GMP AND QC OF CHURNAS - amam-ayurveda.org

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GMP and QC of Churna Contd. The no of ingredients are large, same can be listed in a leaflet and can be kept inside the packet and reference should be made on the level. Official names of the drug as mentioned in AFI should be given. Apart from this, Manufacturing license, date of manufacture, batch no, exp date, shall also be mentioned.
GMP and QC of Churna Contd. If any ingredients belongs to the Schedule-E- 1, should be leveled with “caution”, to be taken under medical supervision. For export purpose, the label should contain information's as per the directives of the importing country.
Page 1 and 2: GOOD MANUFACTURING PRACTICES(GMP) A
Page 3 and 4: GMP and QC of Churna Contd. Definit
Page 5 and 6: GMP and QC of Churna Contd. General
Page 7 and 8: GMP and QC of Churna Contd. Workers
Page 9 and 10: GMP and QC of Churna Contd. Premanu
Page 11 and 12: GMP and QC of Churna Contd. Process
Page 13 and 14: GMP and QC of Churna Contd. Mass mi
Page 15 and 16: GMP and QC of Churna Contd. Asa foe
Page 17 and 18: GMP and QC of Churna Contd. Packagi
Page 19: GMP and QC of Churna Contd. Labelin
Page 23 and 24: GMP and QC of Churna Contd. Quality
Page 25 and 26: GMP and QC of Churna Contd. Loss on
Page 27: THANK YOU ALL

GMP AND QC OF CHURNAS - amam-ayurveda.org

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