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Quality by Design
Results: 488

#	Item
231	Office of Pharmaceutical Quality Robert Iser Associate Director for Policy Development (acting), OPS Member OPQ Transition Team & OPF Transition Sub-Team June 24th, 2014 Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Clinical research Quality by Design Food and Drug Administration Quality management system Quality assurance Validation Pharmaceutical sciences Pharmaceutical industry Quality
232	ISSN 1520-295X System Performance Under Multi-Hazard Environments by Add to Reading List Source URL: mceer.buffalo.edu Language: English - Date: 2008-06-25 15:55:46 Occupational safety and health Seismology Software quality Reliability engineering Design for X Earthquake engineering Social vulnerability Emergency management Disaster Engineering Management Risk
233	Strategies for Clinical Investigators to Build Quality into Device Research Presented by Donna Headlee, RN BSN CCRP Consumer Safety Officer Division of Bioresearch Monitoring Office of Compliance Add to Reading List Source URL: www.fda.gov. Language: English Food and Drug Administration Science Clinical trial Design of experiments Pharmacology Pharmaceutical sciences Z Clinical investigator Logarithm Clinical research Pharmaceutical industry Research
234	Pharmaceutical Development: ICH Q8/Q(8)R Moheb M. Nasr, Ph.D.. Office of New Drug Quality Assessment Center for Drug Evaluation and Research (CDER) Food and Drug Administration (FDA) Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 04:06:23 Clinical research Management Quality Quality by Design Pharmaceutical sciences
235	ICH Q9 – An Industry Perspective: Ensuring Quality to Patients in a Risk-Based Regulatory Environment Thomas Schultz, Ph.D. Director, Regulatory Sciences Johnson & Johnson Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 04:07:07 Ethics Risk Risk management Information technology management Risk analysis Regulatory requirement IT risk Quality by Design Management Actuarial science Security
236	Implementation of ICH Q8, Q9, Q10 Breakout D : Pharmacopoieal Requirements and the New ICH Quality Paradigm – Time for a Change? Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 04:05:51 International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmacopoeia Kuala Lumpur Alternative medicine Software development process Process analytical technology Form Research Quality Quality by Design Science
237	US EPA REGION 9 AIR QUALITY TRENDS, [removed]HOUR SULFUR DIOXIDE (SO2) DESIGN VALUES BY DESIGNATED AREA* 1800 Concentration (ppb) Add to Reading List Source URL: www.epa.gov - Date: 2013-10-23 13:46:04
238	Office of Pharmaceutical Quality Robert Iser Associate Director for Policy Development (acting), OPS Member OPQ Transition Team & OPF Transition Sub-Team June 24th, 2014 Add to Reading List Source URL: www.fda.gov. Language: English Pharmacology Clinical research Quality by Design Food and Drug Administration Quality management system Quality assurance Validation Pharmaceutical sciences Pharmaceutical industry Quality
239	Workshop on Implementation of ICH Q8/Q9/Q10 and Other Quality Guidelines Beijing December 2008 Q11 Update Brian Withers, Abbott (United Kingdom) Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 04:06:26 Quality Quality by Design Quality management system
240	CDER Regulatory Applications – Investigational New Drug and New Drug Applications Add to Reading List Source URL: www.fda.gov Language: English Quality by Design Design for X Management Quality control Pharmaceutical industry Process analytical technology Product lifecycle management Quality Business Technology

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