Medical Device Suppliers Overview
Medical Device Suppliers struggle to implement an efficient, sustainable processes to exchange accurate and ‘validated’ product data with trading partners while meeting the regulatory requirements for product identification, labeling and traceability.
The Medical Device Market
Hospitals, GPOs and regulatory agencies are all demanding reliable product data from device manufacturers to ensure patient safety, reduce operational costs, and enhance the effectiveness of post‑market surveillance. As a result, global manufacturers now face the pressure, more than ever before, to deliver on their data quality and data syndication initiatives or suffer the consequences of non-compliance.
Your Data Problems?
Trading partners and regulatory agencies each have their own data requirements. Attributes that are needed for regulatory compliance are different from those needed for procurement and supply chain management. Language requirements differ across countries while data exchange formats vary across data recipients. In this environment, device manufactures still use spreadsheets, legacy applications or point-to-point solutions that cannot scale to meet the global demand for their product data.
Our Compliance Solutions!
Innovit provides you with MDM, PIM, GDSN and UDI solutions that are purpose-built to meet your global data syndication needs. It provides you with out-of-the-box connectors for data synchronization via GDSN, as well as direct connectors to regulatory databases such as GUDID, EUDAMED and NMPA. Each connector comes pre-packaged with the relevant data attributes, code lists and validations rules along with the ability to exchange data in their respective message formats. Innovit solutions are easy to implement and will give you an affordable, yet scalable, path towards global data compliance.
Partners in Healthcare
At Innovit, our commitment to the healthcare industry is strengthened by the network of partners we have. We collaborate with fellow industry experts, thought leaders, regulatory agencies and global standards bodies to help solve your master data problems.
FDA, Med-Tech Europe, GS1 Global, GS1 Healthcare, USDM
1-click publication of product data to GDSN “out-of-the-box”.
Submit regulatory UDI data for European MDR compliance.
Submit UDI data for FDA compliance.
The ‘what’ challenge of new device regulations?
Introductory case studies about healthcare customers….
Manage and syndicate your 'trusted' master data to ALL systems and healthcare professionals!