PRA Expands Operations in China, New Beijing Office to Strengthen Regional Service
PRA, a leading Clinical Research Organization, announces the opening of a second office in China to accommodate its continued expansion in China and the Asia Pacific region. PRA established its first China office in Shanghai in 2005. PRA’s new facility, located in the central business district of Beijing, is designed to enhance the company's local project teams’ ability to meet the growing demand for clinical drug development programs and co-locate with key clients in Beijing.
“As the demand for clinical sites in Asia increase, we continually strive to strengthen our existing operations in China and the Asia Pacific region,” said Helen Neal, Regional Director – Clinical Operations, Asia Pacific, Middle East, and North Africa. “By adding more professional staff and locations, we can give our clients greater access to these critical markets and geography. In addition to our expansion in China, we continue to increase our presence into new and emerging Southeast Asian regions for access to patients and resources.”
“We are very excited about our continued expansion into China,” said Kent Thoelke, Executive Vice President, Scientific & Medical Affairs. “In order for global drug development to continue successfully, the need to access patients at high-quality ICH/GCP sites in emerging regions like China is critical. PRA’s expansion in this market gives us the ability to bring exciting new clinical trials to a much broader market in China, while providing even greater patient access to our clients and sponsor companies.”
PRA has been operating in China for over 10 years and also has an office in Hong Kong. Additional Asia Pacific locations include South Korea, Taiwan, Thailand, Singapore, Australia, New Zealand, and India.
Improving Relationships and Diversifying the Site Selection Process
April 17th 2025In this episode of the Applied Clinical Trials Podcast, Liz Beatty, co-founder and chief strategy officer, Inato, discusses a number of topics around site engagement including community-based sites, the role of technology in improving site/sponsor relationships, how increased operational costs are impacting the industry, and more.
Behind the Buzz: Why Clinical Research Leaders Flock to SCOPE Summit
February 7th 2025In this episode, we meet with Micah Lieberman, Executive Conference Director for SCOPE Summit (Summit for Clinical Ops Executives) at Cambridge Innovation Institute. We will dive deep into the critical role of collaboration within the clinical research ecosystem. How do we bring together diverse stakeholders—sponsors, CROs, clinical trial tech innovators, suppliers, patients, sites, advocacy organizations, investors, and non-profits—to share best practices in trial design, program planning, innovation, and clinical operations? We’ll explore why it’s vital for thought leaders to step beyond their own organizations and learn from others, exchanging ideas that drive advancements in clinical research. Additionally, we’ll discuss the pivotal role of scientific conferences like SCOPE Summit in fostering these essential connections and collaborations, helping shape the future of clinical trials. Join us as we uncover how collective wisdom and cross-industry partnerships are transforming the landscape of clinical research.
