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Common Technical Document
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491	PDF Document Add to Reading List Source URL: www.fda.gov Language: English Clinical Data Management Food and Drug Administration Drug safety Pharmaceutical industry Electronic Common Technical Document Investigational New Drug New Drug Application Common Technical Document Electronic submission Research Clinical research Medicine
492	PDF Document Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2013-06-24 11:44:53 Pharmaceutical industry Health Canada Medical informatics Electronic Common Technical Document Common Technical Document Health Products and Food Branch Clinical Data Management Research Clinical research
493	Storage Management Technical Specification, Part 2 Common Profiles Version 1.3.0, Rev 6 This document has been released and approved by the SNIA. The SNIA believes that the ideas, methodologies and technologies described Add to Reading List Source URL: www.snia.org Language: English - Date: 2011-03-20 07:19:30 Storage Management Initiative – Specification Reference Technical communication Storage Networking Industry Association Tagged Image File Format Distributed Management Task Force ISCSI Specification Computing Technology Computer storage
494	27 July 2011 EMA[removed]Transatlantic Administrative Simplification Action Plan – Final Report on implementation Under the auspices of the Transatlantic Economic Council, on 28 November 2007 the European Commissio Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:04:30 Pharmaceutical industry Pharmacology Clinical Data Management European Medicines Agency Food and Drug Administration Validation Pharmacovigilance Common Technical Document Pharmaceutical sciences Research Clinical research
495	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
496	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
497	D2.2 Standard document and validation common specifications Submission Date[removed]COMPETITIVENESS AND INNOVATION FRAMEWORK PROGRAMME Add to Reading List Source URL: www.eu-spocs-starterkit.eu Language: English - Date: 2013-01-04 04:01:27 Open formats Markup languages Technical communication PAdES XAdES CAdES Portable Document Format European Telecommunications Standards Institute XML Computing Computer file formats Cryptography standards
498	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
499	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
500	GUIDELINE FOR GOOD CLINICAL PRACTICE Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 05:07:15 Pharmaceutical sciences Research Dosage forms HTML element Validation Excipient Common Technical Document Pharmaceutical industry Pharmacology Clinical research

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