On December 18, 2016, numerous regulatory agencies will require electronic submission of non-clinical data using CDISC’s standard format. What exactly are CDISC data standards and how will they impact drug developers? In this blog post, I will provide an overview of the CDISC SEND data standard, review some of the requirements for implementing SEND, and […]Read More
Author: Chris Lovejoy
Chris Lovejoy has been with Certara for over 16 years. Originally qualifying as a Pharmacist, his experience in the Pharmaceutical Industry includes PK/PD analysis, Drug Safety and Clinical Data Management. Based in the UK, Chris has been in involved in all the major European deployments of Phoenix solutions, acting as a technical and project management lead.