Medicom Consulting

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Meet The Team
Tom Donnelly (Director) Print E-mail
Graduated in Microbiology from Queens University Belfast, and then worked for the healthcare industry in Ireland for thirteen years with Baxter Healthcare and National Medical Care.
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Ron Pagan (former Director) Print E-mail

After 15 years with Medicom Consulting, Ron finally retired and resiged his directorship in May of 2010. However, he provides general advice when needed on past projects and technical issues, and is available for some project work in 2011. We all wish him well in his retirement and extend our thanks for his contribution to the sucess of Medicom Consulting.


Ron, graduated in Mechanical Engineering from Queens University Belfast, and is a Chartered Engineer. He has international experience in the Engineering, Chemical, Textile and Medical Device industries, having worked in the UK, Germany, Belgium and Ireland for twenty-eight years, of which eleven were as Chief Executive, latterly of a US medical device manufacturers operation.

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Howard Beaumont Print E-mail
Graduated in Production Technology and Production Management from Aston University, Birmingham, where he worked in both project management and quality management within the automotive industry, before moving into the medical device sector.
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Aidan Madden Print E-mail

Aidan holds a BSc in Biochemistry and Microbiology, an MSc in Immunochemistry and a Diploma in Pharmaceutical Manufacturing Technology. In his 17 year career he worked in senior quality roles for pharmaceutical multinationals producing vaccines, sterile injections and solid dosage formulations. Aidan is also a qualified QP on a number of Manufacturing Authorisations in Ireland.

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Frank Enright Print E-mail

Frank is qualified with a Masters in Business Administration, a Degree in Manufacturing Technology, and is a Certified Lead Auditor.

His 17 years experience includes senior management roles in Regulatory Affairs, Quality Assurance and Operations within the Medical Device and Aerospace industries.

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Poul Schmidt-Andersen Print E-mail
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 efforts within the active medical devices field such cardiac output computers, neonatal monitoring, resuscitation and diathermy equipment.
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Euan Cameron Print E-mail

Following a period as a research scientist at the Tenovus Institute for Cancer Research in Cardiff, Wales, Euan ultimately becoming its Deputy Director.

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Dr Paul Shipton Print E-mail
Holds a first class honours and PhD in Polymer Technology from Brunel University London and has 27 years international experience in plastics materials use in product development and manufacturing and a trained Six Sigma Champion.
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David Harkin Print E-mail
A MBA qualified senior manager, mechanical engineer & managing consultant with 20 years manufacturing knowledge & experience at executive level in international companies, now primarily advising MDs/factory owners and business leaders on performance improvement.
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Latest News

Regulatory Updates

Two new guidance documents on Clinical Investigation: MEDDEVs 2.73/3 & 2.7/4

14-12-2010

FDA CDER (&CBER & CVM) Guidance for Industry: Process Validation: General Principles and Practices

24-11-2011

FDA CDRH: Medical Device Innovation Initiative

February 2011


 
Our 2010 Success

Although the 2010  economy was a difficult year for many businesses, we can look back with justified pride in our success and draw confidence that we can improve and grow our services to the health care industry in 2011, nationally and internationally.

Here are some brief statistics on our 2010 activities, which are indicative of our ongoing success

  • we provided major services to more than 24 medical device and drug facilities
  • we agreed service contracts with 12 new companies
  • we trained over 250 people in the industry, including Competent Authority personnel
  • we successfully project managed 3 FDA compliance inspections in the UK and China

 
Smithers UK (formally RAPRA) partners with Medicom
Medicom has successfully renewed its contract for 2011 with iSmithers to provide bespoke training for medical device polymer suppliers

 
DS Certificering A/S partners with Medicom
Medicom successfully renews contract for 2011 with DS Certificering A/S to provide public and in-house medical device training courses in Denmark.


Public Training Courses

Ireland

Book now to secure your place on our remaining public training courses in 2012

QS Regulation

11-12 June, Limerick, Ireland

Process Validation

13-14 June, Limerick, Ireland

Process Validation

16-17 October, Ireland

QS Regulation

23-24 October, Limerick, Ireland

United Kingdom

Book now to secure your place on our remaining public training courses in 2012 at Smithers RAPRA, Shawbury, Shropshire, UK.

QS Regulation

3 July,

Process Validation

4 July

Medical Device Design & Development

5 July

Denmark

Book now to secure your place on our remaining public training courses in 2012 at DS Certificering, Copenhagen, Denmark.

Process Validation

Dates to be confirmed soon

Medical Device Design and Development Control

Dates to be confirmed soon

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

Dates to be confirmed soon


Links & Downloads

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