This article explains about the difference between manufacture in bond and outside bond under the Medicinal and Toilet Preparation Act 1955 with legal requirements. Manufacture In Bond Definition: Manufacturing medicinal preparations under a bond, primarily for export purposes. Key Features: Bonded Premises: Facilities authorized to produce goods for export without immediate payment of duties or … Read more
Below we have described key definitions under Medicinal and Toilet Preparation Act 1955 to understand terms related to alcohol-based drugs and cosmetics. Key terms as definitions under Medicinal and Toilet Preparation Act 1955: Medicinal Preparation: Any article intended to be used for the diagnosis, treatment, mitigation, or prevention of disease in humans or animals, including … Read more
This article explains about licenses under Medicinal and Toilet Preparation Act 1955 including types of procedures and requirements for alcohol-based products. Licensing is a critical component of the Act, ensuring that only authorized entities can manufacture, distribute, or sell medicinal and toilet preparations. Types of Licenses Under Medicinal and Toilet Preparation Act 1955: Manufacturing License: … Read more
Below we have described the objectives of Medicinal and Toilet Preparation Act 1955 aimed at regulating alcohol-based medicinal and cosmetic preparations in India. Objectives of Medicinal and Toilet Preparation Act-1955 The Medicinal and Toilet Preparations Act, 1955 was established to regulate the manufacture, sale, and distribution of medicinal and toilet preparations in India. Its primary … Read more
The solubility profile helps determine how a drug dissolves in bodily fluids, influencing its absorption and bioavailability. pKa, pH, and Log P are key parameters that affect a compound’s solubility profile and its formulation. pKa (Ionization Constant): Definition: The pH at which 50 Importance: Ionized drugs are more soluble in water, while unionized drugs have … Read more
The purity of the precipitate is essential in gravimetric analysis, as impurities can significantly affect the accuracy of results. Two common sources of impurities are co-precipitation and post-precipitation: 1. Co-precipitation: Co-precipitation occurs when impurities or other ions in the solution precipitate along with the target analyte during the precipitation process. This can happen due to: Surface … Read more
Estimation of Barium Sulfate (BaSO₄) by Gravimetric Analysis involves precipitating Ba²⁺ as BaSO₄, filtering, drying, and weighing the insoluble precipitate to determine barium content. Steps for Estimation of Barium Sulfate (BaSO₄) by Gravimetric Analysis: Sample Preparation: Weigh the sample containing barium ions (Ba²⁺) and dissolve in distilled water or dilute HCl. Filter the solution to … Read more
Diazotization titration, also known as diazo coupling titration, is a versatile and widely used method for the quantitative determination of primary aromatic amines. The technique is based on the reaction of aromatic amines with nitrous acid (HNO2) to form diazonium salts, which can further couple with suitable coupling agents to form highly colored azo compounds. … Read more
Gravimetric analysis of magnesium sulfate involves precipitating magnesium as magnesium ammonium phosphate and weighing the dried precipitate to determine magnesium content. Principle: Gravimetric analysis is a quantitative method that determines the amount of an analyte based on its mass. The analyte is isolated, typically as a precipitate, which is then weighed to calculate the analyte’s … Read more
Offences and Penalties Under the Pharmacy Act 1948 The Pharmacy Act, 1948, outlines various offences and corresponding penalties to ensure adherence to professional standards and legal requirements. Common Offences: Practicing Without Registration: Engaging in pharmacy practice without registration. Misrepresentation: Providing false information during registration or on documents. Violation of Ethics: Unethical practices, such as accepting … Read more
