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style="border-radius:0px 0px 0px 0px;width:100%;column-count:1"><p>News</p></div></div><div id="outer" data-widget="horizontal-rule-widget" style="background-color:transparent;padding:0px 24px 0px 24px" class="Widget-module_outer__PBh8P HorizontalRule-module_outer__3UqSE"><div id="inner" style="border-radius:0px 0px 0px 0px;width:100%"><hr style="border-top-style:solid;border-top-width:3px;border-top-color:#a31f29"/></div></div><div id="outer" data-widget="heading-widget" style="background-color:transparent;padding:0px 24px 16px 24px;text-align:left;font-size:100%;line-height:1.3;letter-spacing:0" class="Widget-module_outer__PBh8P Heading-module_container__uHf-4"><div id="inner" style="border-radius:0px 0px 0px 0px;width:100%"><h2><span style="font-family:"Roboto Slab"" class="__bold">Strategic alliance announced between Recipharm and Exela for sterile manufacturing capabilities in the US</span></h2></div></div><div id="outer" data-widget="paragraph-widget" style="background-color:transparent;padding:0px 24px 8px 24px;text-align:left;font-size:100%;line-height:1.3;letter-spacing:0" class="Widget-module_outer__PBh8P Paragraph-module_container__-DJUN"><div id="inner" style="border-radius:0px 0px 0px 0px;width:100%;column-count:1"><p><span class="__bold" style="color:rgb(28,28,28)">Recipharm and Exela have announced that they have entered into an exclusive strategic alliance. The alliance between the two contract development and manufacturing organisations (CDMOs) aims to enhance sterile manufacturing capabilities in the US. </span><span class="__bold" style="color:rgb(28, 28, 28)">As part of the alliance, Recipharm will be able to take advantage of Exela’s state-of-the-art manufacturing plant in Lenoir, NC, US. </span><span class="__bold" style="color:rgb(28, 28, 28)">The plant manufactures sterile injectable pharmaceuticals in vials and pre-filled syringes (PFS), and proved its efficiency and efficacy during the COVID-19 pandemic.</span></p></div></div><div id="outer" data-widget="image-widget" style="background-color:transparent;padding:8px 24px 16px 24px;min-height:auto" class="Widget-module_outer__PBh8P"><div id="inner" class="Image-module_container__8raIv Image-module_container-noflex__-J1PG" style="border-radius:0px 0px 0px 0px;width:100%;min-height:auto"><picture class="Image-module_picture__gw1zY Image-module_loading__FfyPr"><source type="image/jpeg" srcSet="https://cdn.magloft.com/pdf-import/1125/images/img_5-1.jpg?optimizer=image&width=192 192w,https://cdn.magloft.com/pdf-import/1125/images/img_5-1.jpg?optimizer=image&width=384 384w,https://cdn.magloft.com/pdf-import/1125/images/img_5-1.jpg?optimizer=image&width=768 768w,https://cdn.magloft.com/pdf-import/1125/images/img_5-1.jpg?optimizer=image&width=1536 1536w" sizes="(min-width: 768px) 768px, 100vw"/><img src="https://cdn.magloft.com/pdf-import/1125/images/img_5-1.jpg?optimizer=image&width=768" srcSet="https://cdn.magloft.com/pdf-import/1125/images/img_5-1.jpg?optimizer=image&width=192 192w,https://cdn.magloft.com/pdf-import/1125/images/img_5-1.jpg?optimizer=image&width=384 384w,https://cdn.magloft.com/pdf-import/1125/images/img_5-1.jpg?optimizer=image&width=768 768w,https://cdn.magloft.com/pdf-import/1125/images/img_5-1.jpg?optimizer=image&width=1536 1536w" sizes="(min-width: 768px) 768px, 100vw" class="Image-module_image__w4slc" width="100%" height="431" decoding="async" alt="Image" style="height:auto;width:100%"/></picture></div></div><div id="outer" data-widget="paragraph-widget" style="background-color:transparent;padding:0px 24px 8px 24px;text-align:left;font-size:100%;line-height:1.3;letter-spacing:0" class="Widget-module_outer__PBh8P Paragraph-module_container__-DJUN"><div id="inner" style="border-radius:0px 0px 0px 0px;width:100%;column-count:1"><p>Access to the US Food and Drug Administration (FDA)-accredited plant allows Recipharm to improve its sterile manufacturing footprint in the US, with now over 100 million units capable of being produced to the FDA’s Center for Drug Evaluation and Research (CDER) and the Center for Biologics Evaluation and Research (CBER) specifications. Part of this manufacturing scope is due to Exela’s advanced manufacturing processes, which include automatic visual inspection, automated packaging and auto-injector assembly. This helps position the plant as a prime option for producing glucagon-like peptide (GLP)-1 drugs, sterile products such as vaccines and biologics, and highly targeted biopharma drugs such as antibody drug conjugates (ADCs).