:30"},"category":[{"scheme":"http://www.blogger.com/atom/ns#","term":"Audit"},{"scheme":"http://www.blogger.com/atom/ns#","term":"GDP"},{"scheme":"http://www.blogger.com/atom/ns#","term":"GMP"}],"title":{"type":"text","$t":"Key Preposes of Change Control in Pharmaceuticals"},"content":{"type":"html","$t":"Change control is an important part of the pharmaceutical \u003Ca href=\"https:\/\/www.pharmaguideline.com\/2016\/10\/quality-management-system-qms.html\" target=\"_blank\"\u003Equality management system\u003C\/a\u003E. It ensures that all changes are done in a controlled manner and changes made in the system do not have any adverse impact on the product quality. In this article, we will discuss the main purpose of the change control in pharmaceuticals.\u003Cspan\u003E\u003C\/span\u003E\u003Ca href=\"https:\/\/www.pharmaguideline.com\/2023\/12\/prepose-of-change-control.html#more\"\u003EContinue reading »\u003C\/a\u003E"},"link":[{"rel":"replies","type":"application/atom+xml","href":"https:\/\/www.pharmaguideline.com\/feeds\/840209835181569809\/comments\/default","title":"Post Comments"},{"rel":"replies","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/2023\/12\/prepose-of-change-control.html#comment-form","title":"0 Comments"},{"rel":"edit","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/840209835181569809"},{"rel":"self","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/840209835181569809"},{"rel":"alternate","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/2023\/12\/prepose-of-change-control.html","title":"Key Preposes of Change Control in Pharmaceuticals"}],"author":[{"name":{"$t":"Ankur Choudhary"},"uri":{"$t":"http:\/\/www.blogger.com\/profile\/13017110634151977121"},"email":{"$t":"noreply@blogger.com"},"gd$image":{"rel":"http://schemas.google.com/g/2005#thumbnail","width":"31","height":"32","src":"\/\/blogger.googleusercontent.com\/img\/b\/R29vZ2xl\/AVvXsEgNClN3RTa7EsnxCU-cdUVaGyvB6DpC1Q4P9TZcFmSeaEKDDoxxY19aCofuB_T9QotdwXw5IuPkdx2-z-kmRgFaR5q6FFCuizQ5XlYe4No2v1X7rIaM37DnG4EQHiJ2FQ\/s220\/ankur-img.jpg"}}],"media$thumbnail":{"xmlns$media":"http://search.yahoo.com/mrss/","url":"https:\/\/blogger.googleusercontent.com\/img\/b\/R29vZ2xl\/AVvXsEgIG0I71DzbjPfpOdQQkBCEi-g7yLJUc7Loy_skZZJlFBnKkPpTFIBGbfev_JKPcpeC7xnWiAPNFmkZSpGNAi5DjqrNlvUs1FUDb2I_X5Zvv3SYEqWc8PIdgO9yk8MI5BZooR_Rn7KH0LpcIkwT_GY-QtHxiIHoFD0cN6GCK0-8fooixvFLGHWjNlYBR_tu\/s72-w320-h260-c\/change-control.png","height":"72","width":"72"},"thr$total":{"$t":"0"}},{"id":{"$t":"tag:blogger.com,1999:blog-2032508520370173515.post-66120117584555901"},"published":{"$t":"2023-12-12T21:10:00.000+05:30"},"updated":{"$t":"2023-12-12T21:10:02.562+05:30"},"category":[{"scheme":"http://www.blogger.com/atom/ns#","term":"Audit"},{"scheme":"http://www.blogger.com/atom/ns#","term":"GMP"}],"title":{"type":"text","$t":"How to respond to an FDA 483 observations?"},"content":{"type":"html","$t":"FDA 483s are the observations found during the inspection of a pharmaceutical manufacturing facility. These observations are documented on a form known as form 483. After getting a notice from FDA on form 483 manufacturing facility has to respond to FDA about the actions taken on the observations. It is not a difficult task to respond to FDA if you have a plan.\u003Cspan\u003E\u003C\/span\u003E\u003Ca href=\"https:\/\/www.pharmaguideline.com\/2023\/03\/how-to-respond-to-fda-483-observations.html#more\"\u003EContinue reading »\u003C\/a\u003E"},"link":[{"rel":"replies","type":"application/atom+xml","href":"https:\/\/www.pharmaguideline.com\/feeds\/66120117584555901\/comments\/default","title":"Post Comments"},{"rel":"replies","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/2023\/03\/how-to-respond-to-fda-483-observations.html#comment-form","title":"0 Comments"},{"rel":"edit","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/66120117584555901"},{"rel":"self","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/66120117584555901"},{"rel":"alternate","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/2023\/03\/how-to-respond-to-fda-483-observations.html","title":"How to respond to an FDA 483 observations?"