際際滷shows by User: BhanuPrasad10 / http://www.slideshare.net/images/logo.gif 際際滷shows by User: BhanuPrasad10 / Fri, 04 Mar 2016 10:48:54 GMT 際際滷Share feed for 際際滷shows by User: BhanuPrasad10 Impurities in drug substance (ich q3 a) /slideshow/impurities-in-drug-substance-ich-q3-a/59065696 impuritiesindrugsubstanceichq3a-160304104854
Impurities in drug substance]]>

Impurities in drug substance]]>
Fri, 04 Mar 2016 10:48:54 GMT /slideshow/impurities-in-drug-substance-ich-q3-a/59065696 BhanuPrasad10@slideshare.net(BhanuPrasad10) Impurities in drug substance (ich q3 a) BhanuPrasad10 Impurities in drug substance <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/impuritiesindrugsubstanceichq3a-160304104854-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Impurities in drug substance
Impurities in drug substance (ich q3 a) from Bhanu Chava
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US DMF Preparation and submission /slideshow/us-dmf-preparation-and-submission/43851667 usdmfpreparationandsubmission-150124054728-conversion-gate02
Drug Master File Preparation and submission to US FDA]]>

Drug Master File Preparation and submission to US FDA]]>
Sat, 24 Jan 2015 05:47:27 GMT /slideshow/us-dmf-preparation-and-submission/43851667 BhanuPrasad10@slideshare.net(BhanuPrasad10) US DMF Preparation and submission BhanuPrasad10 Drug Master File Preparation and submission to US FDA <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/usdmfpreparationandsubmission-150124054728-conversion-gate02-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Drug Master File Preparation and submission to US FDA
US DMF Preparation and submission from Bhanu Chava
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21 cfr part 210 and 211 /slideshow/21-cfr-part-210-and-211/42866950 21cfrpart210and211-141219060438-conversion-gate02
an overview of 21 CFR Part 210 and 210]]>

an overview of 21 CFR Part 210 and 210]]>
Fri, 19 Dec 2014 06:04:38 GMT /slideshow/21-cfr-part-210-and-211/42866950 BhanuPrasad10@slideshare.net(BhanuPrasad10) 21 cfr part 210 and 211 BhanuPrasad10 an overview of 21 CFR Part 210 and 210 <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/21cfrpart210and211-141219060438-conversion-gate02-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> an overview of 21 CFR Part 210 and 210
21 cfr part 210 and 211 from Bhanu Chava
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https://cdn.slidesharecdn.com/profile-photo-BhanuPrasad10-48x48.jpg?cb=1716959228 Experienced Deputy Manager with a demonstrated history of working in the chemicals industry. Skilled in U.S. Food and Drug Administration (FDA), Good Laboratory Practice (GLP), Validation, GMP, and Regulatory Affairs. https://cdn.slidesharecdn.com/ss_thumbnails/impuritiesindrugsubstanceichq3a-160304104854-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/impurities-in-drug-substance-ich-q3-a/59065696 Impurities in drug sub... https://cdn.slidesharecdn.com/ss_thumbnails/usdmfpreparationandsubmission-150124054728-conversion-gate02-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/us-dmf-preparation-and-submission/43851667 US DMF Preparation and... https://cdn.slidesharecdn.com/ss_thumbnails/21cfrpart210and211-141219060438-conversion-gate02-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/21-cfr-part-210-and-211/42866950 21 cfr part 210 and 211