The authors offer recommendations for permissible daily exposures and concentration limits of elemental impurities for dermal drug products.
The authors offer recommendations for permissible daily exposures and concentration limits of elemental impurities for dermal drug products.
The authors offer recommendations for permissible daily exposures and concentration limits of elemental impurities for dermal drug products.
The authors offer recommendations for permissible daily exposures and concentration limits of elemental impurities for dermal drug products.
The authors offer recommendations for permissible daily exposures and concentration limits of elemental impurities for dermal drug products.
Particulate modelling has the potential to transform productivity within the pharmaceutical manufacturing industry, speeding up production cycles, reducing manufacturing costs, improving efficiency, and driving inward investment, with the potential to reinstate the UK as a global manufacturing powerhouse.
A new algorithm uses a statistical approach to critical process parameter assessment, allowing for faster, more consistent, and less subjective critical process parameter quantification, visualization, and documentation.
A new algorithm uses a statistical approach to critical process parameter assessment, allowing for faster, more consistent, and less subjective critical process parameter quantification, visualization, and documentation.
A new algorithm uses a statistical approach to critical process parameter assessment, allowing for faster, more consistent, and less subjective critical process parameter quantification, visualization, and documentation.
A new algorithm uses a statistical approach to critical process parameter assessment, allowing for faster, more consistent, and less subjective critical process parameter quantification, visualization, and documentation.
A new algorithm uses a statistical approach to critical process parameter assessment, allowing for faster, more consistent, and less subjective critical process parameter quantification, visualization, and documentation.
A new algorithm uses a statistical approach to critical process parameter assessment, allowing for faster, more consistent, and less subjective critical process parameter quantification, visualization, and documentation.
SCHOTT is integrating a specially developed big data solution into its pharmaceutical tubing production, replacing statistical sample-based quality assurance with 100 percent on-line measurement.
Chemspec Europe will take place from 26 – 27 June 2019 at Messe Basel in Switzerland.
-Research suggests cyclodextrins could replace surfactants for biologics. -Studies on HPßCD indicate it to be a potential alternative to polysorbates.
Umicore Precious Metals Chemistry offers a collaborative approach to research, development and commercial manufacturing of your complex organometallic chemistry and catalysis needs.
Grifols Partnership is a business-to-business contract development and manufacturing platform for sterile solutions and lipid emulsions with a long-term experience in producing intravenous solutions for the pharmaceutical industry worldwide.
The need for real-time monitoring and control has spurred the development of new analytical tools.
A systematic framework and software are needed to implement material traceability in continuous pharmaceutical tablet manufacturing.
The increase in aseptic processing driven by the growing number of biologically-derived products has led to an increase in freeze-drying applications in this area at both research and production scales.
The following study describes a methodology to establish, control, and characterize an aerosolized bioburden within a test chamber and determine the settling rate of the bioburden.
The following study describes a methodology to establish, control, and characterize an aerosolized bioburden within a test chamber and determine the settling rate of the bioburden.