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2010 2 1722. Ali E. Qarabadeen-e-Ehsani. 2nd Edition. New Delhi CCRUM Dept. of AYUSH Ministry of Health and Family Welfare Govt. of India 2006. 201 Jalaluddin 2006 Ali 2006 Khan 2006 Khan 2005. Table 3. Total number of dosage forms. 202 Need of modification in dosage forms Total 203 At present nearly 90 dosage forms are recorded in Numbers 204 different Unani pharmacopoeias Arzani 1998 Said Jamid Advia Solid dosage forms 205 1997 Ibn Sina 2006 Ghani 2010 Kabeeruddin 1935 Neem Jamid Advia...
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What is modification in unani drug?
Modification in unani drug refers to any change or update made to the formulation, manufacturing process, labeling, or any other aspect of the drug.
Who is required to file modification in unani drug?
The manufacturer or distributor of the unani drug is responsible for filing the modification.
How to fill out modification in unani drug?
To fill out a modification in unani drug, the manufacturer or distributor must provide details of the proposed changes and submit them to the relevant regulatory authority.
What is the purpose of modification in unani drug?
The purpose of modification in unani drug is to ensure the safety, efficacy, and quality of the drug is maintained and any changes are properly documented and regulated.
What information must be reported on modification in unani drug?
The information that must be reported on modification in unani drug includes the nature of the modification, rationale for the change, impact on the drug's safety and efficacy, and any supporting data or documentation.
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