Regulatory Compliant Document Management for Pharmaceutical and Healthcare Industries.
Companies in the Pharmaceutical, Biotechnology, and Medical Device Industries cannot afford to risk their reputations or their licenses to operate. They must ensure compliance at all times. They face stringent government compliance requirements, which require Comprehensive Auditable Control of all asset information.
Do you need to meet strict regulatory compliance requirements for electronic records and documents?
Are you worried about staying compliant with FDA 21 CFR Part 11?
Consider Accruent’s engineering document management solution, Meridian. Comprehensive and powerful, Meridian can help your company comply with FDA 21 CFR Part 11 while also providing a strong backbone of data management and maintaining your engineering data integrity.
Pharmaceutical companies like Abbvie, Pfizer, Johnson & Johnson and Sanofi trust Meridian to help their organisations reduce average search times for relevant documentation from hours to minutes, and ensure regulatory compliance.
The Benefits of a Compliant
Robust Electronic Signature Management
Watermarks/Print Stamps to Increase Visibility
Managed Change (with Approval Workflows and Notifications)
Audit Trails (Showing what has Changed by Who and When)
Let us show you a world-class system — our Meridian platform.
We invite you to learn more from our webinar and demonstration.
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The right healthcare regulatory compliance software can help organizations in the healthcare industry maintain compliance, mitigate risk, improve their finances and more – even amidst constantly changing requirements and protocols. Here’s everything you need to know about regulatory compliance, compliance software, and key features to look out for.Learn More
Find out more about Meridian Cloud for Life Sciences.
Transition to the cloud, simplify compliance and streamline validation with Accruent’s highly secure, expertly validated SaaS EDMS.Watch Demo
Register for our Webinar recording to discover how Meridian can help your organisationRegister for Webinar
Capabilities of Meridian Cloud for Life Sciences.
The Life Science industries are changing, and key players are moving to the cloud. Why? The world is more remote than ever, and ever-changing regulations and multi-site operations are calling for more system automation, improved validation and increased focus on mobile regulations.
That’s why Accruent has released Meridian Cloud for Life Sciences.
Meridian Cloud for Life Sciences is an expertly validated, cloud-based engineering document management system (EDMS) that simplifies compliance, streamlines validation and helps modern Life Science organizations transition to the cloud.
Join this webinar to learn more about key capabilities of Meridian Cloud for Life Sciences and how the software can support your maintenance, reliability and operations teams.
Watch the Demo
Lead your industry with Meridian Cloud for Life Sciences.
Transition to the cloud, simplify compliance and streamline validation with Accruent’s highly secure, expertly validated SaaS EDMS.
Pharmaceutical Industry Trends
Learn more about Healthcare Regulatory Compliance Software!
The right healthcare regulatory compliance software can help organisations in the healthcare industry maintain compliance, mitigate risk, improve their finances and more – even amidst constantly changing requirements and protocols. Here’s everything you need to know about regulatory compliance, compliance software and key features to look out for.
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