Distributed application - PDFSEARCH.IO - Document Search Engine

Distributed application
Results: 711

#	Item
631	Total Cost of Ownership An Important Piece of Any Sustainability Plan As with any development of education data systems, it is important to know and articulate what is needed for the ongoing support and maintenance of th Add to Reading List Source URL: nces.ed.gov Language: English - Date: 2014-04-28 16:47:22 Finance Microeconomics Costs Enterprise application integration Information technology governance Total cost of ownership Whole-life cost Data center Concurrent computing Distributed computing Computing
632	Cyber Security Beginners Guide to Firewalls A Non-Technical Guide Essential for Business Managers Office Managers Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 14:35:40 Computing Personal firewall Firewall Network security Internet security Application firewall Distributed firewall Computer network security Computer security Cyberwarfare
633	Guidance for Industry Manufacturing, Processing, or Holding Active Pharmaceutical Ingredients DRAFT GUIDANCE This guidance document is being distributed for comment purposes only. Add to Reading List Source URL: www.fda.gov Language: English Business Pharmaceutical sciences Validity Food safety Quality Validation Application programming interface Packaging and labeling Good manufacturing practice Pharmaceutical industry Pharmaceuticals policy Technology
634	Guidance for Industry Submitting Debarment Certification Statements DRAFT GUIDANCE This guidance document is being distributed for comment purposes only. Comments and suggestions regarding this draft document should be s Add to Reading List Source URL: www.fda.gov Language: English Health Pharmaceutical sciences Clinical research Drug safety Pharmaceuticals policy Debarment New Drug Application Investigational New Drug Drug Master File Food and Drug Administration Medicine Pharmaceutical industry
635	Guidance for Industry Providing Submissions in Electronic Format — Postmarketing Safety Reports DRAFT GUIDANCE This guidance document is being distributed for comment purposes only. Add to Reading List Source URL: www.fda.gov Language: English Research Adverse Event Reporting System Structured Product Labeling Center for Biologics Evaluation and Research New Drug Application Postmarketing surveillance Federal Food Drug and Cosmetic Act Food and Drug Administration Medicine Health
636	Guidance for Industry Applications Covered by Section 505(b)(2) DRAFT GUIDANCE This guidance document is being distributed for comment purposes only. Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Medicine Food and Drug Administration Drug safety New Drug Application Generic drug Drug Price Competition and Patent Term Restoration Act Federal Food Drug and Cosmetic Act Approved drug Pharmaceutical industry Pharmaceutical sciences Pharmaceuticals policy
637	Guidance for Industry Clinical Pharmacology Data to Support a Demonstration of Biosimilarity to a Reference Product DRAFT GUIDANCE This guidance document is being distributed for comment purposes only. Add to Reading List Source URL: www.fda.gov Language: English Clinical research Pharmaceutical industry Food and Drug Administration Biotechnology Biosimilar Biologic Validation Pharmacokinetics New Drug Application Pharmaceutical sciences Pharmacology Medicine
638	Guidance for Industry Postmarketing Safety Reporting for Human Drug and Biological Products Including Vaccines DRAFT GUIDANCE This guidance document is being distributed for comment purposes only. Add to Reading List Source URL: www.fda.gov Language: English Research Adverse Event Reporting System Center for Biologics Evaluation and Research Validation Regulatory requirement New Drug Application Biologic Center for Drug Evaluation and Research Postmarketing surveillance Food and Drug Administration Medicine Pharmaceutical sciences
639	Guidance for Industry ANDA Submissions — Content and Format of Abbreviated New Drug Applications DRAFT GUIDANCE This guidance document is being distributed for comment purposes only. Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Research Clinical research Pharmaceuticals policy Clinical Data Management Abbreviated New Drug Application New Drug Application Electronic Common Technical Document Generic drug Food and Drug Administration Pharmaceutical industry Medicine
640	Guidance for Industry Initial Completeness Assessments for Type II API DMFs Under GDUFA DRAFT GUIDANCE This guidance document is being distributed for comment purposes only. Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Health Pharmaceuticals policy Clinical research Drug Master File Food law New Drug Application Federal Food Drug and Cosmetic Act Generic drug Pharmaceutical industry Pharmaceutical sciences Medicine

UPDATE