Advena Ltd. provides regulatory consulting services to small and medium-sized

medical device manufacturers and distributors.

Advena Ltd. was founded in the United Kingdom in 1996 by John Adcock, Managing

Director, in response to a growing demand for high quality regulatory consulting

services by small to medium-sized emerging medical device technology companies.

Since that time, the UK office has developed a global client base involving a wide

diversity of medical devices. John has 29 years experience in medical device quality

systems.

In 2008, Advena Ltd. opened an office in the United States under the supervision of

Judy Burton, Director of US Operations, in order to provide one source for registration

of medical devices in both the European Union and United States. Thus providing

clients with the advantages of increased security and the ability to share EU technical

file information in the preparation of US FDA submissions. Judy has 9 years

experience in both the regulatory and quality systems aspects of medical devices, has

developed and implemented cGMP training programs and is certified in US

import/export regulations.

In November 2009, the UK operation expanded into new offices in Leamington Spa,

Warwickshire. These state-of-the-art offices, with conference facilities, are adjacent

the the UK motorway network and main rail links and close to Birmingham

International Airport. Heathrow is only 75 minutes away. The UK Business Manager

at Leamington is Donna Milne.

About Advena Ltd.