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Science / Common Technical Document / Pharmaceutical industry / Evaluation methods / Clinical trial / Electronic Common Technical Document / International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use / Clinical research / Research / Clinical Data Management


-- Bert spiker, PhD, MD SENIOR VICE PRESIDENT SClENl.lflC AND REQUIATORY AFFAIRS .*
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Document Date: 2000-11-15 00:43:10


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File Size: 1,22 MB

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Company

ICH Global Coordination Group / ITT / /

Continent

America / /

Country

Japan / United States / /

Currency

USD / /

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IndustryTerm

comparability protocols / anti-infective products / process validation protocol / biotechnology / pharmaceutical / pharmaceutical products / drug product / research-based pharmaceutical / biopharmaceutical studies / /

MedicalCondition

animal infection / disease / /

Organization

Organization of the Common Technical Document / European Union / Food and Drug Administration / ICH Steering Committee / /

Person

Lona Term Efficacv / /

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Position

author / SENIOR VICE PRESIDENT SClENl.lflC AND REQUIATORY AFFAIRS / General / /

Product

M-16 / /

ProvinceOrState

Maryland / /

Technology

pharmacokinetics / comparability protocols / process validation protocol / drug development / biotechnology / /

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