Organize All Documents
Create a centralized database with approval workflow and audit trails.
Meet FDA, ISO, EPA and OSHA standards and regulations with adaptable workflows that support your unique processes. Gain valuable insight into your quality data, make smarter decisions faster, and leverage AI to save become more efficient.
Create a centralized database with approval workflow and audit trails.
Meet any FDA, ISO, EPA, OSHA or any GxP Compliance requirements worldwide.
Reduce document cycle time by speeding up routing, delievery, revision, and approval of documents.
Worry less about product recalls by creating workflows to identify problems & document preventive procedures.
Improve user adoption by modifying your compliance software to match your business processes.
Receive reminder emails according to the established audit schedule.
• Eliminate redundancy, reduce the risk of manufacturing products, create efficiency in organizing documents from suppliers and others.
• Become more lean and efficient as your organization understands what training and skills are in-house and what new competencies are required.
• Customizable reports that deliver relevant data to your users.
“I love how the program is fully customizable. Easy to manage and configure on my own. We have seen very positive feedback during audits at how we use Intellect to improve our company.”
"Intellect is an extremely capable and flexible solution that does not require an organization’s skilled IT resources to configure, manage, or solution."
“Intellect allowed us to streamline the implementation, review, and revision of our standard operating procedures. It also helped with making the process shorter and digitalizing everything instead of working on hard copies.”