Find IFUs and Supplier Regulatory Documentation for Tissue and Implant Products
Managing tissue and implant products often requires access to supporting documentation, including Instructions for Use (IFUs) and supplier regulatory records. During audits, recalls, investigations, supplier reviews, and day-to-day operations, teams need documentation that is easy to locate and tied to the products they manage.
UDITracker®, InVita’s tissue and implant lifecycle management platform, provides access to IFUs and supplier regulatory documents alongside tissue and implant records, giving staff one-click access throughout the product lifecycle.
For UDITracker customers, InVita helps manage IFU documentation as updated versions become available.
Request a Walkthrough
UDITracker®, InVita’s tissue and implant lifecycle management platform, provides access to IFUs and supplier regulatory documents alongside tissue and implant records, giving staff one-click access throughout the product lifecycle.
For UDITracker customers, InVita helps manage IFU documentation as updated versions become available.
Request a Walkthrough
Managing tissue and implant products often requires access to supporting documentation, including Instructions for Use (IFUs) and supplier regulatory records. During audits, recalls, investigations, supplier reviews, and day-to-day operations, teams need documentation that is easy to locate and tied to the products they manage.
UDITracker®, InVita’s tissue and implant lifecycle management platform, provides access to IFUs and supplier regulatory documents alongside tissue and implant records, giving staff one-click access throughout the product lifecycle.
For UDITracker customers, InVita helps manage IFU documentation as updated versions become available.
Request a Walkthrough
UDITracker®, InVita’s tissue and implant lifecycle management platform, provides access to IFUs and supplier regulatory documents alongside tissue and implant records, giving staff one-click access throughout the product lifecycle.
For UDITracker customers, InVita helps manage IFU documentation as updated versions become available.
Request a Walkthrough
One-click access to IFUs and supplier documentation alongside tissue and implant records in UDITracker.
When IFUs are hard to find.
Product documentation is often maintained in multiple locations. Some documents come directly from manufacturers, while others may be stored on shared drives, vendor portals, email folders, or internal document repositories.
While these approaches work, locating documentation during an audit, investigation, recall, or product review can take time. Teams may also need to verify they are reviewing the correct version of a document.
Having documentation available within the same system used to manage tissue and implant records can simplify that process and reduce the need to search multiple locations.
While these approaches work, locating documentation during an audit, investigation, recall, or product review can take time. Teams may also need to verify they are reviewing the correct version of a document.
Having documentation available within the same system used to manage tissue and implant records can simplify that process and reduce the need to search multiple locations.
Access IFUs across the lifecycle.
IFUs provide manufacturer guidance related to product handling, storage requirements, preparation, use, and other product-specific instructions. While they are not needed during every workflow, organizations may need access to them when questions arise about a product or process.
Documentation may also be reviewed during audits, recalls, investigations, staff training, competency reviews, or other compliance activities.
UDITracker makes documentation available alongside related tissue and implant records, helping users access supporting information while reviewing inventory, products, and case activity.
Documentation may also be reviewed during audits, recalls, investigations, staff training, competency reviews, or other compliance activities.
UDITracker makes documentation available alongside related tissue and implant records, helping users access supporting information while reviewing inventory, products, and case activity.
One platform for tissue and implant documentation.
UDITracker stores IFUs and supplier regulatory documentation alongside tissue and implant records.
Documentation remains connected to the products and records being reviewed, helping teams locate information more efficiently when questions arise.
For organizations managing tissue and implant products, this helps keep documentation and related records easier to access from one place.
Documentation remains connected to the products and records being reviewed, helping teams locate information more efficiently when questions arise.
For organizations managing tissue and implant products, this helps keep documentation and related records easier to access from one place.
Supplier documentation, centralized.
In addition to IFUs, organizations are often responsible for maintaining supplier regulatory documentation.
UDITracker provides a centralized location for supplier records, which may include FDA tissue establishment registrations, state licenses, accreditation records, and other supplier credentials.
Keeping these records organized and readily available can help simplify supplier reviews, audit preparation, and documentation requests.
UDITracker provides a centralized location for supplier records, which may include FDA tissue establishment registrations, state licenses, accreditation records, and other supplier credentials.
Keeping these records organized and readily available can help simplify supplier reviews, audit preparation, and documentation requests.
Ready for audits, recalls, and reviews.
Documentation needs do not stop when products are used.
Organizations are often asked to provide supporting documentation during audits, recalls, investigations, supplier reviews, and other compliance activities. Having documentation readily available can help reduce the time spent searching for records across multiple systems or locations.
UDITracker maintains IFUs and supplier regulatory documentation associated with products, inventory, and cases, helping teams access supporting records when needed for audits, recalls, investigations, and routine reviews.
This provides a centralized location for documentation and related product activity, helping organizations respond to requests more efficiently.
Organizations are often asked to provide supporting documentation during audits, recalls, investigations, supplier reviews, and other compliance activities. Having documentation readily available can help reduce the time spent searching for records across multiple systems or locations.
UDITracker maintains IFUs and supplier regulatory documentation associated with products, inventory, and cases, helping teams access supporting records when needed for audits, recalls, investigations, and routine reviews.
This provides a centralized location for documentation and related product activity, helping organizations respond to requests more efficiently.
Support for Joint Commission tracer reviews.
During Joint Commission tracer activities, organizations may be asked to demonstrate product history, documentation, and chain of custody information associated with a patient encounter.
UDITracker’s Patient Tracer helps connect tissue and implant records with related case activity, inventory history, and supporting documentation.
When documentation requests arise, teams can review information from a centralized location rather than relying on multiple systems or institutional knowledge to locate records.
UDITracker’s Patient Tracer helps connect tissue and implant records with related case activity, inventory history, and supporting documentation.
When documentation requests arise, teams can review information from a centralized location rather than relying on multiple systems or institutional knowledge to locate records.
IFU and regulatory documentation, simplified.
Access to product and supplier documentation is an important part of tissue and implant management.
By maintaining IFUs and supplier regulatory documentation within UDITracker, organizations can keep documentation connected to the products and activities they support.
Whether preparing for an audit, responding to a documentation request, reviewing a case, or managing day-to-day operations, teams have access to documentation within the same platform used to manage tissue and implant workflows.
By maintaining IFUs and supplier regulatory documentation within UDITracker, organizations can keep documentation connected to the products and activities they support.
Whether preparing for an audit, responding to a documentation request, reviewing a case, or managing day-to-day operations, teams have access to documentation within the same platform used to manage tissue and implant workflows.