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.

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Novotech是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,在藥物研發的各個階段提供指導,深受生物技術公司及中小型製藥公司的信賴。

Novotech的業務涉及全球多個國家和地區,在亞太地區、北美和歐洲設有30多個辦公據點,並與7,000多個試驗機構建立了緊密的合作關係,透過提供關鍵臨床試驗資源網絡、廣泛接觸不同的受試者群體,幫助客戶將前沿的治療方法加速推向市場。

Novotech透過以客戶為中心的服務模式,將人員、流程和技術無縫整合,提供定制化解決方案,推動變革性的治療方法進入市場。Novotech採用真正的合作夥伴關係模式,堅定地致力於幫助客戶取得成功、推動創新並促進全球醫療保健的發展。

Novotech憑藉卓越的臨床試驗執行和創新能力獲得了眾多業界榮譽。Novotech在臨床以及法規方面深厚的專業知識,以及對本地市場的深刻洞察,使其能夠為臨床試驗的順利進行、資料分析的強化以及加速受試者招募策略方面提供有力支援。

Novotech與客戶攜手,將科學進步轉化為能夠改善全球健康狀況的治療方法,實踐推動創新、創造卓越成果的使命。

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