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51. Medius AG - Drug Regulatory Affairs and Development



Medius is a consulting and service company based in Switzerland, engaged in regulatory affairs of pharmaceuticals, medical devices, and in vitro diagnostics.
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Date Added: Jul 19, 2006 Hits:

52. QuadraMed



A pharmaceutical regulatory company with european affiliated offices specializing in marketing authorizations, european clinical trials, mutual recognition procedures, and orphan drug designations.
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Date Added: Jul 19, 2006 Hits:

53. Compliance Associates - Life Science Software and Consulting Services



Compliance Associates is dedicated to providing the Life Science industry with solutions to complex regulatory and business critical requirements.
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Date Added: Jul 19, 2006 Hits:

54. FDACompliance.Net



Provides Members with searchable databases as well as full text searching of regulatory compliance topics.
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Date Added: Jul 19, 2006 Hits:

55. Medical device consultants



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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Date Added: Jul 19, 2006 Hits:

56. FDA Advisors with scientific and technical expertise



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.
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Date Added: Jul 19, 2006 Hits:

57. IDEC Validation Ltd



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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Date Added: Jul 19, 2006 Hits:

58. 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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Date Added: Jul 19, 2006 Hits:

59. Biologics Consulting Group- Regulatory Affairs Consultants for Manufacturers of biological products



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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Date Added: Jul 19, 2006 Hits:

60. 21 CFR Part 11



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Date Added: Jul 19, 2006 Hits:

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