Project Challenge: Existing formulation (lower strength - 50 mg) was manufactured using direct compression process.

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In addition, the growing demand for cell and gene therapies and personalized medicines and growth in the High-potency Active Pharmaceutical Ingredients (HPAPI) and Antibody-drug Conjugates (ADC) markets are expected to offer significant opportunities for the growth of the pharmaceutical contract dev

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Change control in the pharmaceutical industry is a critical process that ensures the management of alterations to maintain product quality and compliance with regulatory standards. It involves categorizing changes as minor, major, or critical, each requiring specific handling to minimize risks and u

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Learn about the formulation and use of nasal and ear drops in pharmaceutical technology labs. Explore details on nasal drops for nasal passages, ephedrine nasal drop recipe, notes on ingredients, ear drops for ear care, sodium bicarbonate ear drop recipe, and procedures for preparation. Understand t

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Pharmaceutical processing includes a range of unit operations such as blending, milling, granulation, tablet pressing, coating, and filling, depending on the mode of delivery. With the growing adoption of continuous manufacturing and the rising number of novel therapies in clinical development, phar

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This lecture delves into the fundamental concepts of pharmaceutical inorganic chemistry, focusing on the mechanisms and uses of various pharmaceutical products that correct body disorders. Topics covered include acids and bases, intra and extracellular electrolytes, and the role of buffers in mainta

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Pharmaceutical preparations must be effective, safe, and accurate in both quantitative and qualitative aspects. This includes ensuring the accurate amount and identity of ingredients. Laboratory apparatus such as mortar and pestle, wide mouth bottles, cylindrical and conical measure cylinders, and c

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Pharmaceutical calculations involve altering the strength of pharmaceutical preparations by adjusting the proportion of active ingredients, using stock solutions, and problem-solving techniques. This process includes dilution, fortification, and concentration changes to achieve desired product stren

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Click Here--- \/\/bit.ly\/4bsglWA ---Get complete detail on CPGP exam guide to crack Pharmaceutical GMP Professional. You can collect all information on CPGP tutorial, practice test, books, study material, exam questions, and syllabus. Firm your knowledge on Pharmaceutical GMP Professional and get r

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Unlock the strategic advantages of pharmaceutical staffing agencies. Explore how they accelerate R&D, streamline hiring, ensure compliance, and support emerging fields. Partner with us for enhanced innovation and success in the industry. For more information, visit: \/pharmaceutical-recruitment-age

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Click Here---> \/\/bit.ly\/4bsglWA <---Get complete detail on CPGP exam guide to crack Pharmaceutical GMP Professional. You can collect all information on CPGP tutorial, practice test, books, study material, exam questions, and syllabus. Firm your knowledge on Pharmaceutical GMP Professional and get

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Pharmaceutical degradation refers to the process of a formulation in a specific container losing its chemical, microbiological, therapeutic, physical, and toxicological specifications. It can be categorized into physical, chemical, and microbiological degradation. Physical degradation alters the dru

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Size separation is a crucial unit operation in pharmaceutical manufacturing, involving the segregation of particles based on physical differences like size, shape, and density. This process, also known as sieving or screening, is essential for improving powder mixing, particle solubility, and stabil

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Pharmaceutical powders play a vital role in various dosage forms, serving as carriers of active ingredients and enabling diverse administration routes. They are meticulously characterized for their physical and chemical properties before being utilized in medicinal preparations. Furthermore, the con

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This article explores different types of errors in pharmaceutical analysis, such as determinate and indeterminate errors, and discusses their impact on analysis results. It also covers the concepts of accuracy, precision, and minimizing systematic errors in analytical chemistry. The importance of id

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Pharmaceutical aerosols are pressurized systems used for delivering therapeutic active ingredients. They consist of components like propellants, containers, valves, and product concentrate. The use of aerosols offers advantages such as targeted delivery, reduced irritation, and ease of application.

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Find out the top 10 indicators that signal it's time to partner with a pharmaceutical staffing agency. Enhance your hiring process, access top talent, and stay ahead in the competitive pharmaceutical industry with expert staffing solutions. For more

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Fluorescence analysis is a crucial technique in pharmaceutical analysis, involving the emission of radiation by molecules when excited at specific wavelengths. Factors influencing fluorescence, such as concentration, light intensity, adsorption, oxygen presence, pH, temperature, viscosity, and photo

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A pharmaceutical suspension is a dispersion of finely divided insoluble material in a liquid medium, available in liquid or dry form. These suspensions are essential for unstable drugs and come in different particle sizes, from colloidal to coarse. The particles in a suspension vary in size, influen

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Explore the importance of good warehousing practices in the pharmaceutical industry as discussed in the 6th-semester course of Pharmaceutical Quality Assurance. Dr. Nisha Sharma elaborates on the concepts of warehousing, GWP, key activities, functions, and elements of good warehousing practices, emp

