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Applications & Registrations Submission Planning & Tracking Events, Activities & Commitments Product Management including IDMP, SPOR, xEVMPD Health Authority Correspondence
submission archiveSubmission Archive
submission documentsSubmission Documents
promotional materialsPromotional Materials
medical device submissionsMedical Device Submissions
labellingLabelling
spor subscriptionSPOR Subscription
quality management qms
Quality Events CAPAs Change Controls Deviations Management Complaints Management
quality documents managementQuality Documents Management
audit and-inspection managementAudit & Inspection Management
batch records managementBatch Records Management
learning management systemLearning Management System
quality innovationsQuality Innovations
pv case managementPV Case Management
pv system master file psmfPV System Master File (PSMF)
safety submissions distributionsSafety Submissions and Distributions
risk managementRisk Management
medical inquiries informationMedical Inquiries
meddra integrationMedDRA Integration
safety data exchange agreementsSafety Data Exchange Agreements
ctms integrated clinical trial managementClinical Trial Management System (CTMS)
etmf modern content managementElectronic Trial Master File (eTMF)
eTMF ArchiveeTMF Archive
medical writing automatic clinical protocol generationMedical Writing
Transform complex business processes with CARA, the unified data and content management platform for regulated industries.
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shareable
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About Generis
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Platform Solutions
About Generis
About Us Partners Join Our Team Internship Programme
Events
Resource Hub
Contact
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)
eTMF ArchiveeTMF Archive
Medical Writing
Transform complex business processes with CARA, the unified data and content management platform for regulated industries.
cara elastic
shareable
shareable
shareable
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Our Mission

Generis is a leader in content and information management systems, specializing in proven solutions for regulated industries. Our mission is to provide industry-defining implementations that are fast and intuitive in order to bring our customers an enjoyable and efficient experience that allows them to focus on their work. Generis offers unprecedented care and attention by listening and responding to our customers, and innovatively driving the future of information management.

ISO27001 is an international standard on how to manage information security – a core requirement for companies providing SaaS solutions in regulated industries.

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