<--- Back to Details
First PageDocument Content
Pharmaceutics / Science / Design of experiments / Pharmacology / Clinical trial / Serious adverse event / Adverse event / Institutional review board / Regulatory requirement / Clinical research / Pharmaceutical industry / Research
Date: 2012-06-06 06:50:59
Pharmaceutics
Science
Design of experiments
Pharmacology
Clinical trial
Serious adverse event
Adverse event
Institutional review board
Regulatory requirement
Clinical research
Pharmaceutical industry
Research

Add to Reading List

Source URL: globalhealthtrials.tghn.org

Download Document from Source Website

File Size: 952,50 KB

Share Document on Facebook

Similar Documents

Jammu & Kashmir State Electricity Regulatory Commission Tariff Order on Annual Revenue Requirement

DocID: 1vcKs - View Document

Jammu & Kashmir State Electricity Regulatory Commission Order related to Review Petition on Annual Revenue Requirement

DocID: 1uns1 - View Document

Beneficial Ownership Requirements Overview Effective May 11, 2018 all non-exempt business clients will be required, due to a regulatory requirement, to provide Country Club Trust Company with certain information on Benef

DocID: 1ulOy - View Document

University of Pennsylvania  Institutional Review Board O Is IRB Review Required? The first question one should consider when assessing the requirement for IRB review is whether the activity meets the regulatory defini

DocID: 1tsSK - View Document

Economy / Financial services / Finance / Bank regulation / Systemic risk / Financial regulation / Banking / Basel II / Systemically important financial institution / Capital requirement / Basel Committee on Banking Supervision / Basel I

Regulatory Consistency Assessment Programme (RCAP) - Assessment of Basel III G-SIB framework and review of D-SIB frameworks - China

DocID: 1r9I5 - View Document