Innovations in the pharmaceutical industry, particularly in the areas of patient clinical testing and drug manufacturing, have significantly shortened the time needed to bring new drugs to the market. Because these new processes are more efficient, this means ensuring quality throughout the clinical trial and manufacturing stages is more important than ever.
Download our insight brief to learn why a robust risk management program is essential for ensuring quality in pharmaceuticals during development and manufacturing.
Download this insight brief to learn more about:
- The advancements in pharmaceutical trials and manufacturing that drive quality management
- How Quality by Design (QbD) principles build quality into both clinical trials and the manufacturing process
- Why integrating EHS, quality, and risk management is key to driving operational performance in pharmaceuticals