Medical Device & QA Consultancy's
 Authorized Representative Services

                    

Please feel free to contact us by using either the Fax or e-mail details  here, or the Automatic Submission form below;

Contact: Bernard Tremaine               e-mail:  bernardt@mdqaconsultancy.co.uk

e-mail: info@mdqa.co.uk                Fax: +44 161 903 9787

An assurance is given that all information provided will be treated in the strictest confidence and will only be used to assess your needs and enable us to respond in the most effective way to your enquiry.

 AUTHORIZED REPRESENTATIVE ENQUIRY

  

 Your full name:  
 Company name:  
 State / Province / Area:  
 Country:  
 Email address:  
 Web Site address (if applicable):  

 The Nature of Your Business: eg manufacture, distribution etc  
 The Nature of Your Products:   


Which Quality System Standard are you currently Implementing ? Please Check all that apply.
  ISO 9001:1994                  ISO 9002:1994              ISO 9003:1994        ISO 9001:2000
  EN 46001:1996                 EN 46002:1996               EN 46003:1998
  ISO 13485:1996/2001      ISO 13485:2003              FDA QSR 820
 

About the Classification of your Product and your choice of Notified Body and Preferred Start Date. Please Leave these answers Blank if you are unsure about these questions or you have not yet chosen your Notified Body or if you do not yet have a Start date in mind.
 

 The class of your Products, ie: I, IIa, IIb or III or Unknown:  
 Your Preferred Start Date, should you decide to use Our Services  
 The Full Name and Job Title of the person who will Sign the Agreement  
 Your Intended Notified Body, if known:   





Please enter below any further details of the nature of your enquiry, giving as much information as possible.



Thank you for taking the time to fill out this enquiry form. Someone from Medical Device & QA Consultancy will get back to you as soon as possible, to discuss the most effective way to help you meet your needs.

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