Discover how the right Oxford consultants were able to provide support for a Data Integrity Remediation project when a client needed niche expertise.
Oxford Global Resources Expands Capabilities in Workday® with Acquisition of Hale International
Oxford Global Resources is pleased to announce that it has acquired Hale International, a leading provider of Workday® staffing and consulting services in the US.
Case Study
Case Study
Discover how Oxford’s expert consultants enabled a smooth production process by reviewing six months of inaccurate data.
Case Study
Discover how Oxford helped our client qualify 50 combination products in 3 years.
Case Study
Discover how Oxford helped a medical device manufacturer start their MDR compliance journey the right way.
Case Study
Due to a facility expansion, a global pharmaceutical manufacturer needed to engage with an organization that could provide Commissioning, Qualification and Validation services. Learn how Oxford delivered.
News & Events
Visit Oxford Global Resources to learn why having the right partner for your project is essential. We connect you to the highest caliber of talent for your staffing and consulting needs. Let us deliver The Right Talent. Right Now.®
Article
Alison is an Epic™-certified Laboratory Information Systems Consultant with a passion for installing and supporting products. The ever-changing nature of her role makes her excited to work with her clients and find innovative solutions.
Article
The 2019 MedTech Summit in Brussels was an event chock full of information and insight. This year, with more than 250 meetings over the course of five days, the main focus was a deep dive on the many facets of MDR and IVDR. Over 500 MedTech managers, directors, and executives were in attendance, all with the goal to learn as much as possible about these regulations and the various factors involved in achieving compliance before the upcoming deadlines.
News & Events
Oxford is proud to be a sponsor of the 2019 MedTech Summit. Oxford consultants are MDR/IVDR experts and can help you achieve compliance within upcoming deadlines. Connect with us at the summit on the 18th and 19th of June to discuss your project needs.
Article
Although the May 2022 deadline for the upcoming In Vitro Diagnostic Regulations (IVDR) might seem distant, now is the time to evaluate what your organization needs to accomplish before these key dates arrive.
Article
In May 2017, EU officials announced regulations impacting organizations that manufacture in vitro diagnostic devices in both Europe and the US. In order to sell their products on the European market, organizations must achieve compliance by May 2022.
Article
Each year, the FDLI conference in Washington, DC is a valuable opportunity to interface with industry leaders and participate in a multitude of educational sessions. With this year’s conference rapidly approaching, we look forward to the learning opportunities we will undoubtedly experience.