Lack of integration between training, quality, and documentation systems
Inability to support FDA 21 CFR Part 11 requirements like e-signatures and audit trails
Limited flexibility to align workflows with SOP and CAPA procedures
Manual data handling increases errors and non-compliance risk
High customization costs make compliance automation inaccessible to smaller teams
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
Auto-assign training when SOPs or regulations are updated
Eliminate silos with one platform for training, documentation, and CAPA management
Generate audit reports in minutes with electronic signatures and full traceability
Tailored to fit your pharma operations without any extra cost
Assign and track compliance training by job role, department, or competency
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.
