SCHEDULE M – GMP – PART 6 (METERED-DOSE-INHALERS)
GOOD MANUFACTURING PRACTICES FOR METERED-DOSE-INHALERS (MDI)
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SCHEDULE M – GMP – PART 5 (TOPICAL PRODUCTS)
GOOD MANUFACTURING PRACTICES FOR TOPICAL PRODUCTS i.e. EXTERNAL PREPARATIONS (CREAMS, OINTMENTS, PASTES, MULSIONS, LOTIONS, SOLUTIONS, DUSTING POWDERS AND IDENTICAL PRODUCTS)
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SCHEDULE M – GMP – PART 4 (ORAL LIQUIDS)
GOOD MANUFACTURING PRACTICES FOR ORAL LIQUIDS (SYRUPS, ELIXIRS, EMULSIONS AND SUSPENSIONS)
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STANDARD SOLUTIONS FOR LIMIT TESTS
Standard Solutions For Limit Tests Preparation | Limit Tests Solutions Preparation |
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SCHEDULE M – GMP – PART 3 (PARENTERAL PREPARATIONS)
GOOD MANUFACTURING PRACTICES FOR STERILE PRODUCTS, PARENTERAL PREPARATIONS (SMALL VOLUME INJECTABLES AND LARGE VOLUME PARENTERALS) AND STERILE OPHTHALMIC PREPARATIONS.
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SCHEDULE M – GMP – PART 2 (OSD)
GOOD MANUFACTURING PRACTICES FOR ORAL SOLID DOSAGE FORMS (TABLETS AND CAPSULES)
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Data Integrity – ALCOA+
Data integrity is the fundamental principle of ensuring that data is accurate, reliable, and consistent throughout its entire lifecycle.
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What is CAPA – Corrective and preventative action
Corrective and preventative action (CAPA) in pharma refers to the process of identifying, investigating, and addressing any issues or deviations that may have occurred during the production of pharmaceutical products.
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Bursting Strength Tester
General information on Bursting Strength Tester
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SOP for Bursting Strength Tester
SOP for Bursting Strength Tester | SOP for Cleaning and Operation of Bursting Strength Tester |
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