Articles by Jennifer Markarian - Pharmaceutical Technology

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Articles by Jennifer Markarian

Using Robotics In Pharmaceutical Manufacturing

Robots are proving advantageous in filling, inspection, packaging, laboratories, and the manufacture of personalized medicine.
Nov 19, 2014

Robots are proving advantageous in filling, inspection, packaging, laboratories, and the manufacture of personalized medicine.

Process validation for continuous manufacturing processes

Nov 2, 2014

Although some aspects of process validation for continuous processes are the same as those for traditional batch processes, there are some unique considerations.

Continuous Solid-Dosage Manufacturing Platform Nears Prototype Installation

A G-CON, GEA, and Pfizer collaboration developed a PCMM (portable, continuous, miniature, and modular) system to produce oral solid-dosage drugs.
Nov 2, 2014

A G-CON, GEA, and Pfizer collaboration developed a PCMM (portable, continuous, miniature, and modular) system to produce oral solid-dosage drugs.

Evaluating Cross-Contamination Risk of Highly Potent APIs

Manufacturers using highly potent APIs must examine cross-contamination routes and determine acceptable limits.
Oct 15, 2014

Manufacturers using highly potent APIs must examine cross-contamination routes and determine acceptable limits.

Need for Particle Engineering Increases

Micronization and other processes are used to obtain optimal particle characteristics for pulmonary and oral solid-dosage delivery.
Sep 17, 2014

Micronization and other processes are used to obtain optimal particle characteristics for pulmonary and oral solid-dosage delivery.

Modularity Creates Flexible Manufacturing Systems

A roundtable discussion on modular bio/pharmaceutical manufacturing systems to enhance flexibility in facility design.
Sep 2, 2014

Flexibility, which involves the ability to quickly change product capacity or even product type to meet market demand, is increasingly important. In new construction or renovation, modular process skids and modular buildings create this flexibility. Experts discuss trends and challenges.

Preparing to Meet Counterfeiting Regulations

Sep 1, 2014

An expert discusses how companies should be preparing to meet the requirements of the Drug Supply Chain Security Act, which requires phase-in of requirements to prevent counterfeiting.

Lean Manufacturing Improves Process Efficiency

Manufacturers can identify and reduce waste using tools such as value-stream mapping.
Aug 20, 2014

Manufacturers can identify and reduce waste using tools such as value-stream mapping.

Implementing Supply-Chain Security

Companies in the US drug supply chain should prepare for the coming requirements of the Drug Supply Chain Security Act.
Aug 2, 2014

The US federal Drug Quality and Security Act (DQSA) and more specifically the Drug Supply Chain Security Act (DSCSA), referring to Title II of the law, requires phase-in of requirements to prevent counterfeiting. An expert discusses how companies should be preparing to meet the requirements of the DSCSA.

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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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