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This content focuses on the selection, purchase specifications, and maintenance of equipment and raw materials in pharmaceutical quality assurance. It emphasizes the importance of well-defined selection procedures, strategic impact on business, and considerations for equipment design, size, and main

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Thermogravimetric Analysis (TGA) is a technique that measures weight changes in a material as it is heated or cooled. This analysis helps in understanding decomposition, stability, and purity of pharmaceutical compounds. TGA operates on the principle of monitoring mass changes with temperature, offe

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Calibration and validation are critical processes in maintaining the quality of pharmaceutical products. Validation ensures that processes result in expected outcomes consistently, meeting quality standards. Qualification is an essential part of validation, ensuring that equipment and systems perfor

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Sodium benzoate is a white crystalline powder with various physical and chemical properties. It is commonly used as a preservative in pharmaceutical formulations, cough preparations, and cosmetic products. Additionally, it has pharmaceutical applications in treating urea cycle disorders and schizoph

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This informative content delves into weight variation, content uniformity, and disintegration tests conducted in pharmaceutical laboratories. It discusses official testing methods, factors affecting test outcomes, and requirements for ensuring potency uniformity and tablet quality. Content covers we

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Inorganic pharmaceutical chemistry explores the study of elements and compounds excluding carbon, with diverse applications in pharmacy. It encompasses the synthesis and use of inorganic compounds in drug development, catalysis, pigments, and agriculture. The field also delves into the medicinal val

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This article discusses quality control tests for pharmaceutical packaging materials focusing on glass containers. The tests include chemical resistant tests such as powdered glass test and water attack test, as well as hydrolytic resistance tests. Detailed procedures for each test are outlined along

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Pharmaceutical packaging plays a crucial role in maintaining the effectiveness and safety of medications. This content delves into basic terminologies, quality control tests for containers, closures, and secondary packaging, as well as an introduction to general packaging practices. It also covers t

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Pharmaceutical preparations can have their strength and concentration adjusted by changing the proportion of active ingredients. This process involves increasing or decreasing the active ingredient, adding diluents, admixing with other preparations, or evaporating the vehicle. Dilution of liquid, so

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Quality control testing is essential for containers, rubber closures, and secondary packaging materials in the pharmaceutical industry to ensure product protection, identification, and presentation. Various materials like glass, plastic, metal, and rubber are used for containers and closures, each h

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Understanding the formulation and design of dosage forms is crucial in pharmaceutical sciences. Drug substances are combined with nonmedicinal agents to create stable, effective, and safe products. Considerations such as compatibility, quality control, labeling, and storage play key roles in dosage

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Pharmaceutical incompatibilities can lead to issues during compounding, dispensing, or administration of drugs. They are classified into physical, chemical, and therapeutic types, with potential delays or reduction in therapeutic effectiveness. Physical incompatibilities may involve insolubility or

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Understanding pH-solubility profiles of drugs like indomethacin, chlorpromazine, and oxytetracycline is crucial in formulating pharmaceuticals. Factors affecting dissolution rates, such as particle size and solubility, can be optimized to enhance drug absorption. Different methods like particle size

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The presentation by Andrea Pezzoli explores the issue of excessive pricing in pharmaceutical markets, focusing on the Italian experience. It covers cases of infringement on excessive prices, such as the Aspen pharmaceutical group's fine for unfair pricing. The regulatory framework in Italy, includin

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Pharmaceutical suspensions are dispersions of insoluble solid particles in a fluid medium, commonly aqueous. They offer benefits like increased drug stability, improved palatability, and ease of administration. Formulation considerations include homogeneity, re-suspension ability, particle size, and

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India, a key player in the global pharmaceutical sector, significantly contributes to global health through its pharmaceutical exports. The country provides generic medicines to over 200 countries, with a notable presence in highly regulated markets. India's pharmaceutical exports showcase impressiv

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Understanding the definition of medicinal products, drug actions, and formulation development processes is crucial for efficient medicine administration. Proper adherence to medication rights ensures safe and effective treatment delivery, emphasizing the importance of dosage form development through

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Bordoloi Biotech India Pvt Ltd presents HerboJoint, a unique natural formulation designed to provide freedom from joint pain. Developed by a team of experts led by Dr. Binoy B. Bordoloi and Dr. Kulwant S. Saini, HerboJoint is a scientifically backed product combining essential oils with proven effic

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This chapter on interior point methods in convex optimization explores the formulation of inequality-constrained optimization problems using barrier methods and generalized inequalities. It covers primal-dual interior point methods and discusses issues such as exponential complexity and determining

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Exploring the formulation and modeling of spring-mass systems as Cauchy problems, focusing on the basics of Hooke's Law and Newton's Second Law of Motion. Dive into the analysis of systems with multiple masses and springs, examining the ODEs that describe their motion and the formulation of solution

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