Discover how the right Oxford consultants were able to provide support for a Data Integrity Remediation project when a client needed niche expertise. INDUSTRY Pharmaceutical SERVICES Remediation SKILLS ISO Compliance The Challenge A global pharmaceutical manufacturer...
Discover how Oxford’s expert consultants enabled a smooth production process by reviewing six months of inaccurate data. INDUSTRY Pharmaceutical SERVICES Quality Assurance Remediation SKILLS Empower V2 The Challenge A research-based biopharmaceutical company was in...
Discover how Oxford helped our client qualify 50 combination products in 3 years. INDUSTRY Pharmaceutical Medical Device Manufacturer SERVICES Commissioning & Qualification Product Development Remediation SKILLS ISO Compliance Project Management Test Method...
Discover how Oxford helped a medical device manufacturer start their MDR compliance journey the right way. INDUSTRY Surgical Instruments SERVICES European Medical Device Regulations (MDR) SKILLS Risk Mitigation & Management Quality Assurance The Challenge A...
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. INDUSTRY Medical Manufacturing SERVICES Facilities and...
Meet Alison: Alison began working for Oxford about a year ago, when she was introduced to her Oxford recruiter Josh by a former colleague. She was originally working with another consulting firm, but once her placement ended, that firm would not actively look for...
It’s our 35th anniversary, and we couldn’t be more excited. To celebrate this milestone, we wanted to take a moment to recognize how much we truly love what we do. So, we came up with a list of 35 reasons why we love working in the staffing and recruiting industry....
As the May 26, 2022 deadline has come and gone, now it is more critical than ever to evaluate what your organization needs to accomplish. If this feels like a daunting task, you’re not alone, as many organizations are facing the same challenges. The differences...
In May 2017, EU officials announced regulations impacting organizations that manufacture in vitro diagnostic devices in both Europe and the United States. In order to sell their products on the European market, organizations must achieve compliance with these new...
