Maximize Performance of Your Mission-Critical Assets While Safeguarding Compliance

Pharmaceutical / Life Sciences

Companies in the life sciences industries, like pharmaceutical, biotechnology, medical device, and others, can’t afford to risk their reputations or their licenses to operate. They must ensure compliance at all times as they face stringent government requirements, including more system and workflow automation, improved software validation, mobile regulation, and auditable control of all asset information and technical documents.


Pharmaceutical / Life Sciences Process Manufacturing Industry-Related Products

Engineering Document Management System (EDMS) Software for Pharmaceutical / Life Sciences

An expertly validated, cloud-based engineering document management system (DMS) that helps your life science organization transition to the Cloud while driving operational efficiency. You can track all asset information, control digital documents’ revision history, access, and accuracy, streamline validation and regulatory compliance, speed product time to market, and protect quality management.

Meridian Cloud for the Life Sciences Industry

Bringing the right products to market at the right time is essential to innovation for life science companies. And it’s critical to maximize market success and lower product liabilities by reducing risks through compliance and software validation.

Read the whitepaper to see how life sciences organizations address these challenges, including accelerating digital transformation and leveraging engineering document management software with added validation services, such as Meridian Cloud for Life Sciences.

Speed Up Time to Market by Improving Engineering Data Integrity

Manage vast amounts of engineering information and always access the most current and approved engineering documentation while providing a complete audit trail to regulatory bodies.

Meridian is an engineering document storage and management solution that can help your life sciences organization maintain FDA 21 CRF Part 11 compliance and validation efforts for all electronic documents while at the same time ensuring greater efficiency and good manufacturing practices (GMP).

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