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Pharmaceutical Research
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#	Item
241	TAG Inventory Quality Guidelines version 2.1 Summary of Revisions The Trustworthy Accountability Group (TAG) Inventory Quality Guidelines (IQG) promote the flow of advertising budgets into digital advertising with indust Add to Reading List Source URL: tagtoday.net Language: English - Date: 2015-12-17 15:04:07 Pharmaceutical industry Validity Clinical data management Clinical research Quality Validation Advertising Professional certification
242	I Aver: Providing Declarative Experiment Specifications Facilitates the Evaluation of Computer Systems Research Ivo Jimenez and Carlos Maltzahn Jay Lofstead Add to Reading List Source URL: tinytocs.ece.utexas.edu Language: English - Date: 2016-03-05 17:06:25 Validity Pharmaceutical industry Measurement Psychometrics Reproducibility Scientific method Validation Declarative programming
243	Copernicus Land Monitoring Services Validation of CORINE Land Cover Products Summary of preliminary results 1. Context This document aims at covering the validation of CORINE Land Cover (CLC) data set, specifically the C Add to Reading List Source URL: land.copernicus.eu Language: English - Date: 2015-12-18 04:50:17 Pharmaceutical industry Validity Clinical data management Clinical research Quality Validation Coordination of Information on the Environment
244	BOOKS ABOUT M4 RIFLE SOP Cityhalllosangeles.com M4 RIFLE SOP Add to Reading List Source URL: m.cityhalllosangeles.com Language: English - Date: 2015-03-05 01:47:09 Pharmaceutical industry Clinical research Documents Good clinical practice Military terminology Standard operating procedure M4 carbine Procedure M4 SOP
245	Annex 2 to the HMA eSubmission Roadmap: Implementation of mandatory eCTD format for regulatory submissions (Status: Final version adopted by the eSubmission CMB. Dated 26 JulyScope This annex is intended for both Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:41 Clinical research Clinical data management Electronic common technical document Pharmaceutical industry Pharmaceuticals policy Marketing authorization Electronic submission
246	Office of the Vice-President, Research and Innovation Office of Research Ethics Add to Reading List Source URL: www.research.utoronto.ca Language: English - Date: 2016-05-16 14:45:05 Medical ethics Clinical research ethics Human subject research Professional ethics Pharmaceutical industry Research ethics Clinical research coordinator Informed consent Psychology Consent Ethics Debriefing
247	Stanford University HRPP Guidance General Requirements for Informed Consent Add to Reading List Source URL: researchcompliance.stanford.edu Language: English - Date: 2016-04-12 01:21:52 Clinical research Medical ethics Pharmaceutical industry Research ethics Clinical research coordinator Clinical trial Informed consent Human subject research
248	Updated 08 JulyRelease Notes Detailing the updates of the EU eCTD Module 1 Specification The published version 3.0 has been updated to versionto correct pick list values and the updated version was publishe Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:41 Clinical data management Clinical research Identifiers Universal identifiers Pharmaceutical industry Universally unique identifier Electronic common technical document Validation Globally unique identifier
249	ePCRN-IDEA2: An Agent-Based System for Large-Scale Clinical Trial Recruitment Seyi Feyisetan Gareth Tyson Add to Reading List Source URL: www.eecs.qmul.ac.uk Language: English - Date: 2012-05-30 06:42:01 Clinical research Clinical trials Design of experiments Pharmaceutical industry Clinical pharmacology Patient recruitment ClinicalTrials.gov Pharmacovigilance Health informatics Randomized controlled trial
250	 HOME STUDY The Evolving World of Metrics Are Performance Metrics About Doing the Right Things or Simply Doing Things Right? Add to Reading List Source URL: www.acrpnet.org Language: English - Date: 2016-07-29 11:46:01 Clinical research Pharmaceutical industry Drug discovery Process management Healthcare quality Clinical trial Performance metric Business process improvement Drug development Medical guideline Risk management Clinical Data Inc

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