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Other links at Business Services > Consulting > Medical and Life Sciences > Regulatory Affairs |
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Validation and cGMP Compliance
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Equipment and Software Validation. Part 11 of 21 CFR Compliance. Regulations, cGMP, Validation knowledge base. FDA Warning letters.
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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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FDALive.com
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Live broadcasting of FDA meetings via video-conferencing, webcasting and audio-conferencing. Post-meeting webcasts, DVD, CD's, videotapes and transcripts available.
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Solutions MDI, Inc.
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clinical affairs, quality systems, compliance strategies, CE mark and FDA submissions.
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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.
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