Displaying 1–25 of 309 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
Malema Sensors SumoFlo Single-Use Flowmeters
Questions about product sterility due to microbial growth have caused Pfizer's Hospira to issue a large recall of various injectables distributed from January to June 2017.
The product aims to introduce a flow linearity with lowest pulse, a wide turndown with ultra-low shear, a simple to use single-use technology and easier validation.
PDA has been approved by ANSI to be an ASD because PDA’s portfolio of technical reports includes many topics that are good candidates to become American National Standards
Many new facilities are designed for flexibility, combined with low-cost, highly efficient manufacturing
AUVI-Q (epinephrine injection, USP) auto-injector will enter the U.S. market in the first half of 2017
Although still not inexpensive, Mylan will offer a generic to its EpiPen Auto-Injector at a list price of $300 per two-pack carton
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.