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#	Item
621	Guidance for Industry: Changes to an Approved NDA or ANDA Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical industry Pharmaceutical sciences Pharmaceuticals policy Clinical research Food law New Drug Application Federal Food Drug and Cosmetic Act Validation Center for Drug Evaluation and Research Food and Drug Administration Medicine Health
622	Guidance for Industry Changes to an Approved NDA or ANDA Questions and Answers U.S. Department of Health and Human Services Add to Reading List Source URL: www.fda.gov Language: English Medicine Health Pharmaceuticals policy Clinical research Food law Drug Master File New Drug Application Good manufacturing practice Center for Drug Evaluation and Research Pharmaceutical industry Food and Drug Administration Pharmaceutical sciences
623	Guidance for Industry: Changes to an Approved NDA or ANDA Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical industry Pharmaceutical sciences Pharmaceuticals policy Clinical research Food law New Drug Application Federal Food Drug and Cosmetic Act Validation Center for Drug Evaluation and Research Food and Drug Administration Medicine Health
624	Guidance for Industry Changes to an Approved NDA or ANDA Questions and Answers U.S. Department of Health and Human Services Add to Reading List Source URL: www.fda.gov Language: English Medicine Health Pharmaceuticals policy Clinical research Food law Drug Master File New Drug Application Good manufacturing practice Center for Drug Evaluation and Research Pharmaceutical industry Food and Drug Administration Pharmaceutical sciences
625	Guidance for Industry ANDA Submissions — Content and Format of Abbreviated New Drug Applications DRAFT GUIDANCE This guidance document is being distributed for comment purposes only.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
626	Eesti Tubaka ja Alkoholikahjude Vähendamise Koda (ETAK) taunib avalikus kohas alkoholi joomise lubamist. Noortele ei tohi anda sõnumit, et alkoholi tarvitamine on meie ühiskonnas sallitav ja normaalne. Hiljuti Valitsu Add to Reading List Source URL: www.arstideliit.ee Language: Estonian - Date: 2014-06-06 17:17:42
627	Enska þýðingin á stefnunni - frá þýðanda[removed]01_VERSION 2 Add to Reading List Source URL: eng.fjarmalaraduneyti.is Language: English - Date: 2010-11-09 05:39:39 Technology Procurement Environmental economics Government procurement E-procurement Ecolabel Purchasing Environmental resources management Sustainable procurement Business Supply chain management Systems engineering
628	Den femte europeiska undersökningen om arbetsvillkor Sammanfattning Inledning Arbete spelar en viktig roll i människors liv, liksom för företag och samhället som helhet. EU har ända sedan det Add to Reading List Source URL: www.eurofound.europa.eu Language: Swedish - Date: 2013-12-23 15:28:23
629	TIP KESELAMATAN Melindungi document anda, workbook, atau presentation dengan kata laluan, kebenaran dan sekatan lain In Microsoft Office, you can use passwords to help prevent other people from opening or modifying your Add to Reading List Source URL: www.dvssel.gov.my Language: English - Date: 2014-04-13 22:18:45
630	PRESS RELEASE: Indoco receives ANDA approval for Glimepiride tablets from USFDA April 18, 2013, Mumbai: Indoco Remedies Ltd., a fast growing pharma company with a global presence, has received the USFDA approval for its Add to Reading List Source URL: www.indoco.com Language: English - Date: 2013-04-19 05:00:37 Pharmacy Clinical pharmacology Food and Drug Administration Therapeutics United States Public Health Service Abbreviated New Drug Application Glimepiride Pharmaceutical industry Pharmaceutical sciences Pharmacology Clinical research

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