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Other links at |
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Valid Ground
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Valid Ground offers services to cover most aspects of Good Clinical Practice compliance initiatives. We serve pharmaceutical, biotech, and medical device companies, academic institutions, institutional review boards, and contract research organizations.
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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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SMB Validation and Compliance Services Group
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SMB Group is designed to get your equipment into production promptly while ensuring that all regulatory requirements are systematically fulfilled with a minimum of interference with operations.
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Schell Associates
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Consulting services including regulatory affairs, preclinical and GLP testing, manufacturing, quality, compliance, and clinical studies.
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Medical device consultants
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Consultants for FDA and internationally regulated medical device firms, specializing in submissions, compliance, warning letter responses, inspection responses, quality system compliance, auditing and training
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