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USP Reference Standards & Pharmaceutical Analytical Impurities

USP Reference Standards & Pharmaceutical Analytical Impurities For over 200 years USP (United States Pharmacopoeia) has worked to build trust where it matters most in the world's medicines dietary supplements and foods. Contact your specialist Hel...

The Meaning of ‘Clean’: Mitigating the Risk of Particulate Contamination from Single-Use Technologies

The Meaning of ‘Clean’: Mitigating the Risk of Particulate Contamination from Single-Use Technologies Webinar Tuesday 6th October 2020 17:00 to 18:00 CEST (Berlin Paris Madrid) PRESENTED IN ENGLISH Replay Email Alerts Free Registration Chat Area C...

Disinfectant efficacy validation for life science cleanrooms

Disinfectant efficacy validation for life science cleanrooms Webinar Thursday 22nd July 2021 11:00 to 12:00 CEST (Berlin Paris Madrid) Replay Email Alerts Free Registration Chat Area Certificate of attendance Understand the differences in disinfec...

Buffer management solutions

Buffer management solutions Buffers play a significant role in biopharmaceutical manufacturing. Typically representing a major component by volume used in downstream processing steps buffer preparation constitutes a significant proportion of a fac...

Optimizing your buffer, reagent and culture media management across biopharma workflows

Optimizing your buffer reagent and culture media management across biopharma workflows The adoption of hydrated premade liquid buffers reagents and cell culture media can save you time resources and money. Different strategies for solutions prepar...

Optimizing your buffer, reagent and culture media management across biopharma workflows

Optimizing your buffer, reagent and culture media management across biopharma workflows The adoption of hydrated, premade liquid, buffers, reagents and cell culture media can save you time, resources and money. Different strategies for solutions p...