Displaying 1–25 of 309 results for USP

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Making the case for Indian generic drug manufacturing

(Article)

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.

Product Focus: Optimizing your ebb and flow

(Article)

New approaches to fluid control enhance pharma manufacturing

Retrofitting batch with single-use

(Article)

Automation & Control: Single-use technologies offer multiple benefits for those who can overcome instrumentation challenges.

Product Focus: The drug delivery link

(Article)

Innovations in materials and components play a critical role in protecting product quality

Optimizing precision blending of tablets

(Article)

Tumble blender technology can enhance the speed and homogeneous blending of tablets and capsules with trace levels of additives

The MLCM Paradigm Shift

(Article)

Quality & Compliance: Analytical methods based on performance are quickly becoming a compliance expectation.

QbD and Drug Packaging and Delivery: A Guide to Creating Safer Components

(Article)

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.

Analyzing for Elemental Impurities

(Article)

Understanding new guidance from the USP so that you can determine which approach to adopt when performing elemental impurity analysis.

Unpacking the Complexity of Biologic Drug Containment

(Article)

Thinking differently about material selection and system integration for biologics

2018 Pharma Innovation Awards

(Article)

A much-deserved celebration of manufacturing technologies, hand-picked by Pharmaceutical Manufacturing

Product Focus: Environmental Controls

(Article)

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.

Henry Ford Had It Right

(Article)

Hand-made to assembly lines, now, to automated production

Leaders of the Pack

(Article)

How contract packagers are accelerating pharma packaging innovation.

Cleanroom System Components: How To Select a Pass-Thru Airlock

(Article)

How To Select a Pass-Thru Airlock for your cleanroom system.

Drug Stability Testing and Analytics

(Article)

New challenges signify the need for a more unified biopharmaceutical industry

Malema Sensors SumoFlo Single-Use Flowmeters

(Product)

Malema Sensors SumoFlo Single-Use Flowmeters

Hospira Voluntarily Recalls Numerous Lots of Injectables

(News)

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.

WMFTG Quantum Peristaltic Pump for Single-use Downstream Bioprocessing

(Product)

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 Becomes ANSI Accredited Standards Developer

(News)

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

Investment in Biopharma Facilities Continues

(Article)

Many new facilities are designed for flexibility, combined with low-cost, highly efficient manufacturing

EpiPen Competitor Coming Soon from Kaleo

(News)

AUVI-Q (epinephrine injection, USP) auto-injector will enter the U.S. market in the first half of 2017

Mylan to Launch Generic to EpiPen At Half the Cost

(News)

Although still not inexpensive, Mylan will offer a generic to its EpiPen Auto-Injector at a list price of $300 per two-pack carton

Q&A: Pharma's Evolving Packaging Systems

(Article)

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.

Key Elements to Consider When Packaging Parenteral Products

(Article)

With a complete understanding of processes and test methods, sub-visible particles and bacterial endotoxins can be reduced to acceptable levels.

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