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Other links at Business Services > Consulting > Medical and Life Sciences > Regulatory Affairs |
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Octagon Research
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Using an electronic submission system (eSub), Octagon assists clients in the achievement an approved regulatory submission.
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Pharmalink Consulting
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For all European regulatory affairs issues - CTA/IMPD submissions, regulatory compliance issues, and CMC
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Consulting and active assistance in registration (regulatory affairs) and clinical trials of medicinal products, API's, supplements, and medical devices in CIS countries (Ukraine, Russian Federation, Kazakhstan, Moldova, Byelorussia).
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ERA Consulting Group
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Specialist services for pharmaceutical companies in regulatory affairs, including the development/registration of biotechnology and biological medicinal products, with offices in Europe and the United States.
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