Industry Provider Profiles
Company Type Services
Techorizon is an advanced technologies services provider supporting the Pharmaceutical, Medical Devices and Biotechnology Industry supplying advanced solutions and services integrating people, processes and technology.
As the Technology subsidiary of CROMSOURCE, an International CRO, Techorizon is able to draw on its parent Company’s wealth of hands-on Clinical expertise and apply it to its massive investment in technology.
Techorizon is a company born from the experience gained through Research and continuous Information Technology application conception, design and development in the Pharma and Medical Industry World, to provide, through its services, affordable and high performance solutions to its Customers.
In February 2011, the Company achieved the ISO Certification 9001:2008 considering such accreditation as the basis of the company.
Quality management and quality assurance are kept under constant review and are assiduously implemented. The quality system is revised quarterly and thoroughly reviewed once a year by an external and independent Auditor.
As a services provider of the Pharmaceutical Companies and the consciousness of the importance of data integrity and data quality in the pharmaceutical environment, led Techorizon to decide to merge the common process of the software lifecycle with the principles of the Validation according to the FDA Guidelines and GAMP 5.
The Validation principles are the following: ”Establishing documented evidence which provides a high degree of assurance that a specific process will consistently produce a product, meeting its pre-determined specifications and quality attributes”
This global quality approach is what distinguishes Techorizon from the other IT companies.
Clin-Track® is a CROMSOURCE modular solution united in a single platform which allows total management of your clinical trial in real time. It is capable of collecting and presenting 360 degrees of information from a clinical trial, from central laboratories to electronic CRFs to single patient's diaries. Through this, the sponsor has immediate access to data on all phases of their clinical trial.
- The CTMS Web application is the Clinical Trial Management System based on a long CROMSOURCE’s experience in Clinical Trials. It is a customizable web-based software application in a cloud environment, validated according to GAMP5 Guidelines and CFR Part 11 complaint.
The web philosophy reduce the cost of the application, its maintenance and the training is very short due to the likeness with the common web application.
The CTMS Web application could integrate different source of data like IVRS, EDC, etc. avoiding the manual data input.
- REPORTING MACHINE (RM) supports the generation of reports about Study Management .
The reports produced by RM can be divided in standard and custom Reports according to the Study Protocol and to the requests of the Customer.
It uses the data produced in the Data Repository via manual/automated/exchanged data input by external Data Sources like IVRS, EDC, NAVISION®, etc.
- CLOUDSHELF is a web portal to exchange files among the Study Team.
The access is restricted to authorized Users that can upload, share and download any kind of files related to the Project.
The most interesting characteristic is the possibility to manage big size files (e.g. IB, IMPD, Medical Dossier) and the users don’t need a dedicated training to use the application.
- Cloud Media Management is a tool used to manage Medical Images in Clinical Trials (e.g. MRI, Echo, X-Ray, etc.).
Investigators, Project Team, Sponsor and Medical Monitor can share the Images, review/ approve/reject them and make comments.
This application reduces the costs, allows to respect the timelines and avoids the possibility of losing the materials by couriers.
- The XePro is the revolutionary Techorizon’s solution for the collection of QoL, VAS, Patient Diary, score, symptoms, etc. in real time.
The innovative Cloud technology solves the problems related to missing information, delayed entries, inaccurate data, and faulty devices.
The XePro solutions are designed to standardize your data collection process, thus increasing the consistency of your data and ease of use for all users (Patients, Investigators, Clinical Monitors)
This technology is available for all applications as smartphone, pad, phone, laptop according to the budget and the project star-up deadlines.
Validated according to GAMP5 Guidelines and CFR Part 11 complaints.
Via Scuderlando 89/b
+39 045 8222888
+39 045 8222812 (fax)
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