Despite incredible advances in science and technology over the last decade, modern drug development remains a complex and costly process. With development costs of over $2.6 billion to bring a drug to market, new solutions need to be found. Clinical data standards can play a key role in improving the efficiency and quality of healthcare.
The life sciences industry is constantly challenged with integrating clinical data, reducing time to market, increasing drug development costs and adhering to stringent regulatory standards requirements. Data standardization can enable information system interoperability that improves medical research with the ultimate goal of creating regulatory submissions that are easily interpreted, understood and navigated by regulatory reviewers. Data standardization is both a regulatory requirement and a business opportunity.
How Can Navitas Help?
With deep experience and expertise in Clinical Data Solutions, our experts can provide solutions or utilize technology partnerships and provide the services you need to effectively implement them. In addition, we work with International Standards organizations such as CDISC to guide the creation of future standards. Being a technology-enabled service provider, we provide skilled professionals, build team across all therapeutic areas and play a pivotal role in enhancing data standards and system interoperability, thus improving the overall efficiency and quality of data.