In order to pass an upcoming FDA inspection, our client needed specialized support. Discover how Oxford's partnership made the difference. 

Discover how Oxford’s team of medical writers completed 150 scientific validity reports within five months.

Discover how Oxford helped a pharmaceutical manufacturer open a fully validated facility within eleven months. 

A medical device manufacturer was in need of installing and qualifying a completely new piece of automated manufacturing equipment. Learn how Oxford's experts helped our client create a compliant system. 

Discover how Oxford’s talent helped meet the deadline and complete the facility expansion.

Discover how Oxford promptly provided 15 consultants that were critical to achieving an observation-free site inspection.

Discover how Oxford’s consultants helped to remediate the issue and pass the FDA re-inspection.

Discover how Oxford provided assistance to keep the project on track.

Discover how Oxford consultants revised a Quality Management System to meet FDA regulations within seven weeks.

Discover how Oxford’s team helped create an FDA-compliant automated production process.

Discover how Oxford’s team quickly helped capture and address issues to achieve full compliance. 

Discover how Oxford’s team of experts completed product-specific and State-of-the-Art Literature Searches within four months.