Int. Journal of Drug cGMP
USA Edition

Locum International Press.

Issues #1 - # 8
Eight issues /year.

The International Journal of Drug cGMP - US Edition is targeted to the US geographic zones (Firms who require to understand current US GMP).

When the FDA knocks on your door for a GMP or PAI inspection - you will be glad you subscribed. Learn about the problems and prospects in the regulatory environment and receive practical advise on compliance from top industry experts.

The journal publishes articles, reviews and papers on all aspects of Generic and Innovative Drug cGMP. Emphasis is places on current Good Clinical, Development, Validation, Manufacture, Laboratory and Documentation Practices.

The US Journal highlights cGMP exposure of the Drug Industry with special reference to the on-time development of NDA and ANDA submissions. Similar concepts are valid for the EU and PR editions.

All aspects of pharmaceutical Good Practices covering practical hands-on nuts-and- bolts issues that vary across the full drug spectrum, including excipients development (pre-to-final) formulation, scale-up, analytical, cleaning and process validation necessary for the entire drug manufacture and control process to meet the agencies expectations.

The overall objective in cGMP is to maintain the current drug profile in the market place avoiding warning letters and negative PAI inspections.
The Journal attempts to clarify and simplify laboratory, manufacturing and control GMP, GLP, GDP, GVP and GRP issues to achieve this crucial objective.

80 - 95 pp illustrated b/w & color
Subscription Option Availability Print/CD/PDF via e-mail/Online

$1299.00 - Print Edition (single-user airmail print edition worldwide)
$1699.00 - Corporate single license single pharma campus - (Print / CD)
$1999.00 - Corporate multiple-user license - (print + CD edition maximizes distribution and readership for multiple pharma campus).

USA volume starts annually in March - Euro in June & Pacific Rim in September..

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