Displaying 1–25 of 156 results for USP
In response to the growing regulatory environment, pharmaceutical companies in India continue to strengthen their processes, while improving automation, operating procedures and quality management systems.
New approaches to fluid control enhance pharma manufacturing
Automation & Control: Single-use technologies offer multiple benefits for those who can overcome instrumentation challenges.
Innovations in materials and components play a critical role in protecting product quality
Tumble blender technology can enhance the speed and homogeneous blending of tablets and capsules with trace levels of additives
Quality & Compliance: Analytical methods based on performance are quickly becoming a compliance expectation.
The increase in injectable biologic and biosimilar treatments is requiring a stronger focus on quality requirements with respect to how the drugs are packaged and delivered.
Understanding new guidance from the USP so that you can determine which approach to adopt when performing elemental impurity analysis.
Thinking differently about material selection and system integration for biologics
A much-deserved celebration of manufacturing technologies, hand-picked by Pharmaceutical Manufacturing
Product Focus: Environmental Controls -- Pharma manufacturers must optimize their operations and controls — while adhering to strict regulatory guidelines — in order to maintain quality and increase efficiency.
Hand-made to assembly lines, now, to automated production
How contract packagers are accelerating pharma packaging innovation.
How To Select a Pass-Thru Airlock for your cleanroom system.
New challenges signify the need for a more unified biopharmaceutical industry
Many new facilities are designed for flexibility, combined with low-cost, highly efficient manufacturing
With Pharma EXPO just two months away, Pharmaceutical Manufacturing discusses the challenges of today's quickly changing packaging systems with Jerry Martin, pharmaceutical and life sciences consultant to PMMI, The Association of Packaging and Processing Technologies.
With a complete understanding of processes and test methods, sub-visible particles and bacterial endotoxins can be reduced to acceptable levels.
Well-known shortcomings of customary, online weight measurements systems are discussed, especially for industrial applications in the pharmaceutical industry.
New techniques are expanding the role of X-ray analytical technologies to range from drug discovery to quality control
In-process testing for contaminants is only as good as the methods used, so employing carefully developed and validated protocols is essential
Parenteral drug manufacturers are sharpening capabilities and coming into their own
International Conference on Harmonization represents the countries interested in unified standards
Misdirection in the implementation of isolation technology
The complexity of biologics makes it imperative to consider some tough questions that need asking when seeking a more specialized large molecule CMO.