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Beskrivelse: QUADRAS ist Ihr Dienstleister bei allen Fragen zur Zulassung und Registrierung von Medizinprodukten weltweit. Die folgenden Seiten enthalten Informationen zu unseren Dienstleistungen für die Märkte in Europa, Deutschland ...
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Consultoria tecnologias sanitarias, ayudamos a los fabricantes a obtener el marcado CE, implantar sistemas de gestion de calidad segun ISO13485 y actuamos de ...
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Medical Device Forum. QSR - GMP contracting and consulting services for the medical device industry. Services include regulatory affairs, quality assurance, custom ...
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TopPharm: Pharmaceutical regulatory affairs and regulatory consulting services in Poland and EU. We are former authority experts.
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New Drug Approvals provides regulatory affairs consulting services to the pharmaceutical and related industries in an efficient and cost-effective manner
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Industrial and regulatory know-how not only to preclude FDA issues but also to solve tough scientific, clinical & regulatory issues which may arise pre & ...
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HIPAA training - We provide online HIPAA compliance training and HIPAA hitech training for privacy and security rules for covered entities and business associates ...
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Regulatory compliance and validation documentation consulting for FDA-regulated drug manufacturing and testing companies worldwide.
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