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The Clinical Data Management (CDM) Group at MaxisIT has expertise in the area of cumulative data management. This group evaluates the trials in the design phase in order to create an efficient data management process specific to the studies needs – a process that enables us deliver a clean, locked database with a minimal amount of errors; delivered on time and within budget, always. 
MaxisIT FSP offers the following CDM services to its customers - - Protocol design & review
- Randomization schedules
- Case report form (CRF) design & review
- Database design
- Data entry
- Data validation/verification
- Data transfer
- Medical term coding
- Quality management procedures
- Data manipulation
- Electronic data capture
- Setup of data management policies and procedures.
- Development of global library objects.
- Setup of studies in EDC and clinical databases.
- Building and implementing edit checks and data cleansing utilities.
- Development of validation and derivation procedures.
- Resolution of DCFs.
- Maintenance of dictionaries.
- Coding of adverse events and concomitant medications.
- Achieve timely database lock.
- Migration of clinical data from legacy systems to newer CDMS.
Our goal is to help reduce the cycle time from the first patient in to the database lock and we help customers achieve that. MaxisIT FSP CDM group with over 30 data management experts, several of them with multi-vendor EDC experience, have assisted our clients in the past with the following specialized services - Review & Plan: Our experts start by understanding the clients needs, review and validate the current architecture, make a project plan, implement / support / execute the plan and train the employees. Training: We train the clients employees in-house / onsite through easy to understand practical coursework and materials. Validation: Manage the validation process, write or modify SOPs and perform audits. Help with Implementation / Support: We have the expertise in developing SOPs, building global libraries, initiate and execute pilot projects (including set up and management), write procedures and identify integration points.
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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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