While regulators have become more flexible about clinical trial design and the speed at which trials are conducted, the process is still complicated. The decentralization, diversification and acceleration of these trials puts greater pressure on all participants in the ecosystem to collaborate efficiently. This is particularly challenging for companies in the startup phase and small to midsize range who may lack much of the bandwidth and funding needed. It doesn’t have to be that way, and evidence shows it. In this short eBook, we’ll share how you can drive speed to market with more efficient clinical trials, using the SAS® Life Science Analytics Framework, a fully comprehensive platform that fulfills all the requirements of the FDA and is used by hundreds of customers across the life science industry.