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Pharmacology / Pharmaceutical sciences / Science / Pharmaceuticals policy / Quality / International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use / Electronic Common Technical Document / MedDRA / Quality by Design / Clinical research / Research / Pharmaceutical industry


Microsoft Word - ICH SC Summary Chicago 2006 Draft 3 with links.doc
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Document Date: 2012-06-21 10:46:44


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File Size: 45,11 KB

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City

Belgium Yokohama / Brussels / Chicago / /

Company

Global Cooperation Group / Pharmacopoeial Discussion Group / MSSO / ICH Controlled Terminology Working Group / Gene Therapy Discussion Group / CIOMS Working Group / Biotechnology-Derived Pharmaceuticals / /

Continent

Europe / /

Country

Japan / United States / China / /

Event

Business Partnership / FDA Phase / /

IndustryTerm

pharmaceutical development / chemical experts / treatment of cancer / prescription drug products / therapy products / pharmaceutical quality / /

MedicalCondition

non-rodent chronic study duration / cancer / chronic testing duration / /

MedicalTreatment

gene therapy / oncology therapies / /

Organization

WHO Regional Office for the Eastern Mediterranean / Maintenance and Support Services Organisation for MedDRA / World Health Organization / ICH Secretariat / WHO UMC / Uppsala Monitoring Centre / International Organisation for Standardisation / Bacterial Endotoxins Chapter / International Federation of Pharmaceutical Manufacturers and Associations / General Chapter on Color / FDA / Brussels SC / MedDRA Management Board / Association of Southeast Asian Nations / European Committee for Standardisation / European Union / ICH STEERING COMMITTEE / Asia-Pacific Economic Cooperation / Council for International Organizations of Medical Sciences / /

Position

Chair / representative / General / /

Product

SC / R2 / R1 / E2B(R) / SMQs / E2B / /

ProvinceOrState

South Carolina / /

PublishedMedium

the WHO / the Chicago / /

Technology

pharmacogenetics / Biotechnology / /

SocialTag