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Regulator Wall Clock
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Welcome to Regulator Watch
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Regulatory Affairs
Regulatory Affairs Consultants (RAC) Netherlands provides RA services to the pharmaceutical/biotech industry on European Drug Regulatory Procedures. Our services range from the pre-marketing authorisation application (MAA) phase to the post-MAA phase, including the application for reimbursement (in the Netherlands). 2011 kvk 51648180 e-mail: vandenberg@RA-consultants.nl. Powered by Dutch Web Promotion.
Regulatory Affairs | A relentless ambition to exceed your expectations.
Skip to main content. A relentless ambition to exceed your expectations. Our full range of Regulatory Affair solutions and services are dedicated to delivering the highest quality support, assistance and regulatory approvals for each of our clients utilizing fast, efficient, and cost-effective working practices. Adapting instantly to changing circumstances, quick and pragmatic, client-led regulatory/ commercial decisions ensure the degree of efficiency.
Regulatory affairs regulatory consulting services Poland
Pharmaceutical regulatory affairs services Poland and EU. Our company consists of people with high practical experience in EU regulatory affairs gained in Polish Authority and consulting companies therefore we are able to help you with smooth marketing authorization of medicinal products, medical devices or food supplements and with all processes related to maintenance of marketing authorization (variations, renewals etc.) as well as with any other regulatory affairs issues in Poland and in Europe.
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Regulatory Analysis & Benefit Valuation - Lisa A. Robinson
Lisa A. Robinson. Lisa A. Robinson specializes in assessing the costs, benefits, and other impacts of environmental, health, and safety policies and regulations. She has substantial experience in conducting these assessments, developing related methods, and drafting guidance documents. Please use the links above for more information on her qualifications and publications.
