In the highly competitive Medical Device market, time-to-market, compliance, and continual improvement are instrumental.
From design to post market, managing change to the device is critical. A seemingly small process deviation or change to a component can cause major problems such as product quality issues, patient safety, data loss, and possible regulatory actions or recalls. Our Medical Device division helps our customers bring their products to market faster, monitor their products in the field, and handle post-market surveillance while addressing a variety of regulatory challenges unique to the Medical Device industry.
How We Help Medical Device Manufacturers
USDM offers comprehensive services to help navigate a complex regulatory landscape, including compliance and quality strategy and execution, audits and assessments, remediation, validation and qualification, global product identification and much more.
Whether you are a large global medical device manufacturer or a small startup new to the regulatory landscape, USDM can help to define a top-to-bottom risk management strategy to ensure resources are aligned, profitability is maximized, and regulatory exposure is minimized.
USDM can help build an IT roadmap that lays out your strategy and governs how technology will support your business growth over the next 3-5 years. With 20 years of compliance and IT expertise, we have lived through many technological advances and helped accelerate many life science organizations to deploy data, applications, technology, and capabilities that drive innovation.
Life science organizations want to use cloud technologies in regulated areas – getting rid of costly on-premises solutions that no longer meet their business needs – but compliance has always been a concern. USDM can help with selecting the right cloud vendor to meet your business needs and achieve and maintain continuous GxP cloud compliance without the headache.
USDM offers extensive services to ensure medical device companies are accurately submitting their UDI data to the European Databank on Medical Devices (EUDAMED) and other regulatory agencies including; complete assessment of supply chain and regulatory activities, inventory of medical devices, process improvements, overall readiness, and a fast-start US UDI Class 1 Medical Device Compliance Toolkit to prepare for the FDA's September 24, 2022 deadline.
USDM offers both managed services and project-based solutions to help plan, execute, and manage any or all enterprise-wide activities necessary to meet European Medical Devices Regulation (MDR) and In-vitro Diagnostics Regulation (IVDR) requirements.
USDM’s Digital Transformation solutions help life sciences customers get products to market faster, decrease IT spend and footprint, and enable compliant digital transformation. Our in-depth technical know-how and vast industry experience provide best-practice digital transformation strategy and implementation with a focus on compliance. Our technology roadmaps and fast-start solutions accelerate regulated companies of all sizes.
for medical device manufacturing solutions.
Relevant content for medical device manufacturers
Webinar: Evolving Global UDI Product Data Requirements
Blog: More Medical Device Implications of Brexit
Blog: Key differences in the requirements for SFDA UDI and US & EU UDI
Webinar: How to Comply with Saudi Arabia UDI Requirements
Podcast: EP 3: Global UDI and EU MDR Requirements