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Other links at Business Services > Consulting > Medical and Life Sciences > Regulatory Affairs |
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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.
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Medical Devices Consulting
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Regulatory affairs, quality assurance, custom software, and compliance contracting and consulting services.
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AQA
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Offering ISO 13485 and FDA QSR (21 CFR 820) Quality Manual and Operational Procedures and forms. Free software demo downloads available.
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CMAC Consultancy
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implementation, project administration and commissioning, as well as, IT services/operation management.
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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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