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Transform complex business processes with CARA, the unified data and content management platform for regulated industries.
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About Generis
About Us
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Join Our Team
Internship Programme
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Applications & Registrations
Submission Planning & Tracking
Events, Activities & Commitments
Product Management including IDMP, SPOR, xEVMPD
Health Authority Correspondence
Submission Archive
Submission Documents
Promotional Materials
Medical Device Submissions
Labelling
SPOR Subscriptio
Quality Events
CAPAs
Change Controls
Deviations Management
Complaints Management
Quality Documents Management
Audit & Inspection Management
Batch Records Management
Learning Management System
Quality Innovations
PV Case Management
PV System Master File (PSMF)
Safety Submissions and Distributions
Risk Management
Medical Inquiries
MedDRA Integration
Safety Data Exchange Agreements
Clinical Trial Management System (CTMS)
Electronic Trial Master File (eTMF)
Medical Writing
Transform complex business processes with CARA, the unified data and content management platform for regulated industries.
Learn more about the CARA foundational platform
Download
Download
Download
Schedule a demo
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About Generis
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CDCR Upgrades Document and Records Management Processes with Generis’ CARA Platform
