The comprehensive platform
for Life Sciences.

CARA is the world’s first enterprise workspace designed specifically for regulated industries, offering a simple, unified way of working with business-critical content and information.

The platform delivers secure, versatile, and scalable solutions both in the cloud or on premise, alleviating the need for investment in multiple siloed solutions.

Regulatory

Regulatory

Simplify your regulatory processes on one intuitive and scalable platform

Streamline your business processes

  • Submission documents (Pharma, Devices, Consumer, Veterinary)
  • Labelling
  • Sales & Marketing
Quality

Quality

Centralising Quality Management

  • Quality documents
  • QMS (Deviations, Complaints & Audits)
  • QMS (Quality Events, CAPAs & Change Requests)
  • Learning Management (LMS)
Safety

Safety

Manage and gain real-time insight of adverse events

  • Pharmacovigilance Case Management
  • Adverse Event Management
  • Medical Inquiries
  • PSURs & Educational Materials
  • Safety Data Exchange Agreements
  • PSMF
Clinical

Clinical

Innovative and flexible solutions for better visibility

  • eTMF
  • Clinical study management (CTMS)
Enterprise

Enterprise

Powerful Enterprise Productivity

With CARA you can manage enterprise traceability, security and collaboration on one regulated workspace.

  • Content Management
  • Data Management
  • Case Management
  • Internal & External Collaboration
  • Financial Documents
  • Legal / Contracts
  • Structured Content Authoring
  • Human Resources

“Senior leaders from across the AstraZeneca business were genuinely taken by surprise by the extent of the positive reaction to CARA … they had never before seen such a turnaround in user sentiment from a system improvement initiative, nor one accomplished so seamlessly and smoothly.”

ASHLEY BIRCH Global Head, Information Strategy Systems and Analytics, AstraZeneca

CARA in numbers

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60% of the top global 15 Life Science companies use CARA
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Used by over 500,000 industry experts worldwide!
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Contributed in the development of all the current XX drugs on the market.
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Supported Clinical trials in XX countries.
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Help developed XX rare and Orphaned drugs.
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Annual encounters XXX patients.

Find out all our latest News here!

Unlock Your Vaults

Learn how CARA can help replace the pains of siloed ’vaults’, and create a seamless content and information flow in your Enterprise.

Take the challenge at no cost and see how CARA can replace your individual solutions with a truly integrated platform.