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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\/-\/Microbiology?alt=json-in-script\u0026max-results=5"},{"rel":"alternate","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/search\/label\/Microbiology"},{"rel":"hub","href":"http://pubsubhubbub.appspot.com/"},{"rel":"next","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/-\/Microbiology\/-\/Microbiology?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":{"$t":"360"},"openSearch$startIndex":{"$t":"1"},"openSearch$itemsPerPage":{"$t":"5"},"entry":[{"id":{"$t":"tag:blogger.com,1999:blog-2032508520370173515.post-2988561077344217931"},"published":{"$t":"2023-11-24T21:28:00.000+05:30"},"updated":{"$t":"2023-11-24T21:28:08.647+05:30"},"category":[{"scheme":"http://www.blogger.com/atom/ns#","term":"Microbiology"},{"scheme":"http://www.blogger.com/atom/ns#","term":"Validation"}],"title":{"type":"text","$t":"What is Disinfectant Validation?"},"content":{"type":"html","$t":"Disinfectant validation is the process of determining whether a disinfectant is effective in cleaning a surface. The purpose of this process is to ensure that the disinfectant is effective and does not cause any harm to the environment or the people using it.\u003Cspan\u003E\u003C\/span\u003E\u003Ca href=\"https:\/\/www.pharmaguideline.com\/2022\/07\/what-is-disinfectant-validation.html#more\"\u003EContinue reading »\u003C\/a\u003E"},"link":[{"rel":"replies","type":"application/atom+xml","href":"https:\/\/www.pharmaguideline.com\/feeds\/2988561077344217931\/comments\/default","title":"Post Comments"},{"rel":"replies","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/2022\/07\/what-is-disinfectant-validation.html#comment-form","title":"0 Comments"},{"rel":"edit","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/2988561077344217931"},{"rel":"self","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/2988561077344217931"},{"rel":"alternate","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/2022\/07\/what-is-disinfectant-validation.html","title":"What is Disinfectant Validation?"}],"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\/AVvXsEhQlZ__-Lfw3CpDeapQNbC2nlcG0mJiJbZaspqUHkiHMd7P5zWWWW4wyqmxKyWGeL32lql7UUk6ec1n9hAl5kpEpAZTgpowJ4a-BkJuflSVvTCFZuIEFdWolA3RpiGpnQmCwizBBG7IaWY3eElIeYOAhyUAgUSbnHNNA6bBCrIAs6xkqv07YzIkO7a-Lg\/s72-w320-h225-c\/disinfectants-validation.png","height":"72","width":"72"},"thr$total":{"$t":"0"}},{"id":{"$t":"tag:blogger.com,1999:blog-2032508520370173515.post-3982179477830961465"},"published":{"$t":"2023-08-22T23:30:00.000+05:30"},"updated":{"$t":"2023-08-22T23:30:06.689+05:30"},"category":[{"scheme":"http://www.blogger.com/atom/ns#","term":"GMP"},{"scheme":"http://www.blogger.com/atom/ns#","term":"Microbiology"},{"scheme":"http://www.blogger.com/atom/ns#","term":"Sterility"}],"title":{"type":"text","$t":"Difference Between Dynamic and Static Pass Box"},"content":{"type":"html","$t":"In pharmaceutical manufacturing industries, pass boxes are normally used to transfer a particular material between two areas generally of different cleanliness levels. The boxes can be said to transfer the materials from a high level of cleanliness to a lower level of cleanliness or vice-versa. The pass boxes while transferring the material, help to prevent air from flowing from one area to another. Pass boxes are made of stainless steel which is powder coated.