Contents
3 min read
About
The video tells the story of SteerCo, a joint initiative that aims to revolutionize the way regulated pharmaceutical information is created, managed, and shared between the pharmaceutical industry, healthcare authorities, healthcare professionals, and patients.
Video details & Credits
- Duration: 180 seconds
- Format: 2d animation
- Client: EXTEDO Pharma Software Development Bavaria, Germany
- Agency: Demodia
- Studio: Darvideo.tv
- Timing: 8 weeks
Story
When you’re not feeling well, it’s incredible how quickly modern medicine gets you back on your feet.
But, behind every medication is a long and structured process involving scientists, doctors, regulators, and life sciences professionals.
They work together to develop, test, authorize, approve, and monitor every individual medication.
Along the way, vast amounts of highly regulated information are generated and managed.
Much of this is often stored in separate, disconnected systems,
making it hard to share and use effectively.
That’s why Cormeo was founded.
Our vision is to be the trusted bridge between the industry, health authorities,
healthcare professionals, and patients.
By connecting these groups and re-engineering their way of working,
we facilitate the timely, compliant and efficient exchange and management of regulated information to improve patient health.
To follow this vision, Cormeo unites three brands, each a trusted player in their business segments.
The process starts with a plan a detailed roadmap for bringing the new medication to market.
This includes everything from running the first clinical trials to getting final approval from regional health authorities. In today’s world, pharmaceutical companies primarily manage information using traditional documents.
These documents are often static, isolated, and inefficient.
Cormeo is transforming that by introducing a revolutionary way of working: organizing content into structured components.
Unlike traditional document-based systems, Docuvera generates segments of content, making the information easier to create, update, and reuse.
This enables life sciences companies to manage their operations more efficiently and focus on innovating faster.
EXTEDOpulse serves as the central repository, seamlessly enabling the reuse of IDMP-compliant data across all Docuvera components for streamlined regulatory workflows. Once approved internally, components are transferred to EXTEDOpulse, where they are compiled into a regulatory submission.
EXTEDOpulse brings together all master data into a single, shared repository.
The final submission is validated before it’s electronically
sent to health authorities through an online gateway.
Using EXTEDOpulse for agencies, the authority assessors can quickly review
and provide feedback on individual components of the submission.
If changes are needed, the applicant can quickly identify and update the affected components.
This streamlined process saves time and ensures accuracy.
When everything is complete, and the medication is approved,
SmPC and ePIL FHIR messages are automatically transferred from Docuvera
to Rote Liste.
Rote Liste ensures that doctors pharmacists and patients receive the most up-to-date details about medicines.
Patients, too, benefit from clear, accurate information about the medicines they take.
With Docuvera, EXTEDO and Rote Liste, cormeo creates a seamless end-to-end process that makes the path from lab to patient faster, safer, and more efficient than ever before.
