Medical Device & Quality Assurance
Consultancy
Compliance with the Essential Requirements of the Medical Device Directive (MDD 93/42/EEC)
is now mandatory........effective June 13th 1998............
Were you fully prepared.....?
If not, then M.D. & QA Consultancy can still help you prepare...
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Medical Device & QA Consultancy's wide experience of implementing Strategies covering all Classes of Device, enables us to offer a One Stop Source of all the COST EFFECTIVE help that you will ever need, to complement your own In-House effort and ensure a successful Medical Device Directive 93/42/EEC Compliance Strategyà
Our involvement in your Strategy can be Minimal /Strategic or Full Involvement...including any level in between. A Partnership Strategy package can be tailored to meet your exact requirements
If you need further information on how we can help you plan effectively, please make contact with us supplying the brief details requested on the
CONTACT US page, or by using the following Fax Number or E-mail Address, and someone will call you back to discuss your needs, in Total Confidence:+ 44 (0) 161 903 9787 or Tel: + 44 (0) 161 980 4310
e-mail: bernardt@mdqaconsultancy.co.uk
OR
e-mail: mdqaco@globalnet.co.uk
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OWN BRANDING of already CE Marked Products
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COMPANY PROFILE of Medical Device & QA Consultancyà
SUMMARY of Medical Device & QA Consultancy servicesà
TECHNICAL FILE summary of the content of the fileà
CONFORMANCE routes, full list of Quality System and Type Test possible choicesà
CHECKLIST of 93/42/EEC issues to addressà
AUTHORIZED REPRESENTATIVE MDD 93/42/EEC services for Companies located outside Europeà
CONTACT US details of Medical Device & QA Consultancy's contacts
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