Subscriptions - Pharmaceutical Technology

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PharmTech Europe

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Pharmaceutical Technology Magazine | Monthly
Authoritative, reliable and timely peer-reviewed research and expert analysis for scientists, engineers, technicians and managers engaged in process development, manufacturing, formulation, analytical technology, and regulatory compliance in the pharmaceutical and biotechnology industries.

US Subscribers | Subscribers Outside the US

Pharmaceutical Technology Europe | Monthly
The market-leading monthly publication for European professionals actively involved in all areas of pharmaceutical manufacturing. PTE magazine offers exclusive peer-reviewed research, interviews with industry experts and features on new technologies, product developments, regulatory issues and practical solutions to promote best practice in pharmaceutical manufacturing.

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PharmTech newsletters

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ePharmTechnology | Weekly
The latest in business, scientific and regulatory news shorts, plus upcoming events and career opportunities delivered to your inbox every Thursday.
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Sourcing & Management | Monthly
News and expert coverage of the supply chain with insights on sourcing of APIs, intermediates, and other ingredients – featuring technology management, outsourcing and pharmaceutical chemical development. Click here to view the Sourcing & Management Community of Experts.
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Equipment and Processing Report | Monthly
Focus on pharmaceutical manufacturing processes and technology, providing analysis of manufacturing news, related regulatory issues, and current trends. Each issue features a showcase of processing equipment and reviews, as well as upcoming events.
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Pharm Tech Europe E-Alert | Weekly
Providing important industry, regulatory, research and business news from Europe's pharmaceutical manufacturing sector, as well as upcoming events specially selected by the editorial team. Additional features include exclusive pharmaceutical technology articles and interviews from industry experts about the latest trends, products and innovative technological developments.
 

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Survey
FDASIA was signed into law two years ago. Where has the most progress been made in implementation?
Reducing drug shortages
Breakthrough designations
Protecting the supply chain
Expedited reviews of drug submissions
More stakeholder involvement
Reducing drug shortages
70%
Breakthrough designations
4%
Protecting the supply chain
17%
Expedited reviews of drug submissions
2%
More stakeholder involvement
7%
View Results
Eric Langerr Outsourcing Outlook Eric LangerTargeting Different Off-Shore Destinations
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerAsymmetric Synthesis Continues to Advance
Jill Wechsler Regulatory Watch Jill Wechsler Data Integrity Key to GMP Compliance
Sean Milmo European Regulatory WatchSean MilmoExtending the Scope of Pharmacovigilance Comes at a Price
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