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.
Including Women of Childbearing Age in Clinical Research
March 26th 2024In recognition of International Women's Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and Marie Teil, Global Head of UCB’s Women of Childbearing Age Program. They speak about the specific challenges women with chronic illnesses face when accessing appropriate treatment and participating in clinical trials, UCB's Women of Childbearing Age Program and it’s most successful strategies, and much more.
Regulatory Compliance With eCOAs
April 26th 2024In the fourth and final part of this video interview with ACT editor Andy Studna, Melissa Mooney, director, eCOA sales engineering, IQVIA discusses how the regulatory stance on electronic clinical outcome assessments has changed over the years and what it could look like in the future.
Improving Engagement While Maintaining Data Integrity & Validity
March 19th 2024In recognition of Women's Health Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and uMotif's Chief Product Officer, Julia Lakeland, discuss new technologies improving patient engagement and reducing the emotional and logistical burdens of participation, ethical considerations that should be addressed when implementing those technologies, while ensuring patient privacy, and much more.
Using Patient Reported Outcomes in Dermatology Trials
April 25th 2024In part 3 of this video interview with ACT editor Andy Studna, Melissa Mooney, director, eCOA sales engineering, IQVIA sheds light on the unique challenges of dermatology trials and how clinical outcome assessments can be implemented in them.