Novotech, the Asia Pacific centered biotech specialist CRO, presents “The Next Big Thing in Cancer Care” expert panel webinar in collaboration with eChinaHealth and the ASCO Breakthrough program committee.
Novotech’s Asia Pacific operations support expedited oncology clinical trials by offering access to vast patient populations, deep local regulatory knowledge, an extensive site and KOL network, and data quality excellence.
The Asia Pacific has seen a 100% growth in oncology trials during 2017 to 2021 and contributes to more than a third of the global clinical development of immune-oncology drugs.
“By the end of 2021 40% of active immuno-oncology clinical trials involved at least one location in the Asia-Pacific region, with majority of trials conducted in China, followed by Australia, South Korea, Japan and Taiwan,” according to GlobaData.
Register for the webinar here: Registration
- 5-6:30 pm (PST) / 8-9:30 pm (EST), Sunday, Jan. 8th, 2023 / 9-10:30 am, Monday, Jan 9th (Beijing Time)
- Zoom Webinar (No charge)
- English, with Chinese simultaneous translation
The webinar is moderated by Dr. Peter Yu, Physician-in-Chief, Hartford HealthCare, ASCO President for 2014-2015 term
The program features:
Drugging the Undrugable
- Dr. Lillian Siu, Professor, University of Toronto; Chair, Program Committee, ASCO Breakthrough 2023
CAR-T and Adoptive Cell Therapies
- Dr. David Lebwohl, CMO, Intellia Therapeutics
Precision Oncology, AI and Next Generation Multiomic Technology
- Dr. Melvin Chua Lee Kiang, Associate Professor, National Cancer Centre Singapore; Chair-Elect, Program Committee, ASCO Breakthrough 2023
Novotech has more than 50 Leading Site Partnership agreements with major medical research institutions in Asia Pacific delivering exclusive benefits for sponsors.
The latest industry research publication by GlobalData and Novotech found almost 50% of new trials have sites in Asia Pacific.
According to the new publication titled State of the Global Biotech Landscape: Where the Opportunities Lie, demand for Asia Pacific trial sites is strong with almost half of the more than 27,000 clinical trials initiated in 2021 having sites in Asia Pacific.
The data shows almost 12,900 of the new trials had sites in Asia Pacific.
The report also noted that the Asia Pacific region, which has more than 6,772 trial sites each with access to an average of 2,136 million people, has considerable underutilized capacity presenting an opportunity for growth in multinational trials in the region.
Novotech this month was awarded the Frost & Sullivan Company of the Year Award 2022 for Best Practices in the Asia-Pacific contract research organization industry. Novotech has been a recipient of the Frost & Sullivan Asia Pacific Best Practices awards since 2006.
Frost & Sullivan said:
“Our approach involves the deployment of best practices and strategic analytics across a value chain. Against this backdrop, Frost & Sullivan recognizes Novotech for its valuable achievement.
Novotech addresses the global drug development market’s unmet needs with a strong leadership focus that incorporates client-centric strategies with best-practice implementation.
From feasibility assessments to regulatory submission support, data management, medical monitoring, and project management, the company provides a 360-degree approach to drug development for its biotech clients.”
Novotech also recently produced a new publication for biotechs considering China for their clinical research, and the relevant processes required for global regulatory approvals.
The report details regulatory requirements for biotechs including NDA and IND processes as well as ex-US research guidance for a successful US FDA approval pathway.
Novotech provides the relevant regulatory knowledge and drug development pathways specifically designed to support the US FDA approval process, avoiding delays and additional costs.
Novotech has also recently been benchmarked as a top 10 CRO among the world’s leading CROs, is a finalist in the prestigious Scrip awards, and has just been awarded the Gene & Cell Therapy Excellence Award.
데이빗 제임스 (David James)
노보텍은 글로벌 실행 능력을 갖춘 아시아 태평양 중심의 선도적인 바이오텍 CRO 기업으로 국제적으로 인정받고 있습니다.
노보텍은 연구소, 임상1상 시험 기관, 약물 개발 컨설팅 서비스(DDC, Drug Development Consulting) 그리고 FDA 규제 전문성을 갖춘 임상 CRO 기업으로 1상에서부터 4상까지의 임상시험과 생물학적 동등성 시험을 포함하여 5,000건 이상의 임상 프로젝트에 참여한 경험이 있습니다. 노보텍은 아시아 태평양, 미국, 유럽에서 임상시험을 수행하고자 하는 바이오텍 고객들에게 서비스를 제공할 수 있습니다. 노보텍은 전 세계적으로 3,000명 이상의 직원과 34개의 사무실을 보유하고 있습니다.
보다 자세한 내용은 https://novotech-cro.com/contact를 통해 확인하실 수 있습니다.