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CTEP
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101	Phase 1 Single Agent Template X. ADVERSE EVENTS: LIST AND REPORTING REQUIREMENTS Adverse event (AE) monitoring and reporting is a routine part of every clinical trial. The following list of AEs (Section X.1) and the c Add to Reading List Source URL: ctep.cancer.gov Language: English - Date: 2008-05-28 21:39:37 Pharmaceutics Pharmaceutical sciences Adverse event Clinical trial Norfloxacin Clinical research Pharmaceutical industry Research
102	CTEP Grant: Human Services Career Cluster Advisory Committee List[removed]Stakeholder Category Name Add to Reading List Source URL: www.camdencc.edu Language: English - Date: 2013-01-29 15:40:08 Camden County College Cherry Hill New Jersey Garden State Athletic Conference Gloucester Township New Jersey Middle States Association of Colleges and Schools Camden New Jersey Rutgers–Camden London Borough of Camden Camden Camden County New Jersey Geography of New Jersey New Jersey
103	Microsoft Word - PPTP Overview[removed] Add to Reading List Source URL: ctep.cancer.gov Language: English - Date: 2014-08-03 16:10:27 Drug discovery Cancer organizations Pharmaceutical industry Pre-clinical development Neuroblastoma Glioblastoma multiforme Cancer research Medicine Oncology Brain tumor
104	MATERIAL TRANSFER AGREEMENT Add to Reading List Source URL: ctep.cancer.gov Language: English - Date: 2014-08-03 16:10:27 Cancer research Technology transfer Intellectual property law 96th United States Congress Bayh–Dole Act Point-to-Point Tunneling Protocol Patent Title 35 of the United States Code Health Medicine Technology National Institutes of Health
105	Date: May 17, 2010 Topic: CTEP Guidance: CTCAE v4.0 Grading Scales with Numeric Component From: CTEP, NCI Investigation Drug Branch CTEP has become aware of uncertainty regarding the grading of lab values using CTCAE v4. Add to Reading List Source URL: evs.nci.nih.gov Language: English - Date: 2010-05-17 11:14:05 Food science Health sciences Self-care Nutrition Anemia Knowledge Health Medicine Applied sciences
106	Specific Instructions for the Use of Organ Dysfunction Templates The goal of an organ dysfunction study is to define the dose of an agent associated with an acceptable toxicity profile and measurable pharmacokinetic para Add to Reading List Source URL: ctep.cancer.gov Language: English - Date: 2011-08-30 13:16:22 Piperazines Hepatotoxicity Toxicology Methadone Liver function tests Sepsis Norfloxacin Paracetamol toxicity Medicine Chemistry Hepatology
107	Specific Instructions for the Use of Organ Dysfunction Templates The goal of an organ dysfunction study is to define the dose of an agent associated with an acceptable toxicity profile and measurable pharmacokinetic para Add to Reading List Source URL: ctep.cancer.gov Language: English - Date: 2011-08-30 13:16:22 Piperazines Creatinine Methadone Chemistry Organic chemistry Norfloxacin
108	Community Transportation Enhancement Program Application Instructions September 2012 This is the official instruction set for submitting a Community Transportation Enhancement Program (CTEP) Application to MDT. Every eff Add to Reading List Source URL: mdt.mt.gov Language: English - Date: 2012-10-11 12:10:32 Pyridines Project manager Construction Project management Business Technology Alkynes CTEP Imidazoles
109	TEMPLATE INSTRUCTIONS The protocol template is a tool to facilitate rapid protocol development. It is not intended to supersede the role of the Protocol Chair in the authoring and scientific development of the protocol Add to Reading List Source URL: ctep.cancer.gov Language: English - Date: 2014-07-21 21:23:40 Pharmacology Health Cancer organizations Design of experiments Food and Drug Administration Cancer Trials Support Unit Clinical trial Regulatory requirement Methadone Clinical research Medicine Research
110	Glossary of Terms CTEP Operational Efficiency Working Group (OEWG) Version date: April 1, 2012 Add to Reading List Source URL: ctep.cancer.gov Language: English - Date: 2012-04-01 16:42:29 Pharmaceutical industry Case report form Pharmaceutics Pharmacology Clinical research Research Clinical Data Management