</p></div></div><div id="outer" data-widget="paragraph-widget" style="background-color:transparent;padding:0px 24px 8px 24px;text-align:left;font-size:100%;line-height:1.3;letter-spacing:0" class="Widget-module_outer__PBh8P Paragraph-module_container__-DJUN"><div id="inner" style="border-radius:0px 0px 0px 0px;width:100%;column-count:1"><p>As part of the agreement, the site will now adopt international compliance practices – in addition to the current FDA-compliant standards – to better align with Recipharm’s operational quality and standards, allowing additional international markets and customers to be targeted. Recipharm will also offer its analytical capabilities, commercial expertise and manufacturing support to Exela. ReciBioPharm, its biologics division, will also collaborate with Exela on its advanced therapeutic medicinal products (ATMP) capabilities.</p></div></div><div id="outer" data-widget="paragraph-widget" style="background-color:transparent;padding:0px 24px 8px 24px;text-align:left;font-size:100%;line-height:1.3;letter-spacing:0" class="Widget-module_outer__PBh8P Paragraph-module_container__-DJUN"><div id="inner" style="border-radius:0px 0px 0px 0px;width:100%;column-count:1"><p>Greg Behar, CEO of Recipharm, commented: “We are excited about this strategic alliance with Exela, which significantly enhances our manufacturing footprint in the US. This partnership aligns with our commitment to prov ide high quality manufacturing solutions and expand our capabilities in the production of sterile products, such as GLP-1, peptides, biologics, ADCs and other critical pharmaceuticals.”</p></div></div><div id="outer" data-widget="paragraph-widget" style="background-color:transparent;padding:0px 24px 8px 24px;text-align:left;font-size:100%;line-height:1.3;letter-spacing:0" class="Widget-module_outer__PBh8P Paragraph-module_container__-DJUN"><div id="inner" style="border-radius:0px 0px 0px 0px;width:100%;column-count:1"><p>“Recipharm is a highly respected CDMO with worldw ide reach. We are honoured and excited to be Recipharm’s exclusive US partner. This collaboration offers a unique and efficient CDMO platform for biopharma customers that seek to participate in both US and EU markets and are looking for scale, speed and versatility with experience in delivering complex projects,” added Phanesh Koneru PhD LLM, president and CEO of Exela.</p></div></div><div id="outer" data-widget="paragraph-widget" style="background-color:transparent;padding:0px 24px 8px 24px;text-align:left;font-size:100%;line-height:1.3;letter-spacing:0" class="Widget-module_outer__PBh8P Paragraph-module_container__-DJUN"><div id="inner" style="border-radius:0px 0px 0px 0px;width:100%;column-count:1"><p>Recipharm is a CDMO with facilities in Sweden, France, Germany, Italy, Spain, Portugal, India and the UK. Its headquarters are in Sweden. 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The alliance between the two contract development and manufacturing organisations (CDMOs) aims to enhance sterile manufacturing capabilities in the US. As part of the alliance, Recipharm will be able to take advantage of Exela’s state-of-the-art manufacturing plant in Lenoir, NC, US.","image":"https://cdn.magloft.com/pdf-import/1125/images/img_5-1.jpg","cover":"https://cdn.magloft.com/publication-14882/screenshots/articles/266506.jpg?ts=1728470381","date":1728601200000,"unlockType":"free","categories":[],"pdfPageId":"JbkUYUDsyYzX","visible":true,"showOnToc":true,"bookmark":false,"position":10,"publicationId":14882,"pwaOptinId":null,"seoDescription":"Recipharm and Exela have announced that they have entered into an exclusive strategic alliance. The alliance between the two contract development and manufacturing organisations (CDMOs) aims to enhance sterile manufacturing capabilities in the US.","classificationIds":[],"pwaSubscriptionIds":[],"source":"typeloft2","trending":false,"html":"\u003cpage-widget padding=\"16 0 24 0\"\u003e\u003cparagraph-widget padding=\"0 24 0 24\"\u003eNews\u003c/paragraph-widget\u003e\u003chorizontal-rule-widget padding=\"0 24 0 24\" color=\"#a31f29\"\u003e\u003c/horizontal-rule-widget\u003e\u003cheading-widget padding=\"0 24 16 24\" type=\"h2\"\u003e\u003cspan style=\"font-family: \u0026quot;Roboto Slab\u0026quot;;\" class=\"__bold\"\u003eStrategic alliance announced between Recipharm and Exela for sterile manufacturing capabilities in the US\u003c/span\u003e\u003c/heading-widget\u003e\u003cparagraph-widget