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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노보텍(Novotech) 소개

1997년 설립된 노보텍은 글로벌 full-service CRO이며 바이오텍과 제약회사와의 파트너십을 통해 임상의 모든 단계에서 혁신적이면서도 새로운 치료제 개발을 가속하는 데 주력하고 있습니다.  

노보텍은 CRO 업계에서의 선도적인 역할을 인정받아 다수의 권위 있는 상을 수상하였습니다. 2024년에는 Frost & Sullivan의 Global Biotech CRO Award, Clinical Trials Arena Award for Excellence in Business Expansion, Marketing, and Innovation, Employer of Choice, 미국 Great Place to Work 인증, Brandon Hall Gold Award를 수상하였으며, 2023년에는 CRO Leadership Award와 Asia Pacific Cell & Gene Therapy Clinical Trials Excellence를 수상하였습니다. 또한, 2006년부터 Asia-Pacific Contract Research Organization Company of the Year Award를 수상하며 업계에서의 입지를 공고히 하고 있습니다.

노보텍은 연구소, 임상 1상 시험 기관, 약물 개발 컨설팅 서비스, 규제 전문성 등 종합적인 서비스를 제공하며, 1상에서 4상까지의 임상시험과 생물학적 동등성 연구를 포함해 5000건 이상의 임상 프로젝트에 참여한 경험이 있습니다. 노보텍은 전 세계 지역에 걸쳐 34개 지사와 3000명 이상의 직원을 두고 있으며 신뢰할 수 있는 완전한 형태의 전략 파트너입니다.  

더 자세한 정보나 임상시험 관련 상담을 원하신다면, 노보텍 공식 웹사이트를 (www.Novotech-CRO.com) 방문하시기 바랍니다.  

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