Cyco Software releases new pharmaceutical EDM package

Cyco Software , provider of engineering data management (EDM) software for process industries, has released a new package for pharmaceutical manufacturers. This module for AutoManager provides the technical controls needed for compliance with FDA 21 CFR Part 11 to manage cGMP engineering documentation throughout the enterprise. It helps bring products to market faster and boosts revenues while reducing errors in dealing with FDA and other government regulations.

“The FDA module for the pharmaceutical industry adds specific features to our core technology that enhance compliance effectiveness, reduce validation efforts, and improve document workflow throughout the enterprise,” says Bert Janssen, vice president of sales. The software enables key individuals throughout the company to access up-to-date engineering information anywhere in the enterprise at any time.

DataCore Technology, a long-standing Cyco partner, developed the FDA module to address specific data management needs among pharmaceutical customers. The module provides technical controls for compliance with FDA 21 CFR Part 11, including audit trails, electronic signatures, workflows and lifecycles, controlled printing, and security.

Cyco’s wider product line includes EDM, asset management, and application integration solutions for process manufacturers, utilities, food & drugs, oil & gas, and chemical. Cyco has almost two decades of industry experience with 275,000 users in more than 50 countries.

–Control Engineering Daily News Desk Peter Welander , process industries editor

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