Medicom Consulting

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Welcome to Medicom Consulting PDF Print E-mail

Medicom Consulting provides professional support in quality and regulatory affairs management to the Medical Device, Diagnostic, Biological, and Pharmaceutical Industry. Our support services are designed to help companies to improve compliance levels with US, EU and other national regulations, thereby improving product quality, safety and effectiveness, and avoiding difficult financial and reputational problems associated with adverse regulatory inspections.

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Our goal is to assist you attain operational excellence.

Since Medicom Consulting was established in 1995, by Tom Donnelly and Ron Pagan the partnership along with carefully selected associates, has allowed a full range of support services to be provided to more than 150 companies internationally. Our success allows us to enjoy repeat business from our client base, coupled with strong referral recommendations due to our reliable and accurate service provision.
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Latest News

BSI Global partners with Medicom
Medicom has successfully renewed its contract for 2010 with BSI Global to provide public and in-house medical device training courses in United Kingdom. Medicom will also provide support in advising BSI on its Global strategy to acquire a position of dominance in providing training services to the medical device industry worldwide.
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Smithers UK (formally RAPRA) partners with Medicom
Medicom has successfully renewed its contract for 2010 with iSmithers to provide bespoke training for medical device polymer suppliers
 
DS Certificering A/S partners with Medicom
Medicom successfully renews contract for 2010 with DS Certificering A/S to provide public and in-house medical device training courses in Denmark.

Meet The Team

  • Poul Schmidt-Andersen
    Has spent 17 years in the fields of R&D and marketing of medical devices for Simonsen & Weel AS. As chief engineer he was responsible for all R&D...

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Our Services

Public Training Courses

Book now to secure your place on our remaining public training courses in 2010 at BSI London, UK.

Process Validation
09/03/2010
Chiswick, London

Process Validation
08/06/2010
Chiswick, London

Device Design
09/06/2010
Chiswick, London

QS Regulation
10-11/06/2010
Chiswick, London

QS Regulation
7-8/09/2010
Chiswick, London

Process Validation
15/09/2010
Chiswick, London

Device Design
16/09/2010
Chiswick, London

QS Regulation
1-2/12/2010
Chiswick, London

Process Validation
07/12/2010
Chiswick, London

Device Design
08/12/2010
Chiswick, London

Book now to secure your place on our remaining public training courses in 2010 at iSmithers, UK.

Medical Device Legislation and Material Selection

29-30 June

Shawbury, Shropshire, UK.

5-6 October

Shawbury, Shropshire, UK.

Book now to secure your place on our remaining public training courses in 2010 at DS Certificering, Copenhagen, Denmark.

Process Validation

18 May
Copenhagen, Denmark

Medical Device Design and Development Control

19 May
Copenhagen, Denmark

Establishing Compliance With ISO 11135-1:2007 for Validation of Ethylene Oxide Sterilization

12 October
Copenhagen, Denmark

 

Links & Downloads

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