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MaxisIT FSP Electronic Clinical Documents Management System (eCDMS) integrates the capture, conversion and distribution of paper and electronic information – allowing for a simple, efficient and controlled electronic distribution into a variety of information systems simultaneously. It is easy to implement, cost-effective and can be implemented even in most complex and heterogeneous environments. Version control, audit trails, and work-flow mechanisms are other value added features to the over all solution.
MaxisIT eCDMS is scalable, intuitive and is easy to use allowing for a faster, more efficient workflow. It can capture different type of patient information from a number of different devices. This, coupled with the availability to track, sort, archive, and re-use document routing rules, eliminates the need for redundant work and significantly enhances productivity of your staff. It is capable of distribution of clinical information or documents into multiple destinations such as fax, e-mail, document / clinical information systems / records management systems etc., simultaneously and allows for enterprise-wide deployment quickly and cost-effectively – Truly business without boundaries. Document tracking, versioning and security are critical; knowing who is handling what, which is the latest version and what has been modified, when was the change made is a business imperative. MaxisIT eCDMS empowers end users with embedded document directives and ensures that each and every document is audited and retained, resulting in improved accountability and compliace with 21 CFR Part 11. We can help you manage sensitive patient matter, control distribution and delivery, reduce unnecessary paper documents (via electronic storage) and provide enterprise-wide connectivity resulting in cost savings MaxisIT Electronic Clinical Documents Management System provides full access, flexibility and digital security as Pharmaceutical and Life Sciences customers struggle to cope with the challenges of regulations, disaster recovery and paper-intensive workflows. MaxisIT Services Include: -
Trial documents design and planning process -
Efficient document collection and management of total patient and trial data documents -
Maintaining FDA compliance documents -
Centralized, secure access to sites, trials -
Data entry accuracy in documents -
Complete documents validation -
Total electronic documents audit trail
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| Clients |
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Client Online is a password-protected site that provides Project knowledge base, project management tools, and the other documents. If you are a MaxisIT client with a current contract and would like access to our portal, please send an email from your company domain address to |
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| Success Stories |
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A major pharmaceutical organization accomplishes FDA eSubmissions with the help of MaxisIT. MaxisIT standardizes clinical trial systems for a large pharmaceutical organization with the help of CDISC data standard models.
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| Testimonials |
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I recommended that our IT and Operations groups partner with MaxisITInc because they are an independent company that can function as an advisor to our organization. Their experiences and capabilities allow them to act as a translator and trainer between Information Technology and our business units.
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| Services Contact |
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Contact our Services Specialist at our Corporate Headquarters in Metuchen, NJ. MaxisIT Inc. 203 Main Street, Metuchen, NJ-08840 Ph.732-494-2005
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| CT Renaissance |
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| Clinical FSP |
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