[span6]The InnovoPOINT® portal is a core product module in InnovoCommerce’s eClinical Collaboration Suite. It helps global clinical sponsors to better organize, manage and streamline the life-cycle of studies from site feasibility through study start up, conduct and close out. The solution’s configurable features, secure document workflow engine and clinically-focused functionality facilitate compliance with FDA 21 CFR Part 11 regulations. By deploying innovoPOINT®, clinical sponsors ensure that investigator relationship management and secure clinical document exchange are managed efficiently and effectively.
Download the innovoPOINT® solution brochure: [button text=”Download” link=”http://www.innovocommerce.com//wp-content/uploads/2014/03/InnovoPOINT_Clinical_NEW.pdf” style=”default” size=”normal” target=”_blank” display=”inline” icon=”book”]
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- Enhance Relationships: Single-sign on (SSO) allows investigative site users to access their study using one username and password. Improve and streamline communication with investigative sites to build and maintain solid business partnerships for successful long-term collaboration on clinical studies.
- Accelerate Site Activation: Streamline key processes for site activation by accelerating site training and enabling essentialsecure document exchange with investigator sites to shorten study start up completion times.
- eTMF/eISF Oversight and management of essential document workflow: Enable real-time management and quality control over your clinical collaborative processes and document exchange. Reduce time to submission by closing out your trial with a complete and accurate trial package.
- Integration With eClinical Systems: Standard integrations with CTMS, SAE, EDMS and other key eClinical systems ensure the short and long-term adoption of the portal with the study teams across all time zones and cultures.
- Part 11 Compliant Training: Enables the creation, management, tracking and publishing of complaint training modules and certificates. Training expiration and renewal dates are automatically tracked in the system.
- Intelligent Document Distribution: Ensures that information reaches the right site personnel at the appropriate time and within the compliance framework.
- Automated clinical trial provisioning with out-of-the-box portal site templates, sub-site templates, document libraries, metadata, lists and workflows
- Self-service management of passwords and user account requests
- New user creation with guided workflows
- Highly scalable external user identity database management
- Ability to invite potential investigators to the portal to enter their basic information and site details
- Administrative super user system monitoring, usage and audit trail reporting
- Bulk import utility for integration with underlying clinical trial management (CTMS) and investigator data base systems
As a fully hosted solution, innovoPOINT® does not require investment in hardware or infrastructure to get up and running. innovoPOINT® can be implemented faster than any other enterprise clinical and investigator portal given the fully configurable, scalable nature of our product. Our integrated team of technologists, business analysts and clinical experts work with your team to translate business requirements into the innovoPOINT® portal solution – for enterprise, program, and study level clinical initiatives. Our flexible delivery model allows clients to drive the implementation or leverage InnovoCommerce’s professional services to supplement their internal team and infuse industry best
practices when introducing the portal to their investigators around the globe.
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- Turnkey service to provision and manage on-demand qualified Study Management environments
- Turn prohibitive eClinical CAPEX outlays into OPEX
- Infrastructure qualification and product validation services
- Ongoing support and management of study management application in compliance with FDA/GxP requirements
- SAS 70II data center with complete set of capabilities and services
- US-EU Global Safe Harbor certified facility
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