\u003Cbr\u003E\n\u003Ca href=\"https:\/\/www.pharmaguideline.com\/2017\/10\/difference-between-dynamic-and-static-passbox.html#more\"\u003EContinue reading »\u003C\/a\u003E"},"link":[{"rel":"replies","type":"application/atom+xml","href":"https:\/\/www.pharmaguideline.com\/feeds\/3982179477830961465\/comments\/default","title":"Post Comments"},{"rel":"replies","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/2017\/10\/difference-between-dynamic-and-static-passbox.html#comment-form","title":"12 Comments"},{"rel":"edit","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/3982179477830961465"},{"rel":"self","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/3982179477830961465"},{"rel":"alternate","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/2017\/10\/difference-between-dynamic-and-static-passbox.html","title":"Difference Between Dynamic and Static Pass Box"}],"author":[{"name":{"$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$media":"http://search.yahoo.com/mrss/","url":"https:\/\/2.bp.blogspot.com\/-3c8q5P_AF-0\/WfXvxskd6CI\/AAAAAAAAG7s\/WSS4DCRLd7wm4PgVPQgLUzkXIpHU4z12wCLcBGAs\/s72-c\/pass-box.jpg","height":"72","width":"72"},"thr$total":{"$t":"12"}},{"id":{"$t":"tag:blogger.com,1999:blog-2032508520370173515.post-4167202282650972442"},"published":{"$t":"2023-08-01T22:39:00.000+05:30"},"updated":{"$t":"2023-08-01T22:39:21.780+05:30"},"category":[{"scheme":"http://www.blogger.com/atom/ns#","term":"Engineering"},{"scheme":"http://www.blogger.com/atom/ns#","term":"Microbiology"},{"scheme":"http://www.blogger.com/atom/ns#","term":"Sterile"}],"title":{"type":"text","$t":"Smoke Study in Cleanroom Areas"},"content":{"type":"html","$t":"The smoke study also known as dynamic air visualization study is the key qualification, maintenance and monitoring of facility to ensure the final product is free from \u003Ca href=\"https:\/\/www.pharmaguideline.com\/2018\/06\/prevention-of-microbial-contamination-in-manufacturing.html\" target=\"_blank\"\u003Econtamination\u003C\/a\u003E in a processing company. The smoke study in cleanroom area is conducted to visually confirm unidirectional airflow exiting \u003Ca href=\"https:\/\/www.pharmaguideline.com\/2012\/03\/high-efficiency-particulate-air-hepa.html\" target=\"_blank\"\u003EHigh Efficiency Particulate Air\u003C\/a\u003E (HEPA) or Ultra Low Particulate Air (ULPA) filters in a manufacturing clean room.\u003Cbr\u003E\n\u003Ca href=\"https:\/\/www.pharmaguideline.com\/2018\/09\/smoke-study-in-cleanroom-area.html#more\"\u003EContinue reading »\u003C\/a\u003E"},"link":[{"rel":"replies","type":"application/atom+xml","href":"https:\/\/www.pharmaguideline.com\/feeds\/4167202282650972442\/comments\/default","title":"Post Comments"},{"rel":"replies","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/2018\/09\/smoke-study-in-cleanroom-area.html#comment-form","title":"1 Comments"},{"rel":"edit","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/4167202282650972442"},{"rel":"self","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/4167202282650972442"},{"rel":"alternate","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/2018\/09\/smoke-study-in-cleanroom-area.html","title":"Smoke Study in Cleanroom Areas"}],"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:\/\/2.bp.blogspot.com\/-TKXUhKJhj8Y\/W5lQqqrom8I\/AAAAAAAAHmc\/V4XjNw4ss1gMYwOoMrdYM-b3TCZKVEnMwCLcBGAs\/s72-c\/smoke-test.jpg","height":"72","width":"72"},"thr$total":{"$t":"1"}},{"id":{"$t":"tag:blogger.com,1999:blog-2032508520370173515.post-1591390556947764870"},"published":{"$t":"2023-03-26T21:57:00.008+05:30"},"updated":{"$t":"2023-06-16T10:57:37.333+05:30"},"category":[{"scheme":"http://www.blogger.com/atom/ns#","term":"HVAC"},{"scheme":"http://www.blogger.com/atom/ns#","term":"Microbiology"},{"scheme":"http://www.blogger.com/atom/ns#","term":"Sterile"}],"title":{"type":"text","$t":"Maintenance of Aseptic Conditions in Pharmaceutical Sterile Areas"},"content":{"type":"html","$t":"Aseptic area is used to manufacture sterile products in pharmaceuticals. The aseptic area is maintained by following strict cleaning and disinfection procedures. Maintenance of aseptic conditions in the sterile area can be challenging. Various aspects of aseptic area maintenance are discussed in this article.