{"id":314,"date":"2024-02-16T12:59:27","date_gmt":"2024-02-16T03:59:27","guid":{"rendered":"https:\/\/cm-plus.co.jp\/id\/?p=314"},"modified":"2025-05-02T14:49:46","modified_gmt":"2025-05-02T05:49:46","slug":"2024_0216","status":"publish","type":"post","link":"https:\/\/cm-plus.co.jp\/id\/news\/event\/2024_0216\/","title":{"rendered":"We Will Exhibit and Present a Seminar at CPHI Japan 2024 (International Pharmaceutical Development Exhibition) _completed"},"content":{"rendered":"<div class=\"imgBox\">\n<p>CM Plus will be exhibiting at \u201cCPHI Japan\u201d (International Pharmaceutical Development Exhibition), held from April 17th (Wed) to 19th (Fri), 2024, at Tokyo Big Sight. Please visit our booth.<\/p>\n<p class=\"ttl\">CM Plus Booth Number:<span class=\"number\">4W-02<\/span><\/p>\n<div class=\"photo\"><a href=\"https:\/\/www.cphijapan.com\/\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-315\" src=\"https:\/\/cm-plus.co.jp\/id\/wp-content\/uploads\/2024\/04\/thumb.webp\" alt=\"\" width=\"480\" height=\"320\" srcset=\"https:\/\/cm-plus.co.jp\/id\/wp-content\/uploads\/2024\/04\/thumb.webp 480w, https:\/\/cm-plus.co.jp\/id\/wp-content\/uploads\/2024\/04\/thumb-300x200.webp 300w\" sizes=\"auto, (max-width: 480px) 100vw, 480px\" \/><\/a><\/div>\n<p>In addition, our engineers and consultants will be presenting on trending topics at the following conference venue.<\/p>\n<p class=\"comLinkP02\"><a href=\"https:\/\/www.cphi.com\/japan\/en\/home.html\" target=\"_blank\" rel=\"noopener noreferrer\">the official CPHI website<\/a><\/p>\n<\/div>\n<h2 class=\"headLine05\">Seminar Date: April 17th (Wed)<\/h2>\n<h3 class=\"headLine06\">Conference [Venue 6A] (Inside East Hall 6)<\/h3>\n<div class=\"comSeminar\">\n<p class=\"title\"><span class=\"topSpan\"><span class=\"category\">6A-04<\/span><span class=\"time\">14:00-14:40<\/span><\/span><span class=\"ttl\">Key Points in Process Design During the Basic Planning of API Plants<\/span><\/p>\n<p>The main challenge in the basic planning of pharmaceutical API is the process of constructing the manufacturing scale process flow from pilot scale test results. For pharmaceutical APIs, most processes are batch processes from a quality assurance perspective, and the rates of heat transfer and diffusion affect the process productivity, which in turn significantly impacts the plant scale and project cost.<br \/>\nIn this presentation, we will outline how the documents created during the basic planning phase relate to each other from the perspective of process optimization. We will then discuss the impacts of rates of heat transfer and diffusion on plant scale using specific calculations.<\/p>\n<div class=\"staffBox\">\n<div class=\"photoBox\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-320\" src=\"https:\/\/cm-plus.co.jp\/id\/wp-content\/uploads\/2024\/04\/news_photo01.webp\" alt=\"\" width=\"220\" height=\"300\" \/><\/div>\n<div class=\"textBox\">\n<p><span class=\"top\">Speaker<\/span>Takashi Yahiro<br \/>\nHead of Engineering &#038; Design Division, Engineering Business Department<br \/>\nCM Plus Corporation<\/p>\n<\/div>\n<\/div>\n<\/div>\n<h3 class=\"headLine06\">Conference [Venue 4C] (Inside East Hall 4)<\/h3>\n<div class=\"comSeminar\">\n<p class=\"title\"><span class=\"topSpan\"><span class=\"category\">4C-03<\/span><span class=\"time\">13:00-13:45<\/span><\/span><span class=\"ttl\">Project Execution Incorporating the Concept of Lean Qualification Approach<\/span><\/p>\n<p>Lean Qualification Approach (LQA) is a method proposed by CM Plus for efficiently conducting qualifications during the installation phase of pharmaceutical and medical device manufacturing facilities while complying with regulatory requirements. In 2015, PIC\/S Annex 15 was revised to specify requirements for validation. Additionally, ISPE\u2019s Baseline Guide Volume 5 Commissioning and Qualification introduced the idea of utilizing FAT and SA for qualification. Based on these concepts, CM Plus has developed LQA as a qualification method incorporating risk assessment and has been refining it through practical application.<\/p>\n<p>This presentation will explain the benefits of adopting LQA and provide an overview of the methodology.