As the industry demands a faster, more accurate approach to pharmacovigilance using new technologies, a recent study found that more than 60 percent of respondents are implementing artificial intelligence (AI) to improve adverse event processing.
The China Food and Drug Administration (CFDA) has been driving reforms to improve the quality of drugs and encourage innovation in the development of new drugs and medical devices. As with any new clinical trial, tremendous time and resources are required to set up a new study, including trial design and validation. Sichuan Kelun Pharmaceutical has automated their oncology clinical trial set up and management using Oracle Health Sciences Clinical One Randomization and Supplies Management.
We needed an established, standards-based cloud system to simplify the drug supply management process.
— Xiaoping Zhang, VP of Biostatistics and Data Management, Clinical Research Hub
Clinical One unifies every element of your clinical development world.
ClearTrial Plan and Source Cloud Service leverages embedded industry intelligence and clinical knowledge to optimize clinical study planning and sourcing.
The clinical trial process doesn’t need to be a lengthy, expensive ordeal. Find out how Oracle Health Sciences Clinical One Platform brings the efficiency and agility of the cloud to manage the entire clinical development lifecycle.