'Scientifically appropriate' presentation slideshows

ClinicalTrials Update on Clinical Trial Registration and Results Reporting Requirements

ClinicalTrials.gov Update on Clinical Trial Registration and Results Reporting Requirements. Rebecca J. Williams, Pharm.D., MPH ClinicalTrials.gov June 22, 2009. 1. 1. History of ClinicalTrials.gov. FDAMA 113 (1997): Mandates Registry

542 views • 35 slides

Safe Substitution of Biologics

Safe Substitution of Biologics. What is automatic substitution?. 1) Physician writes a prescription. 2) Pharmacist is allowed, or required, to provide a different medicine to the patient. X. What Does The Law Say About Interchangeability?. Biologics Price Competition and Innovation Act ,

444 views • 23 slides

JCMT, UKIRT and Gemini Scheduling Workshop

JCMT, UKIRT and Gemini Scheduling Workshop. Day 1 Review. Agenda - Day 1. Session 1: UKIRT projects and plans. (Subaru) 08:45-09:00 Introduction and welcome - Nick Rees 09:00-09:45 Current ORAC project - Gillian Wright 09:45-10:30 Planned ORAC Scheduler - Alan Bridger

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246 views • 14 slides

Vulnerable Populations Subpart B Requirement for IRB to make Protocol Specific Determinations

Vulnerable Populations Subpart B Requirement for IRB to make Protocol Specific Determinations. AAHRRP Element II.4.A.

225 views • 14 slides

Office of Science Statement on Digital Data Management

Office of Science Statement on Digital Data Management. Basic Energy Sciences Advisory Committee Meeting March 1 st , 2013. Laura Biven, PhD Senior Science and Technology Advisor Office of the Deputy Director for Science Programs (SC-2) Laura.Biven@science.doe.gov.

220 views • 8 slides