Pharmaceutical Technology - Pharmaceutical Manufacturing & Development News & Research for Scientists

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PharmTech Europe
Using Model-Predictive Design in Solid-Dosage Manufacturing Processes
Models and modeling software gain a foothold in solid-dosage manufacturing process design.
Industry Perspectives: Achieving Solutions for the Challenge of Poorly Water-Soluble Drugs
A multifaceted approach is needed to resolve the myriad of challenges in developing oral formulations of poorly soluble drugs.
Elucidating Heterocyclic Chemistry in Pharmaceuticals
Researchers at the Scripps Research Institute advance heteorcylic chemistry trhough new reagents and reaction-tracking techniques.
Measuring Tablet Hardness: A Primer
Crushing, fracturing, and bending tests quantify hardness.
Report from Southeast Asia
A unique demographic and payer mix make ASEAN an increasingly attractive region.

Expert Interviews, Industry Trends, and more

USP Supply Chain Safety Videos
pharmtech corporate capabilities 2012
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Praise and Perils for Biotechnology Patent Policy
Risk-Mitigation Strategies in Drug Manufacturing for Emerging Markets
Quality Focus: Ensuring Raw Material Transparency
Advertising of Prescription Drugs  Keeping it Honest and Balanced
Key Ways for Ensuring Global Regulatory Compliance
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Industry Leaders: Q+A
Q&A with Roberto Darienzo, Halo Pharmaceutical
Roberto Darienzo, chief operating officer of Halo Pharmaceutical, describes strategic plans and industry trends.
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Events
June 29, 2013 - July 1, 2013
 		BIT's 4th Annual Global Congress of Catalysis - 2013
July 8, 2013 - July 11, 2013
 		Pharma Trials World Korea 2013
July 11, 2013
 		DCAT's Sharp Sourcing 2013
The Marketplace
Regulatory Corner
Standards & Regulations
Regulatory Convergence Sought for Global Pharma Market
Manufacturers work with international authorities to harmonize drug registration and supply-chain oversight.
Regulatory Roundup
FDA faces budget crunch; Supreme Court hears key cases
Should Regulation of Combination Products Become More Centralized in Europe?
While there are those who want combination products to be controlled by a centralized pharmaceutical-type approval system, the majority of the medical technology industry wants to retain a decentralized device-focused approach.
Fixed-Oil Excipient Monographs: Development of USP Fixed-Oil Reference Standards
This article summarizes the development and modernization of the United States Pharmacopeia-National Formulary (USP-NF) fixed-oil excipient monographs. This article contains bonus online-exclusive material.
Eric Langer Outsourcing Outlook Eric LangerOutsourcing's Modest Role as a Cost-Containment Strategy
Patricia Van Arnum Ingredients Insider Patricia Van ArnumIntellectual Property Battles in Solid-State Chemistry
Nathan Jessop Industry Insider Nathan Jessop Campaign Against Counterfeit Drugs Continues
Lynn Torbeck Statistical Solutions Lynn D. TorbeckCompositing Samples and the Risk to Product Quality
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