}],"author":[{"name":{"$t":"Ankur Choudhary"},"uri":{"$t":"http:\/\/www.blogger.com\/profile\/13017110634151977121"},"email":{"$t":"noreply@blogger.com"},"gd$image":{"rel":"http://schemas.google.com/g/2005#thumbnail","width":"31","height":"32","src":"\/\/blogger.googleusercontent.com\/img\/b\/R29vZ2xl\/AVvXsEgNClN3RTa7EsnxCU-cdUVaGyvB6DpC1Q4P9TZcFmSeaEKDDoxxY19aCofuB_T9QotdwXw5IuPkdx2-z-kmRgFaR5q6FFCuizQ5XlYe4No2v1X7rIaM37DnG4EQHiJ2FQ\/s220\/ankur-img.jpg"}}],"media$thumbnail":{"xmlns$media":"http://search.yahoo.com/mrss/","url":"https:\/\/blogger.googleusercontent.com\/img\/b\/R29vZ2xl\/AVvXsEg1JEt0-6ed5csY-aYw_xQsCeO8NJgZPaLgANUTSRuhl2kScPCjVdQ6K93OnSeIhamtubabrPH_mkJ7Mx1EFFBJA0Yzk8U-Vp2xzNQoprEUw4M28g06H4nJdX7SSME_gvmsh7g2tfZ1hpqN9ymw0LwjEwQBNLsYVyl5PauaoRnbE8otBL2gOySJ7XzJCg\/s72-w320-h247-c\/483-observations.png","height":"72","width":"72"},"thr$total":{"$t":"0"}},{"id":{"$t":"tag:blogger.com,1999:blog-2032508520370173515.post-2102017817771318789"},"published":{"$t":"2023-12-10T22:49:00.000+05:30"},"updated":{"$t":"2023-12-10T22:49:06.471+05:30"},"category":[{"scheme":"http://www.blogger.com/atom/ns#","term":"GDP"},{"scheme":"http://www.blogger.com/atom/ns#","term":"GMP"},{"scheme":"http://www.blogger.com/atom/ns#","term":"Quality Assurance"}],"title":{"type":"text","$t":"Different Types of Deviations in Pharmaceuticals"},"content":{"type":"html","$t":"Deviation management is an important part of pharmaceutical documentation. A lot of FDA warning letters are issued due to the improper handling of the deviations. Deviations are the departure of any process or procedure from a documented or expected value. \u003Ca href=\"https:\/\/www.pharmaguideline.com\/2011\/01\/deviation-control.html\" target=\"_blank\"\u003EDeviation\u003C\/a\u003E may be in the form of value, process, or procedure that is different from the standard or guideline.\u003Cspan\u003E\u003C\/span\u003E\u003Ca href=\"https:\/\/www.pharmaguideline.com\/2023\/12\/different-types-of-deviations.html#more\"\u003EContinue reading »\u003C\/a\u003E"},"link":[{"rel":"replies","type":"application/atom+xml","href":"https:\/\/www.pharmaguideline.com\/feeds\/2102017817771318789\/comments\/default","title":"Post Comments"},{"rel":"replies","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/2023\/12\/different-types-of-deviations.html#comment-form","title":"0 Comments"},{"rel":"edit","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/2102017817771318789"},{"rel":"self","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/2102017817771318789"},{"rel":"alternate","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/2023\/12\/different-types-of-deviations.html","title":"Different Types of Deviations in Pharmaceuticals"}],"author":[{"name":{"$t":"Ankur Choudhary"},"uri":{"$t":"http:\/\/www.blogger.com\/profile\/13017110634151977121"},"email":{"$t":"noreply@blogger.com"},"gd$image":{"rel":"http://schemas.google.com/g/2005#thumbnail","width":"31","height":"32","src":"\/\/blogger.googleusercontent.com\/img\/b\/R29vZ2xl\/AVvXsEgNClN3RTa7EsnxCU-cdUVaGyvB6DpC1Q4P9TZcFmSeaEKDDoxxY19aCofuB_T9QotdwXw5IuPkdx2-z-kmRgFaR5q6FFCuizQ5XlYe4No2v1X7rIaM37DnG4EQHiJ2FQ\/s220\/ankur-img.jpg"}}],"media$thumbnail":{"xmlns$media":"http://search.yahoo.com/mrss/","url":"https:\/\/blogger.googleusercontent.com\/img\/b\/R29vZ2xl\/AVvXsEgsmu7DNl-phPWq9TOcZTfGaRIqw8B7qnQ49kPv24VUudPoR6yirkdcPkLR-9uoxFrbRb1Vu68ZDQGYZzcu_Jxp0w2VhHYKYfNLwPeIc5Qs_IP3-Nj3k6rT7ie6YSKtM6vVU2ZlAm5r5YZ0By5zlo79I3xt8Yecpz4TgZnfzDFfuthY5-w-Kxm-fBbIc7Nv\/s72-c\/deviation.jpeg","height":"72","width":"72"},"thr$total":{"$t":"0"}}]}});