The pressure to increase productivity in the pharmaceutical industry, whilst maintaining compliance and reducing costs, is relentless. This meeting will examine the role of technologies and continuous improvement techniques in optimising throughput, cycle times and allocation of resources in QC and stability testing laboratories, using expert perspectives and case studies from industry, regulatory agencies and partner organisations.
It is aimed at laboratory managers and pharmaceutical analysts striving to improve workflows leading to critical decisions and deadlines, as well as those new to the area seeking a broader understanding of the key scientific and operational issues. There will also be networking and exhibitor opportunities.
It is aimed at laboratory managers and pharmaceutical analysts striving to improve workflows leading to critical decisions and deadlines, as well as those new to the area seeking a broader understanding of the key scientific and operational issues. There will also be networking and exhibitor opportunities.
