Siloed systems for training, quality, and documentation management create compliance gaps
Manual updates cause outdated SOPs to remain in circulation without progress
Lack of integration makes tracking the status of regulatory compliance training inefficient
No unified view of audit readiness or employee qualifications
Compliance teams spend more time maintaining tools than improving compliance
Most alternatives don’t unify LMS, QMS, and DMS
Limited audit support creates last-minute stress
Rigid workflows fail to meet pharma compliance needs
Deployments drag on for months instead of weeks
Limited support leaves teams without needed guidance
Assign training automatically when SOPs or regulations change
Manage regulatory compliance training, quality incidents, and documents in one system
Ensure every compliance document is automatically updated, approved, and traceable with secure electronic signatures
Track completions, overdue tasks, and audit readiness instantly.
Tailored configurations to match your pharma processes—without added cost
100% training completion rates with automation
100% audit-readiness achieved in minutes
50-75% reduction in administrative tasks thanks to automation
Prepare or produce audits within minutes instead of weeks
Reduced Risks, avoid potential regulatory fines and lawsuits
“SyberWorks is user-friendly, easily customizable to meet different user requirements. It helped the company to comply with regulations and provided a structured framework to identify and understand the regulatory requirements.”
“SyberWorks has transformed how we manage our studies. The platform saves time, reduces errors, and, most importantly, their customer support is outstanding, always ready to help and tailor solutions to our needs.”
“We couldn’t be more pleased. I mean, as you’ve seen, we’re adding more and more things to the system because we can make it work for us, and it’s really wonderful! It’s really helped us.”
Learn any time, any place. Highly tailored to your organization’s needs.
