Guidelines for Authors - Pharmaceutical Technology

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PharmTech

Latest Issue
PharmTech Europe

Guidelines for Authors
Jan 1, 2012
Pharmaceutical Technology

Pharmaceutical Technology and Pharmaceutical Technology Europe magazines welcome manuscripts on subjects pertinent to all aspects of drug development. See the following PDFs for more information on article contributions.

Pharmaceutical Technology North America

Guidelines for Authors

Guidelines for Supplements

Guidelines for Sourcing and Management eNewsletter

Please see our media kit for the 2012 editorial calendar.

Pharmaceutical Technology Europe

Guidelines for Authors

Editorial Calendar

Pharm Tech Talk

We also welcome contributed posts on our blog, PharmTech Talk, and encourage readers to leave comments. For information on blogging for PharmTech Talk, contact Angie Drakulich, the Editorial Director.

If you have any questions, please Contact Editorial.

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Survey
Looking forward 10 years from now, what do you think will be the most significant change to drug development and manufacturing?
Fuller adoption of quality by design principles
Greater adoption of continuous manufacturing
A stronger movement to personalized medicine and the use of diagnostics with traditional pharmaceuticals
The rise of biologic-based drugs in commercial product portfolios and pipelines
Greater adoption of the preferred provider model in outsourcing
Fuller adoption of quality by design principles
22%
Greater adoption of continuous manufacturing
7%
A stronger movement to personalized medicine and the use of diagnostics with traditional pharmaceuticals
35%
The rise of biologic-based drugs in commercial product portfolios and pipelines
30%
Greater adoption of the preferred provider model in outsourcing
7%
View Results
Jim MillerOutsourcing OutlookJim Miller Channeling Steve Jobs
Patricia Van ArnumIngredients InsiderPatricia Van ArnumSeeking Chemocatalytic and Biocatalytic Solutions
Nathan JessopIndustry InsiderNathan Jessop Taxing Times for French Pharma
Lynn D. TorbeckStatistical Solutions Lynn D. TorbeckRepresentative Sampling
Report on Recent and Upcoming Single-Use Meetings
ICH Q11 Reaches Harmonization, Implementation is Next
Digital Signatures Growing as a Result of Part 11
Single-Cell Genomics Advancing Molecular Biology
Putting FDA’s “Process Validation” Guidance into Action

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