News & Analysis on Clinical Trial Services & Contract Research And Development
Setting the groundwork for successful scale-up is essential for getting a therapeutic to market quickly and efficiently, but navigating the unknowns associated with this process can be challenging. Beyond procurement challenges, raw materials need to undergo quality control (QC) testing prior to preparation for process liquids and buffers. The documentation, validation, and training associated with these processes also present challenges to facilities that must allocate...
A growing contract development manufacturing organization (CDMO) was challenged with the need to quickly expand their process liquid and buffer preparation capacity in order to meet the demand for one of their client’s recently approved therapeutic
Consider how the right partner can help you scale faster, mitigate risks, and optimize resources.
For more product information visit Thermo Fisher Scientific - Process Liquid Preparation Services.