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Dust collector explosions are a danger in many industries, but the pharmaceutical industry is particularly at risk.
This white paper covers applications of MVA and DoE and illustrates how these powerful analytical tools can be integrated with different systems throughout a biotechnology operation for accelerated development, reduced process related costs and improved time to market.
This guide includes the top questions a trusted vacuum supplier will ask to assess your specific application and facility needs. It is designed as a resource to help jump-start your search for the right partner and the right industrial vacuum cleaner to get the job done.
Download your copy of this Pharmaceutical Manufacturing Special Report: Control Systems in Biopharma Applications now.
Learn more about eMDR.
This eBook contains trend articles that map the direction of the industry and expected near-term trends.
Learn how companies can move on from solubility when it comes to cleaning validation.
This App Note explains how to ensure continued GxP compliance in your monitoring system for temperature-controlled environments.
The Pharmaceutical Industry's Transition to Electronic Processes
How Effective Document Management Helps Pharmaceutical Companies Accelerate Time to Market
Managing your Risk Has Its Rewards: Making the Case for Risk Assessment in Streamlining your Quality and Compliance Processes
Accelerating Innovation for Competitive Advantage in Pharmaceutical Manufacturing
Six Corporate Oversights of Quality and Compliance Issues in Pharmaceutical Environments
Four Ways to Better Production Efficiency
Solutions Brief: Single-Use Pumps Meet Biopharmaceutical Scale-Up, Validation and Product Sensitivity Challenges
Total Organic Compound (TOC) Measurement
Thermistors and Thermocouples: Matching the Tool to the Task in Thermal Validation
Validation FAQs - Five Key Questions You Need to Have Answered in Planning a Validation Project