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Top > Consulting > Medical and Life Sciences > Regulatory Affairs
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Regulatory affairs consultants based in the Washington DC metro area with the industry and FDA expertise to aid small to large pharmaceutical and medical device companies.
Date Added: Aug 5, 2008 Hits: Rating: 0.00 Votes: 0
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Compliance services to the Pharmaceutical / Biotechnology sector. Primarily assist organisations in the CSV field satisfy Regulatory and Compliance requirements. IVL has extensive field knowledge in the implementation of compliance solutions.
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Visitor Ratings Google PR 53. AQA
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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FDA inspections, vendor and clinical trial site audits, statistical services, clinical trial design/review, and preparation of responses to FDA compliance actions.
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Visitor Ratings Google PR 55. 21 CFR Part 11
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Visitor Ratings Google PR 56. MedFO, Inc.
Specialty consulting firm that focuses almost exclusively upon the strategy, operations, and functions of departments that fall under the Medical Affairs umbrella.
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Carexa's experienced consultants provide strategy and services for drug development and regulatory affairs.
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Octagon offers a comprehensive suite of services that span the entire clinical research and development lifecycle.
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UK based regulatory affairs consultants offering a wide range of services to international companies in the pharmaceutical, medical device, nutritional and healthcare industry.
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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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