padding=\"0 24 8 24\"\u003e\u003cspan class=\"__bold\" style=\"color: rgb(28,28,28)\"\u003eRecipharm and Exela have announced that they have entered into an exclusive strategic alliance. The alliance between the two contract development and manufacturing organisations (CDMOs) aims to enhance sterile manufacturing capabilities in the US. \u003c/span\u003e\u003cspan class=\"__bold\" style=\"color: rgb(28, 28, 28)\"\u003eAs part of the alliance, Recipharm will be able to take advantage of Exela’s state-of-the-art manufacturing plant in Lenoir, NC, US. \u003c/span\u003e\u003cspan class=\"__bold\" style=\"color: rgb(28, 28, 28)\"\u003eThe plant manufactures sterile injectable pharmaceuticals in vials and pre-filled syringes (PFS), and proved its efficiency and efficacy during the COVID-19 pandemic.\u003c/span\u003e\u003c/paragraph-widget\u003e\u003cimage-widget padding=\"8 24 16 24\" aspect-ratio=\"0.5606936416184971\" magnify-label=\"center\" source=\"https://cdn.magloft.com/pdf-import/1125/images/img_5-1.jpg#image/jpeg\"\u003e\u003c/image-widget\u003e\u003cparagraph-widget padding=\"0 24 8 24\"\u003eAccess to the US Food and Drug Administration (FDA)-accredited plant allows Recipharm to improve its sterile manufacturing footprint in the US, with now over 100 million units capable of being produced to the FDA’s Center for Drug Evaluation and Research (CDER) and the Center for Biologics Evaluation and Research (CBER) specifications. Part of this manufacturing scope is due to Exela’s advanced manufacturing processes, which include automatic visual inspection, automated packaging and auto-injector assembly. This helps position the plant as a prime option for producing glucagon-like peptide (GLP)-1 drugs, sterile products such as vaccines and biologics, and highly targeted biopharma drugs such as antibody drug conjugates (ADCs).\u003c/paragraph-widget\u003e\u003cparagraph-widget padding=\"0 24 8 24\"\u003eAs part of the agreement, the site will now adopt international compliance practices – in addition to the current FDA-compliant standards – to better align with Recipharm’s operational quality and standards, allowing additional international markets and customers to be targeted. Recipharm will also offer its analytical capabilities, commercial expertise and manufacturing support to Exela. ReciBioPharm, its biologics division, will also collaborate with Exela on its advanced therapeutic medicinal products (ATMP) capabilities.\u003c/paragraph-widget\u003e\u003cparagraph-widget padding=\"0 24 8 24\"\u003eGreg Behar, CEO of Recipharm, commented: “We are excited about this strategic alliance with Exela, which significantly enhances our manufacturing footprint in the US. This partnership aligns with our commitment to prov ide high quality manufacturing solutions and expand our capabilities in the production of sterile products, such as GLP-1, peptides, biologics, ADCs and other critical pharmaceuticals.”\u003c/paragraph-widget\u003e\u003cparagraph-widget padding=\"0 24 8 24\"\u003e“Recipharm is a highly respected CDMO with worldw ide reach. We are honoured and excited to be Recipharm’s exclusive US partner. This collaboration offers a unique and efficient CDMO platform for biopharma customers that seek to participate in both US and EU markets and are looking for scale, speed and versatility with experience in delivering complex projects,” added Phanesh Koneru PhD LLM, president and CEO of Exela.\u003c/paragraph-widget\u003e\u003cparagraph-widget padding=\"0 24 8 24\"\u003eRecipharm is a CDMO with facilities in Sweden, France, Germany, Italy, Spain, Portugal, India and the UK. Its headquarters are in Sweden. Exela is a software comapany that specialises in business process automation, based in the US.\u003c/paragraph-widget\u003e\u003c/page-widget\u003e","keywordPhrase":"alliance","articleAssets":[{"url":"https://cdn.magloft.com/reader/fonts/roboto-slab.css","extension":"css","contentType":"text/css"},{"url":"https://cdn.magloft.com/reader/fonts/open-sans.css","extension":"css","contentType":"text/css"},{"url":"https://cdn.magloft.com/pdf-import/1125/images/img_5-1.jpg","extension":"jpeg","contentType":"image/jpeg"}]},"publicationId":14882},"__N_SSG":true},"page":"/domains/[domain]/articles/[slug]","query":{"domain":"www.pharmafocus.com","slug":"strategic-alliance-announced-between-recipharm-and-exela-for-ste"},"buildId":"U1LT7ce93wR6IyWFJCllT","isFallback":false,"gsp":true,"scriptLoader":[]}</script></body></html>