Novotech announced today the acquisition of EastHORN, a European CRO with clinical, medical and regulatory expertise in multiple strategically important locations across the continent. The acquisition is part of Novotech’s global expansion program. EastHORN was established in 2004 and has over 250 employees.
The acquisition means biotech clients can access Novotech’s unique and unparalleled suite of early to late-phase CRO services across Europe and the US, with a specialist focus on Asia Pacific where the company has built a reputation for delivering high-quality expedited clinical trials.
Novotech CEO Dr. John Moller said:
“This acquisition is a strategic move to further expand our CRO operations and provide biotech clients with in-country expertise across Asia-Pacific, North America, and Europe to deliver their global drug development programs.
EastHORN and Novotech have been working together for many years and we share a culture of clinical excellence in biotech drug development. EastHORN which is retaining its brand, is now a Novotech company and will be integrated into our systems and processes so clients benefit from working with one CRO globally.
Clients can now access our exceptional European infrastructure, local knowledge, site relationships and access to diverse patient populations.”
EastHORN Executive Chairman Iain Gordon said:
“I first started working on clinical projects with Novotech 15 years ago and have always been impressed by the quality of their services and their client-focused approach. EastHORN has been working closely with Novotech for over a decade now and have many friends within the Novotech team. This is a natural next step for our group and my colleagues and I are excited to become part of Novotech’s global operations to support biotech clients’ clinical programs.
In particular, we can now offer our clients access to Novotech’s team of experts across Asia-Pacific and the US including project management, regulatory, clinical, medical and biometrics, while our team’s European expertise can advance clinical development in Europe for Novotech clients.
We work with similar-sized biotechs and small to mid-size pharma companies and have experience across the same therapeutic areas, so this is an excellent cultural and strategic fit.”
Novotech has decades of biotech drug development experience, exceptional site and investigator relationships, access to vast patient populations, and a project management approach focused on problem-solving, ownership and flexibility. Consistent investment in advanced training and technology combines to deliver an exceptional full-service biotech CRO solution.
Novotech has recently been recognised with significant CRO awards including the Asia-Pacific Biotech CRO of the Year by Frost & Sullivan, benchmarked as a top 10 CRO among the world’s leading CROs, a finalist in the prestigious Scrip awards, and has just been awarded the Gene & Cell Therapy Excellence Award.
In Asia Pacific Novotech has more than 50 Leading Site Partnership agreements with major medical research institutions which delivers exclusive benefits for sponsors.
媒體聯絡人
Toyna Chin
關於Novotech Novotech-CRO.com
Novotech作為一家可提供全方位服務的國際性受託研究機構 (CRO) 和科學諮詢公司,深受生物科技公司以及中小型製藥公司的信賴,引領其在各個階段的藥物開發。
公司在全球各地擁有30多個辦公據點,主要分佈在亞太地區、北美和歐洲,並與5000多個試驗機構建立了緊密的合作關係,為客戶提供豐富的臨床試驗資源網絡,幫助客戶輕鬆進軍關鍵試驗區域,廣泛接觸不同的受試者群體,推動變革性療法更快嘉惠患者。
透過以客戶為中心的服務模式,Novotech無縫整合人才、流程和技術,提供定制化解決方案,加速變革療法快速上市。透過建立緊密的合作夥伴關係,Novotech堅定不移地支援客戶實現研究目標,賦能創新,推動全球醫療健康發展。憑藉在臨床試驗執行和創新方面的卓越表現,Novotech已榮獲多項殊榮,包括連續19年蟬聯Frost & Sullivan CRO年度公司獎 (Frost & Sullivan CRO Company of the Year)。憑藉深厚的臨床領域與監管專業知識,再結合對當地市場的深刻洞察,公司致力於簡化臨床試驗流程,提升資料分析,並加快受試者招募策略的實施。
Novotech與客戶攜手並進,加速科學研發成果轉化為療法,改善全球患者結果,充分體現我們推動創新、實現卓越成果的使命。
如需瞭解更多資訊或與專家團隊成員洽談,請造訪www.Novotech-CRO.com