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Other links at Business Services > Consulting > Medical and Life Sciences > Regulatory Affairs |
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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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Pensa Technology Solutions Inc.
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21 cfr part 11 regulatory compliance of FDA pharmaceutical GMP validation for ERP life sciences computer information systems.
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Innovative Consultancy Services
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We are an Indian pharmaceutical consultant company established in the year 1998 and providing services in regulatory affairs, pharmaceutical dossiers, product/process development, and validation services.
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