For Organic sample processing while in the manufacture of therapeutic proteins or cell and gene therapies, to circumvent downstream contamination
Endotoxins are heat secure and persist even just after bacterial death. Their inactivation is neither doable with boiling nor with autoclaving. On the
A glass cuvette is just not ideal for UV spectroscopy as it absorbs UV light-weight, that may interfere Along with the measurement becoming taken. Quartz cuvettes are typically employed for UV spectroscopy because they are transparent to UV light-weight and do not take up it.
UV-Vis spectroscopy,
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Analytical validation is meant to verify that the chosen analytical strategy is effective at delivering trustworthy effects which have been suitabl
Exactly what are the Agency’s recommendations about in-procedure stratified sampling of concluded dosage units?
This may appear daunting – prolonged terms and sophisticated sentences generally have that impact – but it doesn’t must be.
The target of FDA's PAT progra
Information-supported, management-authorised, and last cleaning validation report stating whether the cleaning approach for a certain piece of equipment or producing process is legitimate
Pharmaguideline is actually a pharmaceutical weblog in which pharmaceutical principles are stated in quite si