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Pharm Tech
October 2016
Volume 28, No. 10
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| COVER STORY |

Keeping the Drug Supply Safe

Agnes Shanley

As criminals duplicate the latest overt security technologies, pharmaceutical manufacturers are evaluating covert and layered approaches to fight counterfeiting, theft, and illegal product diversion.
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Tracking a Global Problem

Agnes Shanley

A number of organizations have analyzed and estimated the size of pharma's counterfeit and diversion problem.
/ read more /


| EXCIPIENTS |

Excipients for Formulation Success

Adeline Siew, PhD

Excipients play a crucial role in the manufacturing of solid-dosage forms and the performance of the finished drug product.
/ read more /

| FORMULATION |

Reverse Engineering a Pressurized Metered Dose Inhaler

Sarah Dexter, Alex Slowey

Understanding the components of a reference marketed pMDI is needed to develop a generic pMDI.
/ read more /

PharmTech Europe October Issue
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| PEER-REVIEWED RESEARCH |

Impact of Quality by Design on Topical Product Excipient Suppliers, Part I: A Drug Manufacturer's Perspective

David W. Osborne

This article will equip the excipient vendor with an understanding of QbD from the perspective of the topical pharmaceutical product manufacturer.
/ read more /


| OUTSOURCING |

Fill/Finish Outsourcing

Eric S. Langer

This key bioprocessing segment is expecting continued growth.
/ read more /


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| REGULATORY WATCH |

Pharmacovigilance of Biologics Under Scrutiny

Sean Milmo

Regulators are tightening up on post-marketing monitoring of biological medicines to detect deficiencies caused by manufacturing problems, particularly those stemming from post-authorization changes in the manufacturing process.
/ read more /


| API SYNTHESIS & MANUFACTURING |

The Search for Practical and Economical Catalysts

Cynthia A. Challener

Researchers develop catalysts that mediate complex transformations under conditions appropriate for commercial manufacture.
/ read more /


| PACKAGING FORUM |

Protecting Parenterals in Primary Packaging

Hallie Forcinio

Primary packaging and manufacturing technologies minimize product/package interaction, protect quality, support safe travel through the supply chain, and enhance performance at point of use.
/ read more /


| TROUBLESHOOTING |

Improving Feeder Performance in Continuous Pharmaceutical Operations

Sharon Nowak

Designing loss-in-weight feeders for accurate and consistent refill is crucial to a continuous solid-dosage process.
/ read more /


| ASK THE EXPERT |

Defining Risk Assessment of Aseptic Processes

Susan J. Schniepp

Susan Schniepp, distinguished fellow at Regulatory Compliance Associates, discusses the assessment of risk in the processing of intravenous injectable drugs.
/ read more /


| EVENTS |

PDA Visual Inspection Forum

25-26 October, 2016 | Berlin, Germany

BIO Europe

7-9 November, 2016 | Cologne, Germany

3rd Annual Computer System Validation Workshop

8-9 November, 2016

more events
 
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