Sydney, Australia and Seoul, Korea - Asia Pacific specialist CRO Novotech announced today it has signed a Memorandum of Understanding (MOU) with South Korea’s largest medical institution – The Asan Medical Center’s (AMC) Clinical Trial Center. The MOU formalises Novotech’s relationship with the internationally-leading medical center and its principal investigators.
Under the terms of the MOU, the AMC will provide professional and medical advice to Novotech for clinical trials conducted in AMC; including feasibility, principal investigator selection and assistance with patient recruitment. Novotech will assist in promoting the clinical research capabilities of the AMC internationally. Both parties have agreed to continue expanding the future scope of the collaboration.
Speaking for the AMC, Director of Asan Medical Center’s Clinical Trial Center Dr. Young Suk Lim said "AMC has been very successful in delivering and supporting many complicated clinical trials, including early phase clinical trials. Based on the MOU, the AMC is committed to increasing and expanding its global-level of medical and technological infrastructure, and continuing to deliver quality clinical trial support.”
Commenting on the MOU, Novotech CEO Dr. John Moller said “The AMC and its Clinical Trial Center is a globally renowned medical institution. We have worked closely the AMC’s Clinical Trial Center on many clinical trials over our ten-year history in South Korea and we have been impressed with the quality of clinical support delivered by the Center.”
“AMC’s size, high quality facilities and technological infrastructure are crucial in delivering speedy patient recruitment, quality clinical trial management and robust trial data. AMC has over 2,700 beds and the volume of available patients is huge by Western standards. Other elements which contribute to South Korea being a leading destination for clinical trials include its efficient regulatory environment and its high standards of trial conduct,” added Dr. Moller, “Novotech looks forward to working with the AMC and offering the benefits of South Korea as a clinical trial destination to our clients.”
To hear more about the benefits of undertaking a clinical trial in South Korea with Novotech, please contact us via www.novotech-cro.com/contact-us-0About the Asan Medical Center
Since its establishment in June, 1989, ASAN Medical Center has achieved a world-class medical reputation as it has continued to aggressively invest in R&D and clinical treatment. AMC is leading medical development in Korea with their competitive skills and cutting-edge equipment comparable to those of advanced foreign hospitals. ASAN Medical Center is the parent hospital of eight hospitals under the ASAN Foundation. www.amc.seoul.kr/asan/lang.eng.aboutAMC.introduction.spAbout Novotech
Headquartered in Sydney, Novotech is internationally recognised as the leading regional full-service contract research organisation (CRO). With a focus on clinical monitoring, Novotech has been instrumental in the success of hundreds of Phase I - IV clinical trials in the Asia Pacific region.
Novotech provides clinical development services across all clinical trial phases and therapeutic areas including: feasibility assessments; ethics committee and regulatory submissions, data management, statistical analysis, medical monitoring, safety services, central lab services, report write-up to ICH requirements, project and vendor management. Novotech’s strong Asia Pacific presence included running clinical trials in all key regional markets. Novotech also has worldwide reach through the company's network of strategic partners. www.novotech-cro.com
Roche’s Susvimo Lands FDA Approval for Diabetic Retinopathy Based on Phase III Pavilion Trial Data
May 22nd 2025One-year results from the Pavilion study showed patients who received Susvimo (ranibizumab) refilled every nine months achieved superior improvements on the Diabetic Retinopathy Severity Scale.
Unifying Industry to Better Understand GCP Guidance
May 7th 2025In this episode of the Applied Clinical Trials Podcast, David Nickerson, head of clinical quality management at EMD Serono; and Arlene Lee, director of product management, data quality & risk management solutions at Medidata, discuss the newest ICH E6(R3) GCP guidelines as well as how TransCelerate and ACRO have partnered to help stakeholders better acclimate to these guidelines.
FDA Outlines Updated Requirement for Placebo-Controlled Trials in Vaccine Research
May 21st 2025In an article recently published by The New England Journal of Medicine, FDA higher-ups Vinay Prasad, MD, MPH; and Martin A. Makary, MD, MPH, wrote that any new COVID-19 vaccine must now be evaluated in placebo-controlled studies.