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Standards

DO NOT LOSE THE THREAD AND PULL THE RIGHT STRINGS

The amount of raw-data has increased year by year in drug research and development. New technologies and simply the available storage have created mountains of unstructured data that cannot be assembled by a simple human interaction.
At the same time, regulatory requirements are forcing companies to keep track of the created data, ensure data integrity and to control the retention.
The value lies in the data, so you should be able to find your data, be able to access, to inter-operate and to finally re-use data at any time in your product life cycle.

Collecting data at the point of creation, enrichment with context and annotations, even supported by machine learning and artificial intelligence all in fully controlled process flows, subsequent quality-checks, evaluation, validation and later archiving.

Untangle your Data and follow the data in your decentralized universe.
Pull the right strings! Be ready for any inspection! Access data easily!

platform

WHAT IF A PLATFORM CAN BRIDGE THE ENTIRE PROCESS END-TO-END?

Sustainable success in the modern era lies beyond standalone streamlined processes. Everything is now interlinked. More than ever, all technical processes rely on imaging. Images are the heaviest data storage and computational burdens of the modern technology organization and hoard vast untapped information (at unmeasured costs).

neuronOS is based on a keen awareness of the drivers in pharmaceutical development; prudently disrupting or blending in. It is built specifically to support Advanced Analytics on Big Data and enable Artificial Intelligence on multiple levels to increase speed and enable the right data-driven decisions. Instead of being slammed by frequent regulatory waves, organizations neuronOS to ride on top of them.

Enabling a smart digitization from early stages onwards by utilizing metadata in all asset types, in big data volumes from screenings, 2D/3D imaging and annotation processes
Understanding success factors in Clinical Trials and Regulatory Submissions increase the probabilities and enable early attrition by predictive analysis.

Turning massive data into valuable information which can lead into earlier decision readiness. Making the right decisions early is paramount. Understanding fundamental functional patterns manifest in digital forms and workflows which are core principles of the biomedion approach - all with quick and data-driven decisions in mind.

the main principles

ALCOA / ALCOA+

FINDABLE

Be able to find your data! By using rich metadata and keywords you can run your system appropriately with a searchable resource.

ACCESSIBLE

Be able to find your data! By using rich metadata and keywords you can run your system appropriately with a searchable resource.

INTEROPERABLE

Use a formal, accessible, shares and broadly applicable language for knowledge representation.

REUSABLE

Reusability is the one of the most critical things. Use a plurality of acccurate and relevant attributes and make the data available to use!

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Intelligent raw data archiving watcher

Processes, Documents, RAW Data, GxP Lab, Controls, SEND, IoT

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intelligent pharma quality management

QMS, qDMS, CAPA, Image QC, Issue Management​


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Intelligent trial master file

Processes, Documents, DIA eTMF, CRO Migration, Longterm Archiving

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intelligent regulated content services

Regulatory Document Management (rDMS), promo mats​


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