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Other links at Business Services > Consulting > Medical and Life Sciences > Regulatory Affairs |
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Pharmalink Consulting
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For all European regulatory affairs issues - CTA/IMPD submissions, regulatory compliance issues, and CMC
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Q-NET LLC
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EU authorized representative service in accordance with the EU medical device directive and EU machinery directive. Also act as FDA US agent for foreign establishments.
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Medical Device Consultants, Inc. (MDCI)
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provides worldwide regulatory, clinical, and quality assurance consulting services to medical device and diagnostic product manufacturers to meet US, Canadian, and European requirements.
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