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Thu, 26 Nov 2015 20:12:15 GMT狠狠撸Share feed for 狠狠撸shows by User: tarunjogiGood manufacturing practices
/slideshow/good-manufacturing-practices-55558300/55558300
goodmanufacturingpractices-151126201215-lva1-app6891 Quality of drugs is basically responsibility of manufacturers & GMP guidelines are a means to assure very quality.
Draft of GMP regulations was prepared in 1975 which could be finalized & implemented in 1988, in form of amended schedule M.
It embraces Rule 71,74,76 & 78 under D & C Rules 1945.
To achieve objectives of GMP, licensee shall comply with requirements of GMP as laid down in Schedule M.
Part I deals with GMP relating to factory premises, & Part II deals with plant & equipment for manufacture of drugs.
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Quality of drugs is basically responsibility of manufacturers & GMP guidelines are a means to assure very quality.
Draft of GMP regulations was prepared in 1975 which could be finalized & implemented in 1988, in form of amended schedule M.
It embraces Rule 71,74,76 & 78 under D & C Rules 1945.
To achieve objectives of GMP, licensee shall comply with requirements of GMP as laid down in Schedule M.
Part I deals with GMP relating to factory premises, & Part II deals with plant & equipment for manufacture of drugs.
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Thu, 26 Nov 2015 20:12:15 GMT/slideshow/good-manufacturing-practices-55558300/55558300tarunjogi@slideshare.net(tarunjogi)Good manufacturing practicestarunjogiQuality of drugs is basically responsibility of manufacturers & GMP guidelines are a means to assure very quality.
Draft of GMP regulations was prepared in 1975 which could be finalized & implemented in 1988, in form of amended schedule M.
It embraces Rule 71,74,76 & 78 under D & C Rules 1945.
To achieve objectives of GMP, licensee shall comply with requirements of GMP as laid down in Schedule M.
Part I deals with GMP relating to factory premises, & Part II deals with plant & equipment for manufacture of drugs.
<img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/goodmanufacturingpractices-151126201215-lva1-app6891-thumbnail.jpg?width=120&height=120&fit=bounds" /><br> Quality of drugs is basically responsibility of manufacturers & GMP guidelines are a means to assure very quality.
Draft of GMP regulations was prepared in 1975 which could be finalized & implemented in 1988, in form of amended schedule M.
It embraces Rule 71,74,76 & 78 under D & C Rules 1945.
To achieve objectives of GMP, licensee shall comply with requirements of GMP as laid down in Schedule M.
Part I deals with GMP relating to factory premises, & Part II deals with plant & equipment for manufacture of drugs.
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10486https://cdn.slidesharecdn.com/ss_thumbnails/goodmanufacturingpractices-151126201215-lva1-app6891-thumbnail.jpg?width=120&height=120&fit=boundspresentationBlackhttp://activitystrea.ms/schema/1.0/posthttp://activitystrea.ms/schema/1.0/posted0Antimalarial drugs
/slideshow/antimalarial-drugs-55558011/55558011
antimalarialdrugs-151126195832-lva1-app6891 anti malerials:
Metabolites of primaquine are believed to act as oxidants that are
responsible for the schizonticidal action as well as for the hemolysis
and methemoglobinemia encountered as toxicities.
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anti malerials:
Metabolites of primaquine are believed to act as oxidants that are
responsible for the schizonticidal action as well as for the hemolysis
and methemoglobinemia encountered as toxicities.
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Thu, 26 Nov 2015 19:58:32 GMT/slideshow/antimalarial-drugs-55558011/55558011tarunjogi@slideshare.net(tarunjogi)Antimalarial drugstarunjogianti malerials:
Metabolites of primaquine are believed to act as oxidants that are
responsible for the schizonticidal action as well as for the hemolysis
and methemoglobinemia encountered as toxicities.
<img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/antimalarialdrugs-151126195832-lva1-app6891-thumbnail.jpg?width=120&height=120&fit=bounds" /><br> anti malerials:
Metabolites of primaquine are believed to act as oxidants that are
responsible for the schizonticidal action as well as for the hemolysis
and methemoglobinemia encountered as toxicities.