Life Sciences 2021-07-20T16:21:45+10:00

 

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 organizations reduce average search times for relevant documentation from hours to minutes, and ensure regulatory compliance.

The benefits of a compliant platform

  • 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 case study.

We have the resources to help:

Webinar

Register for our Webinar recording to discover how Meridian can help your organisation

Register with the link below.

Case Study

A case study from an organisation that has met similar challenges.

How AbbVie maximized efficiency with compliant control of engineering information management.

Learn More

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.

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.

.

Register for the Webinar recording

Case Study

How AbbVie maximized efficiency with compliant control of engineering information management

The ongoing global rollout and centralization of Meridian allows AbbVie to share documents and align business processes across manufacturing sites worldwide. AbbVie now maintains vital compliance with FDA 21 CFR Part 11 throughout the drawing and asset lifecycle, and the IBM Maximo integration provides smooth access to critical asset data for Maintenance.

View Case Study

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.

Begin a conversation

Maintain Compliance and Mitigate Risk

We look forward to working with you!

    %d bloggers like this: