{"id":8055,"date":"2021-09-27T16:02:01","date_gmt":"2021-09-27T21:02:01","guid":{"rendered":"https:\/\/bethematchbiotherapies.com\/?post_type=dt_portfolio&#038;p=8055"},"modified":"2024-04-16T12:00:32","modified_gmt":"2024-04-16T17:00:32","slug":"cell-therapy-industry-turning-point-whitepaper","status":"publish","type":"dt_portfolio","link":"https:\/\/bethematchbiotherapies.com\/resources\/cell-therapy-industry-turning-point-whitepaper\/","title":{"rendered":"A Cell Therapy Industry Turning Point"},"content":{"rendered":"<div class=\"wpb-content-wrapper\"><p>[vc_row][vc_column width=&#8221;2\/3&#8243;][vc_column_text]<strong>Starting material collection can set the fate of your final cell therapy product. Quality matters.<\/strong><\/p>\n<p>That\u2019s why your site qualification process\u2014including your quality system audit\u2014for each site is so important. But with the rapid proliferation of cell and gene therapies, current processes are unsustainable and could cripple cell collection site capacity.<\/p>\n<p>That could mean delays in your therapy development. There are solutions.<\/p>\n<p>In our Case In Point, the authors illustrate how standardization through a quality system audit program can create immediate efficiencies and reduce the risk of delays.<\/p>\n<p>Authors include:<\/p>\n<ul>\n<li>Heather Steinmetz, MPH, Quality Assistance Manager, UCLA Health Hematologic Malignancy\/Stem Cell Program<\/li>\n<li>Amy Hines, RN, BSN, Director, Collection Experience, National Marrow Donor Program\u00ae\/Be The Match\u00ae<\/li>\n<li>Richard Smith, Independent Consultant, Be The Match BioTherapies\u00ae<\/li>\n<\/ul>\n<p>[\/vc_column_text][\/vc_column][vc_column width=&#8221;1\/3&#8243;]<style type=\"text\/css\" data-type=\"the7_shortcodes-inline-css\">#default-btn-684f8e5926ef35c63172cda9cc82aedc {\n  border-radius: 100px;\n  font-size: 16px;\n  line-height: 18px;\n}\n.btn-shadow#default-btn-684f8e5926ef35c63172cda9cc82aedc {\n  box-shadow: 0 1px 6px rgba(0,0,0,0.12);\n  transition: box-shadow 0.2s ease-out, opacity 0.45s;\n}\n.btn-shadow#default-btn-684f8e5926ef35c63172cda9cc82aedc:hover {\n  box-shadow: 0 5px 11px 0 rgba(0,0,0,0.18), 0 4px 15px 0 rgba(0,0,0,0.15);\n}\n.btn-3d#default-btn-684f8e5926ef35c63172cda9cc82aedc {\n  box-shadow: 0px 2px 0px 0px #03121e;\n}\n.btn-3d#default-btn-684f8e5926ef35c63172cda9cc82aedc:hover {\n  box-shadow: 0px 2px 0px 0px #03121e;\n}\n.btn-flat#default-btn-684f8e5926ef35c63172cda9cc82aedc {\n  box-shadow: none;\n}\n.btn-flat#default-btn-684f8e5926ef35c63172cda9cc82aedc:hover {\n  box-shadow: none;\n}\n#default-btn-684f8e5926ef35c63172cda9cc82aedc.ico-right-side > i {\n  margin-right: 0px;\n  margin-left: 8px;\n}\n#default-btn-684f8e5926ef35c63172cda9cc82aedc > i {\n  margin-right: 8px;\n  font-size: 12px;\n}\n#default-btn-684f8e5926ef35c63172cda9cc82aedc:not(:hover) {\n  border-width: 0px;\n  color: #ffffff;\n  background: #00355e !important;\n  padding: 12px 18px 12px 18px;\n}\n#default-btn-684f8e5926ef35c63172cda9cc82aedc:not(:hover) * {\n  color: #ffffff;\n}\n#default-btn-684f8e5926ef35c63172cda9cc82aedc:hover {\n  border-width: 0px;\n  color: #b4bd00;\n  background: #00355e !important;\n  padding: 12px 18px 12px 18px;\n}\n#default-btn-684f8e5926ef35c63172cda9cc82aedc:hover * {\n  color: #b4bd00;\n}\n#default-btn-684f8e5926ef35c63172cda9cc82aedc.ico-right-side > i {\n  margin-right: 0px;\n  margin-left: 8px;\n}\n#default-btn-684f8e5926ef35c63172cda9cc82aedc > i {\n  margin-right: 8px;\n}\n<\/style><div class=\"btn-align-center\"><a href=\"\/wp-content\/uploads\/2024\/04\/NP21389_BioTherapies_Whitepaper_QSA_SM_2024-03-29_Digital.pdf\" class=\"default-btn-shortcode dt-btn link-hover-off btn-flat  vc_custom_1713286827508\" target=\"_blank\" id=\"default-btn-684f8e5926ef35c63172cda9cc82aedc\" style=\"width:240px;\" rel=\"noopener\"><span>DOWNLOAD REPORT<\/span><\/a><\/div>[\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"<p>[vc_row][vc_column width=&#8221;2\/3&#8243;][vc_column_text]Starting material collection can set the fate of your final cell therapy product. Quality matters. That\u2019s why your site qualification process\u2014including your quality system audit\u2014for each site is so important. But with the rapid proliferation of cell and gene therapies, current processes are unsustainable and could cripple cell collection site capacity. That could mean&hellip;<\/p>\n","protected":false},"author":15,"featured_media":8039,"comment_status":"closed","ping_status":"closed","template":"","dt_portfolio_category":[3282],"dt_portfolio_tags":[3305,3309,3308,3311,3310,3307,3327],"coauthors":[18],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v22.6 (Yoast SEO v22.6) - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>How QSA Standardization can Increase Collection Capacity<\/title>\n<meta name=\"description\" content=\"Learn how standardization through a quality system audit program can create immediate efficiencies and reduce the risk of cell therapy development delays.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/bethematchbiotherapies.com\/resources\/cell-therapy-industry-turning-point-whitepaper\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta 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