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International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use
Results: 311

#	Item
251	Microsoft Word - 1_ICH_ICSR_Implementation_Guide_v5_01.docx Add to Reading List Source URL: www.fda.gov Language: English Software engineering Drug safety Pharmacology Computer programming Standards MedDRA International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Specification Ada Computing Clinical research Pharmaceuticals policy
252	INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE ICH HARMONISED TRIPARTITE GUIDELINE Add to Reading List Source URL: private.ich.org Language: English - Date: 2006-03-06 03:47:53 Health Clinical research Pharmaceutical industry Drug safety Pharmacy Pharmacovigilance Adverse effect Adverse event Serious adverse event Pharmacology Pharmaceutical sciences Medicine
253	PDF Document Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Pharmaceuticals policy Health Pharmaceutical industry Drug discovery Clinical trial International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Regulatory requirement Food and Drug Administration Pharmaceutical sciences Clinical research Research
254	ICH CTD General Q&A (from series #[removed]May-July Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 05:07:13 Clinical research Health Drug safety Pharmaceutical industry Design of experiments Clinical trial International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Food and Drug Administration Pharmacovigilance Pharmaceutical sciences Pharmacology Research
255	ICH CTD General Q&A (from series #[removed]May-July Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 05:07:25 Science Common Technical Document Drug discovery Pharmaceutical industry International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use M4 carbine Clinical trial Clinical research Research Clinical Data Management
256	Common Technical Document – Quality Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 05:07:15 Pharmacology Pharmaceutical sciences Validation Drug Master File Common Technical Document International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use HTML element Substance abuse Clinical trial Clinical research Pharmaceutical industry Research
257	CTD General Q&As June[removed] Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 05:07:22 Health Clinical Data Management Medical informatics Pharmaceuticals policy Pharmaceutical industry Electronic Common Technical Document Common Technical Document International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Marketing authorization Clinical research Medicine Research
258	GUIDELINE FOR GOOD CLINICAL PRACTICE Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 05:07:25 Clinical research Drug discovery Pharmacy Clinical Data Management Common Technical Document Clinical pharmacology Safety pharmacology International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Nonclinical studies Pharmacology Pharmaceutical sciences Research
259	Guidance for Industry E2B(M): Data Elements for Transmission of Individual Case Safety Reports: Questions and Answers Add to Reading List Source URL: www.fda.gov Language: English Clinical research Pharmaceutical industry Drug safety Pharmaceuticals policy Food and Drug Administration Clinical trial International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmaceutical sciences Pharmacology Research
260	Guidance for Industry E2C Clinical Safety Data Management: Periodic Safety Update Reports for Marketed Drugs Add to Reading List Source URL: www.fda.gov Language: English Medicine Pharmaceuticals policy Clinical research Drug safety Pharmaceutical industry Pharmacovigilance Regulatory requirement Food and Drug Administration International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmaceutical sciences Pharmacology Health