Medicom Consulting

You are here  : Home News DS Certificering A/S partners with Medicom
DS Certificering A/S partners with Medicom Print E-mail
Medicom successfully renews contract for 2011 with DS Certificering A/S to provide public and in-house medical device training courses in Denmark.
 

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

downloads