Medicom Consulting

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Medicom have provided direct services to more than 150 client companies, below is a partial listing of some of our clients.

3M UK Darlington, UK
Abbott Vascular, Clonmel, IRL
Abbott Diagnostics IRL
Advanced Surgical IRL
Aerogen IRL
Aesculap AG GER
Allergan, Westport IRL
Axis Shield UK
B Braun Hospicare IRL
B. Braun UK
Beckman Coulter IRL
Becton Dickinson IRL, UK, SWEDEN, SINGAPORE
Benchmark IRL
Biocompatibles UK, U.S.
Biomet Merck UK
Biosil Ltd UK
Biotrin International Ltd IRL
BMR IRL
Boston Scientific, IRL, Netherlands
bsigroup UK
Cannon Avent UK
Celestica UK
Clearstream Technologies IRL
Clement Clarke International UK
Contamac UK
Cook Ireland IRL
Corin Medical UK
Creganna Medical Devices IRL
DCA Design Intn'l Ltd. UK
De Royal IRL
Depuy IRL
Depuy Leeds UK
Essilor France
Esterline Germany
Femcare UK
General Physics UK

 Watt Gilchrist UK
Gyrus UK
Harmac IRL
Hovione Portugal
Integra Neurosciences UK, IRL, USA
Interplex UK
Henkel Loctite Ireland Ltd. IRL
Lombard Medical UK
MediPlus Ltd UK
Medlogic UK
Merit Medical UK
Millipore IRL
Molnlycke Sweden, Belgium, Mexico, Finland, Thailand, U.S.
Nice Pak PDI UK
Organon Teknika IRL
Orgenics Israel
Owen Mumford Ltd UK
Pall Medical UK
Randox IRL
iSmithers (formally RAPRA) UK
Renishaw UK, IRL
Rottapharm IRL
Runfold Medical UK
S3Group IRL, Poland
Safety First Aid UK
Sauflon UK
SFML UK
Solvay  Netherlands
Spiegelberg Germany
Sterling Medical UK
Stryker IRL
The Brown Group UK
The Technology Partnership UK
The Tech Group IRL
Thermofisher UK
Tissuemed UK
USF Elga UK
Vistakon IRL
Vitalograph Ireland Limited IRL
Vysera IRL
Welch Allyn Limited IRL
 

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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