Articles by Rita Peters - Pharmaceutical Technology

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Articles by Rita Peters

Hype vs. Health

Nov 2, 2014

Ebola Virus Disease (EVD) is a severe, often fatal disease that is transmitted human-to-human through bodily fluids.

API Developers Note Upgrades, Successful Inspections

Added manufacturing capabilities, partnerships, and regulatory milestones mark recent achievements by API developers.
Sep 29, 2014

Added manufacturing capabilities, partnerships, and regulatory milestones mark recent achievements by API developers.

Excipient Variability: Causes, Identification, Control

Sep 29, 2014

Industry experts examine reasons why the quality and composition of excipients can vary including environmental factors, processing methods, raw material quality, manufacturing location changes, and operator actions.

Meeting the Challenges of Excipient Variability

Sep 1, 2014

The quality and composition of excipients can vary due to environmental factors, processing methods, raw material quality, manufacturing location changes, and even operator actions.

API Developers Pass Inspections and Upgrade Capabilities

API development and manufacturing companies expanded their capabilities, built partnerships, and achieved milestones in regulatory inspections.
Sep 1, 2014

API development and manufacturing companies expanded their capabilities, built partnerships, and achieved milestones in regulatory inspections.

Contract Providers Assume Expanded Responsibilities

Sep 1, 2014

Contract service providers are playing a more diverse role in drug development.

A Silver Milestone for Drug Development

Pharmaceutical Technology Europe marks 25 years of drug-development advances.
Aug 2, 2014

Pharmaceutical Technology Europe marks 25 years of drug-development advances.

Shifting Gears in Drug Development Outsourcing Responsibilities

Aug 1, 2014

For a bio/pharma industry in flux, contract services are playing a greater—and more diverse—role in drug development.

Benefits and Risks of Drug Information on Social Media

Jul 2, 2014

FDA draft guidances seek to maintain accurate drug information for patients in new media.

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Jill Wechsler Regulatory Watch Jill Wechsler New Era for Generic Drugs
Sean Milmo European Regulatory WatchSean MilmoTackling Drug Shortages
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