Tokyo-based Asklep joins Medidata partner programme to expand clinical trial services
Asklep has joined the Medidata Solutions Partner Programme to increase the quality and efficiency of clinical trials.
Asklep, a leading provider of clinical research services based in Tokyo, has announced its decision to join the Medidata Solutions Partner Programme.
The move is part of the company's strategy to expand its clinical trial services in the Asia Pacific region and support its sponsors more effectively.
It will use the Medidata platform to increase the quality and efficiency of its clinical trials and post-marketing studies, helping to streamline key areas of the clinical trials process for its customers.
By seeking several accreditations across Medidata's cloud-based platform, Asklep will benefit from being able to offer a variety of on-demand resources, including electronic data capture and clinical data management.
Masahito Ikeda, corporate officer and deputy division director of clinical information at the company, said: "It's critical that our partners share our mission and dedication to improving the clinical trial process for research sponsors.
"We've been impressed with Medidata's track record streamlining global trials of all sizes and phases and the strong preference among sites to use the Medidata platform for electronic patient data capture."
Tarek Sherif, chief executive officer of Medidata Solutions, added that Asklep joins a growing community of partners that use the company's cloud-based platform to improve productivity and reduce costs.
Related News
-
News Understanding the Benefits and Advances of Cleanroom Technology
In an industry where precision and sterility are crucial concerns, cleanrooms play a vital role in maintaining the integrity of pharmaceutical products like drugs, vaccines, and other medical products. So, what is a cleanroom?
-
News AbbVie secures GBP£1.2 billion deal for Gilgamesh’s psychedelic programme
AbbVie has penned a significant agreement to acquire the bretisilocin programme from Gilgamesh Pharmaceuticals for up to £1.2 billion, marking a bold step in the pharmaceutical giant's quest to develop treatments for psychiatric disorders. -
News Gates Foundation commits US$2.5 billion to women’s health research
The Bill & Melinda Gates Foundation has announced a substantial US$2.5 billion commitment to accelerate research and development focused exclusively on women's health through 2030.
-
News Mid-year review: notable FDA drug approvals of 2025
As we fly past the halfway point of 2025, the pharmaceutical landscape reliably continues to evolve with innovative therapies addressing critical medical needs. The FDA has already approved 17 groundbreaking medications this year, each representin... -
News US FDA announces new priority vouchers for accelerated review times
The US FDA announced a new priority program for drug developers – the Commissioner’s National Priority Voucher (CNPV) program aims to enhance the health interests of the US by allowing drug developers to redeem a voucher, shortening th... -
News Google-backed start-up raises US$600 million to support AI drug discovery and design
London-based Isomorphic Labs, an AI-driven drug design and development start-up backed by Google’s AI research lab DeepMind, has raised US$600 million in its first external funding round by Thrive Capital. The funding will provide further power t... -
News AstraZeneca to invest US$2.5 billion in Beijing R&D centre
Amid investigations of former AstraZeneca China head Leon Wang in 2024, AstraZeneca have outlined plans to establish its sixth global strategic R&D centre in China. Their aim is to further advance life sciences in China with major research and manufact... -
News Experimental drug for managing aortic valve stenosis shows promise
The new small molecule drug ataciguat is garnering attention for its potential to manage aortic valve stenosis, which may prevent the need for surgery and significantly improve patient experience.