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Search Results for 'New Phs Human Subjects And Clinical Trials Information Form'
Managing Sponsorship
tatiana-dople
ClinicalTrials.gov at
jane-oiler
Analysis of Current Competitiveness and Cost-Effectiveness to Select the Host Country
trish-goza
Regulatory issues in HIV cure Research
debby-jeon
UC DAVIS OFFICE OF RESEARCH
olivia-moreira
“ 28,424 cases of Ebola and still counting—what have we learned?”
mitsue-stanley
Impact of E9 Addendum to Industry
natalia-silvester
Manuscript Submission and Review:
cheryl-pisano
Clinical Trial Disclosure and Redaction:
yoshiko-marsland
Which Projects Do – and do Not – Require IRB Review?
kittie-lecroy
1 The Responsible Conduct
celsa-spraggs
Manuscript Submission and Review:
tatyana-admore
Manuscript Submission and Review:
sherrill-nordquist
Manuscript Submission and Review:
yoshiko-marsland
PRE-STRATIFIED RANDOMIZATION IS NOT NECESSARY FOR LARGE CLI
min-jolicoeur
Drug Development : Basic
myesha-ticknor
The Scientific Case Against Animal
liane-varnes
Performance in Initiating and Delivering Clinical Research
celsa-spraggs
Research on the Medicinal Uses of Cannabis
briana-ranney
European Clinical Trial Regulation
danika-pritchard
How to Find and Participate in a GIST clinical trial
natalia-silvester
© HRP Consulting Group Investigator Responsibilities in Human Subjects Research
liane-varnes
Topics in Clinical Trials (2
celsa-spraggs
Ethical issues in disclosing AD biomarker results
natalia-silvester
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