Medicom Consulting

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We help our clients in providing support solutions in a very broad range of activities, the list below is indicative of the range of skills and experience we can bring to your operations. We can tailor a solution to meet your individual needs in attaining operational excellence. 


New Facility Quality Systems Establishment

We have partnered successfully with several client companies to establish quality systems in new facility setups. This includes establishment of the top level Quality Manual and Quality System Procedures, product manufacturing, inspection and testing methods, and certification of quality systems by Notified Bodies. (Refer to our case study section)


FDA Form 483/Warning Letter Management

We have extensive experience and success in helping companies ensure all responses to inspection citations by FDA clearly provide evidence that the problems were understood, and that lasting and effective solutions have been put in place. We work with local management to correct the problems, and ensure that adequate documentary evidence of correction is included in responses to FDA. This process ensures timely and efficient review by FDA, thereby avoiding additional questions, and the avoidance of subsequent warning letters and import alerts


Process Validation

In addition to our training and auditing services we can provide independent review and comment on the adequacy of the correct approach to process validation activities. Many companies have taken advantage of this service prior to the execution of process validation work (Refer to our case study section)

 

Sterilization Validation

We have the expertise to provide objective and critical reviews of terminal and aseptic sterilization processes. We have worked successfully on Ethylene Oxide, Steam, Gamma and EBeam sterilization with various companies. In addition we have also handled satisfactorily responses to FDA on sterilization validation and control issues arising from difficult inspections. (Refer to our case study section)

 

Software Validation

In addition to our training and auditing services we can bring software expertise to support local management in quality improvement and validation activities. Support can be provides for both medical device software (embedded) and quality system control software. (Refer to our case study section)

 

Design Control

Existing clients have requested us to participate in design reviews and to provide independent review and comment on the adequacy of design verification and validation activities, including risk analysis, prior to the execution of such work and its submission to regulatory agencies.

 

Product Submissions (510(k), PMA & Technical Files)

We assist in the preparation of product submissions for medical device approval, and preparation of manufacturing facilities for PMA inspection. We have conducted this work for a broad range of devices including sterile disposables and electromechanical devices.

 

Project Management

We understand that in many situations the range of activities required to deliver on a major project such as a new facility start up requires excellent project management. We have worked successfully with project mangers on new facility start ups and have our own expertise to apply in particularly large projects, to ensure operational excellence is attained.

 

Mentoring

Our team of highly skilled and experienced professionals can offer clients valuable & impartial advice on a broad range of activities and thus provide a different perspective on how best to drive results and ensure business success, through operational excellence.


Our diverse mix of backgrounds and skill-sets ensures that the best advice & guidance on both general management & more specialised areas can be provided by our mentoring service.


Mentoring has always been a key requirement of any aspiring business. In light of current economic conditions the need for such a business offering has gained in importance and never been as apparent. With many businesses experiencing significant difficulties at present, Medicom is equipped to provide the necessary guidance & support to overcome quality and regulatory challenges.

Contact us for for more details

 

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


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