Why This Conference?
The current competitive and global clinical trial environment is facing new challenges for IP material management, particularly in regard to the interactions with regulatory bodies.
Keeping up with new Clinical Trial and GDP regulations and the developing technologies, systems and processes is the key to ensuring compliance and avoiding costly production delays.
Understand how the experience of participating patients impacts the success of any clinical trial and should have a bigger impact on GMP decisions on clinical materials. Attend this conference to gain first-hand insights and knowledge resulting from the ISPE Patient Survey.
REGISTER NOW » - Early Bird ends 22 August!