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About Us

A full service regulatory consultancy, we employ only experienced professionals. We are helping pharmaceutical and biopharmaceutical companies with regulatory affairs advice, submissions and compliance and have clients based in Europe, America and Asian countries.

Many clients tell us that what they really appreciate is the continuity of the service that we offer. Where possible, we make sure that your designated project team leader stays with you throughout the lifetime of your project. We will work with you on a one-to-one basis to monitor progress and to ensure that agreed milestones and deadlines are met and that your project reaches a timely and successful conclusion.

Our regulatory team have the skills and proven ability to advise on and manage a variety of regulatory projects of all sizes.

We have a rich multicultural background which many clients find invaluable. Our collaboration with a network of overseas associates strengthens our capability to run international projects. Our presence covers all EU countries plus several other European ones (Austria, Belgium, Bulgaria, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovenia, Spain, Sweden, Slovak Republic, Switzerland, Russia, Ukraine) as well as the USA and Japan - just what is needed in the international environment of your regulatory projects.

We know that even the best resourced regulatory affairs departments need additional support at peak times and the team at Cambridge Regulatory Services has gained a reputation for delivering projects on time and within budget for its clients across the world.

Relentlessly striving to exceed their clients' expectations, Cambridge Regulatory Services enables you to remain focused on your key objectives while our team of professionals takes care of your short-term or long-term regulatory needs.