Partner Spotlight | CARA Life Sciences Platform

Platform Solutions

Applications & Registrations Submission Planning & Tracking Events, Activities & Commitments Product Management including IDMP, SPOR, xEVMPD Health Authority Correspondence

submission archive

Submission Archive

submission documents

Submission Documents

promotional materials

Promotional Materials

medical device submissions

Medical Device Submissions

spor subscription

SPOR Subscription

quality management qms

Quality Events CAPAs Change Controls Deviations Management Complaints Management

quality documents management

Quality Documents Management

audit and-inspection management

Audit & Inspection Management

batch records management

Batch Records Management

learning management system

Learning Management System

quality innovations

Quality Innovations

pv case management

PV Case Management

pv system master file psmf

PV System Master File (PSMF)

safety submissions distributions

Safety Submissions and Distributions

risk management

Risk Management

medical inquiries information

Medical Inquiries

meddra integration

MedDRA Integration

safety data exchange agreements

Safety Data Exchange Agreements

ctms integrated clinical trial management

Clinical Trial Management System (CTMS)

etmf modern content management

Electronic Trial Master File (eTMF)

medical writing automatic clinical protocol generation

Medical Writing

Transform complex business processes with CARA, the unified data and content management platform for regulated industries.

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shareable

shareable

About Generis

About Us Partners Join Our Team Internship Programme

Platform Solutions

About Generis

About Us Partners Join Our Team Internship Programme

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

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.

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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