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Consulting and active assistance in registration (regulatory affairs) and clinical trials of medicinal products, API's, supplements, and medical devices in CIS countries (Ukraine, Russian Federation, Kazakhstan, Moldova, Byelorussia).
Date Added: Jul 19, 2006 Hits:
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| 333. |
R. A. Q .A. Associates
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R.A.Q.A. Associates provides FDA and ISO related consulting services to medical device and pharmaceutical companies. We specialize in helping firms with regulatory and cGMP problems, constructing and implementing entirely new quality and regulatory systems or improving existing systems.
Date Added: Jul 19, 2006 Hits:
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| 334. |
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.
Date Added: Jul 19, 2006 Hits:
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| 335. |
PAT toolkit
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Provides information on the FDAa£á?s Process Analytical Technology (PAT) Initiative and outlines a software package to help pharmaceutical manufacturers implement this initiative.
Date Added: Jul 19, 2006 Hits:
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| 336. |
Quality Vectors
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Provide validations, cGxP compliance, systems engineering, and quality systems to pharmaceutical, medical device, and biotechnology industries.
Date Added: Jul 19, 2006 Hits:
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