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European Authorized Representative, Authorised Representative, EC REP, Medical Devices
Описание: Assists medical device manufacturers achieve European and/or FDA regulatory compliance; services encompass authorized representative issues.
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Analyzes client needs and develops solutions for third party administrators, insurance companies and self-funded plans to maximize savings and promote quality.
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RAA can help you get FDA approval. Contact Regulatory Affairs Associates.
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An information company that helps manage the cost, quality, and delivery of healthcare services and benefits.
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Consultancy providing clinical trials monitoring, report writing, training and medical affairs consulting.
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