
USP’s Sheehan and Liu talk at AAPS PharmSci 360 abou getting novel excipients past the monograph hurdle through early engagement with FDA.
In a market where high-demand causes organizations to seek software systems that will fit into their complex business infrastructure, the pressure to find the right system often causes angst to many.
Learn some key elements to spotting a good FDA Compliance solution, techniques for achieving Good Manufacturing Practice (GMP) Compliance, and how to ensure that Quality and Compliance are met in the Life Science industry.