\u003Cspan\u003E\u003C\/span\u003E\u003Ca href=\"https:\/\/www.pharmaguideline.com\/2023\/03\/maintenance-of-aseptic-conditions.html#more\"\u003EContinue reading »\u003C\/a\u003E"},"link":[{"rel":"replies","type":"application/atom+xml","href":"https:\/\/www.pharmaguideline.com\/feeds\/1591390556947764870\/comments\/default","title":"Post Comments"},{"rel":"replies","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/2023\/03\/maintenance-of-aseptic-conditions.html#comment-form","title":"0 Comments"},{"rel":"edit","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/1591390556947764870"},{"rel":"self","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/1591390556947764870"},{"rel":"alternate","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/2023\/03\/maintenance-of-aseptic-conditions.html","title":"Maintenance of Aseptic Conditions in Pharmaceutical Sterile Areas"}],"author":[{"name":{"$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$media":"http://search.yahoo.com/mrss/","url":"https:\/\/1.bp.blogspot.com\/-qqriZV17TOw\/W4MA4sCin2I\/AAAAAAAAHiI\/iB8PCrHrYpEIvYfCPRqo0v_r5zpO-6-MACLcBGAs\/s72-c\/aseptic-area.jpg","height":"72","width":"72"},"thr$total":{"$t":"0"}},{"id":{"$t":"tag:blogger.com,1999:blog-2032508520370173515.post-6401999300455888472"},"published":{"$t":"2022-10-01T12:00:00.002+05:30"},"updated":{"$t":"2023-06-16T10:49:34.626+05:30"},"category":[{"scheme":"http://www.blogger.com/atom/ns#","term":"GMP"},{"scheme":"http://www.blogger.com/atom/ns#","term":"Microbiology"},{"scheme":"http://www.blogger.com/atom/ns#","term":"Non-sterile"}],"title":{"type":"text","$t":"How to Improve Microbiological Control of Non-Sterile Pharmaceuticals"},"content":{"type":"html","$t":"\u003Cdiv style=\"text-align: justify;\"\u003EMicroorganisms are present everywhere in the environment and can contaminate pharmaceutical products during production. To ensure patient safety, it is important to have effective microbiological control measures in place during the manufacture of non-sterile pharmaceuticals. In this article, we will discuss some key tips on how to improve microbiological control within your facility.\u003C\/div\u003E\u003Cspan\u003E\u003C\/span\u003E\u003Ca href=\"https:\/\/www.pharmaguideline.com\/2022\/10\/improve-microbiological-control-non-sterile.html#more\"\u003EContinue reading »\u003C\/a\u003E"},"link":[{"rel":"replies","type":"application/atom+xml","href":"https:\/\/www.pharmaguideline.com\/feeds\/6401999300455888472\/comments\/default","title":"Post Comments"},{"rel":"replies","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/2022\/10\/improve-microbiological-control-non-sterile.html#comment-form","title":"0 Comments"},{"rel":"edit","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/6401999300455888472"},{"rel":"self","type":"application/atom+xml","href":"https:\/\/www.blogger.com\/feeds\/2032508520370173515\/posts\/default\/6401999300455888472"},{"rel":"alternate","type":"text/html","href":"https:\/\/www.pharmaguideline.com\/2022\/10\/improve-microbiological-control-non-sterile.html","title":"How to Improve Microbiological Control of Non-Sterile 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\/AVvXsEiJ6DWhCSxMYeOVAslFgNyIb4YSCeJZhZ00Q3HE7OoLQXjok_9xW-acU8ilduVy0KfO_5hZ0qHzkeI46tCECtwYTv9XQg65OW4fMHslFWkhGitmnoj7xc4gB9UIK4ZA5rU5bSD4PGGT2GwnkC-7ZQ5uZFL6Ko0eqTB3jWbxKZ_-2AU1dgPDgORGT8chqA\/s72-w320-h272-c\/microbial%20quality.png","height":"72","width":"72"},"thr$total":{"$t":"0"}}]}});