October 24, 2018 - October 25, 2018
New York, NY (USA)
October 24, 2018: 4:25 PM – 5:05 PM
Streamlining Database Set-up through use of Standards
PAREXEL is a leading global biopharmaceutical services organization with 30+ years assisting clients in the pharmaceutical, biotechnology, and medical device industries. We simplify the journey between science and new treatments through innovation and problem-solving. We help our clients determine the viability and value of their pharmaceutical, biotechnology and medical device products to create a healthier world. PAREXEL’s Metadata Repository (MDR) is designed utilizing a hub and spoke model bridging all cracks between different department standards. PAREXEL has developed a highly automated workflow and validation from the MDR into Rave Architect. By utilizing the MDR, study teams are able to see the positive impact of building from standards and the impact it has on study timelines and the quality of the database being delivered.
Speaker: Emma Thraves, Senior Manager, Clinical Database Programing
October 25, 2018: 10:30 AM – 11:10 AM
Fast Track Your Clinical Development Lifecycle
According to a recent industry survey, 80% of respondents agreed that Early Phase studies are becoming more complex. To compete, sponsors are under pressure to contain costs and timelines, while addressing increasingly demanding study requirements. We have assembled an expert panel to help you understand the trends, the impacts of these trends and what steps you can take to address these new challenges.
Speaker: Kenneth Lima, Senior Director, Data Management