<\/p>\n<div class=\"staffBox\">\n<div class=\"photoBox\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-322\" src=\"https:\/\/cm-plus.co.jp\/id\/wp-content\/uploads\/2024\/04\/news_photo02.webp\" alt=\"\" width=\"220\" height=\"300\" \/><\/div>\n<div class=\"textBox\">\n<p><span class=\"top\">Speaker<\/span>Takashi Ito<br \/>\nHead of Professional Services Division<br \/>\nCM Plus Corporation<\/p>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"comSeminar\">\n<p class=\"title\"><span class=\"topSpan\"><span class=\"category\">4C-05<\/span><span class=\"time\">15:45-16:30<\/span><\/span><span class=\"ttl\">Addressing Contamination Control Strategy (CCS) Following the Revision of PIC\/S GMP Annex 1<\/span><\/p>\n<p>This session will organize the basic concepts and requirements pertaining to the key term \u201cContamination Control Strategy (CCS)\u201d introduced in the revised PIC\/S GMP Annex 1 in 2022. We will explain how to formulate and document a CCS, referencing guidelines like the ECA, and introduce examples of CCS documentation.<\/p>\n<div class=\"staffBox\">\n<div class=\"photoBox\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-323\" src=\"https:\/\/cm-plus.co.jp\/id\/wp-content\/uploads\/2024\/04\/news_photo03.webp\" alt=\"\" width=\"220\" height=\"300\" \/><\/div>\n<div class=\"textBox\">\n<p><span class=\"top\">Speaker<\/span>Noriki Sakata<br \/>\nHead of Validation Department, Professional Services Division<br \/>\nCM Plus Corporation<\/p>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"comApplyBox\">\n<p class=\"ttl\">Please register for the above seminars here.<\/p>\n<div class=\"btn\"><a href=\"https:\/\/www.informa-japan.com\/cphifcj\/seminar\/index.php?category=101\" target=\"_blank\" rel=\"noopener\"><span class=\"wptag\">Seminar Program &#038; Registration (Visit the official CPHI website)<\/span><\/a><\/div>\n<\/div>\n<h2 class=\"headLine05\">Exhibition Overview<\/h2>\n<table style=\"border-collapse: collapse; width: 100%; height: 144px;\">\n<tbody>\n<tr style=\"height: 72px;\">\n<th style=\"width: 50%; height: 72px;\">Name<\/th>\n<td style=\"width: 50%; height: 72px;\">CPHI Japan 2023 (International Pharmaceutical Development Exhibition)<\/td>\n<\/tr>\n<tr style=\"height: 24px;\">\n<th style=\"width: 50%; height: 24px;\">Concurrent Events<\/th>\n<td style=\"width: 50%; height: 24px;\">Pharma IT &#038; Digital Health Expo 2024<br \/>\n\tMedtec Japan 2024 (Medical Device Design &#038; Manufacturing Exhibition)\n<\/td>\n<\/tr>\n<tr style=\"height: 24px;\">\n<th style=\"width: 50%; height: 24px;\">Date<\/th>\n<td style=\"width: 50%; height: 24px;\">April 17 (Wed), 18 (Thu), 19 (Fri), 2024<\/td>\n<\/tr>\n<tr style=\"height: 24px;\">\n<th style=\"width: 50%; height: 24px;\">Time<\/th>\n<td style=\"width: 50%; height: 24px;\">10:00 &#8211; 17:00 (Exhibition Hours)<\/td>\n<\/tr>\n<tr style=\"height: 24px;\">\n<th style=\"width: 50%; height: 24px;\">Venue<\/th>\n<td style=\"width: 50%; height: 24px;\">Tokyo Big Sight East Halls 4, 5, and 6<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p class=\"comLinkP02\"><a href=\"https:\/\/www.cphijapan.com\/\" target=\"_blank\" rel=\"noopener\">the official CPHI website<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>CM Plus will be exhibiting at \u201cCPHI Japan\u201d (International Pharmaceutical Development Exhibition), held from April 17th (Wed) to 19th (Fri), 2024, at Tokyo Big Sight. Please visit our booth. CM Plus Booth Number:4W-02 In addition, our engineers and consultants will be presenting on trending topics at the following conference venue. the official CPHI website Seminar Date: April 17th (Wed) Conference [Venue 6A] (Inside East Hall 6) 6A-0414:00-14:40Key Points in Process Design During the Basic Planning of API Plants The main challenge in the basic planning of pharmaceutical API is the process of constructing the manufacturing scale process flow from pilot scale test results. For pharmaceutical APIs, most processes are batch [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[3],"tags":[],"keywords":[],"class_list":["post-314","post","type-post","status-publish","format-standard","hentry","category-event"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v22.4 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>We Will Exhibit and Present a Seminar at CPHI Japan 2024 (International Pharmaceutical Development Exhibition) _completed\uff5cCM Plus<\/title>\n<meta name=\"description\" content=\"CM Plus will be exhibiting at \u201cCPHI Japan\u201d (International Pharmaceutical Development Exhibition), held from April 17th (Wed) to 19th (Fri), 2024, at Tokyo Big Sight. 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