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(147)
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It is appropriate that the Commission facilitates, to the extent possible,
access to testing and experimentation facilities to bodies, groups or laboratories established
or accredited pursuant to any relevant Union harmonisation legislation and which fulfil tasks in
the context of conformity assessment of products or devices covered by that Union harmonisation
legislation. This is, in particular, the case as regards expert panels, expert laboratories and
reference laboratories in the field of medical devices pursuant to Regulations (EU) 2017/745 and
(EU) 2017/746.
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