Pharmaceutical degradation - PowerPoint PPT Presentation


Pharmaceutical-Contract-Development-and-Manufacturing-Market

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

1 views • 4 slides


Change Control in Pharmaceutical Industry

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

2 views • 14 slides



Pharmaceutical Processing Equipment Market

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

1 views • 2 slides


Understanding Physiological Acid-Base Balance in Pharmaceutical Inorganic Chemistry

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

9 views • 14 slides


Understanding Pharmaceutical Calculations and Laboratory Apparatus

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

4 views • 20 slides


Understanding Pharmaceutical Calculations: Altering Product Strength and Solutions

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

7 views • 23 slides


CPGP Study Guide and How to Crack Exam on Pharmaceutical GMP Professional

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

3 views • 35 slides


The Strategic Advantage of Pharmaceutical Staffing Agencies

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

0 views • 5 slides


ASQ Pharmaceutical GMP Professional (CPGP) Exam | Boost Your Score

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

0 views • 20 slides


Understanding Pharmaceutical Degradation: Types and Factors

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

1 views • 50 slides


Understanding Size Separation in Pharmaceutical Processing

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

1 views • 31 slides


Understanding Pharmaceutical Powders in Dosage Forms

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

2 views • 48 slides


Understanding Errors in Pharmaceutical Analysis

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

1 views • 37 slides


10 Signs It’s Time to Partner with a Pharmaceutical Staffing Agencies

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

0 views • 6 slides


Understanding Polymer Degradation Processes in Chemistry

Polymer degradation involves a reduction in molecular weight due to various factors like heating, mechanical stresses, radiation, oxygen, and moisture. Two main types of degradation include chain end degradation and random degradation, each affecting the polymer structure differently. Chain end degr

0 views • 12 slides


Understanding Fluorescence Analysis in Pharmaceutical Sciences

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

2 views • 26 slides


Pharmaceutical Quality Assurance: Unit V - Warehousing Practices by Dr. Nisha Sharma

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

1 views • 17 slides


Pharmaceutical Equipment Selection and Maintenance Guidelines for Quality Assurance

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

1 views • 20 slides


Understanding Thermogravimetric Analysis (TGA) in Pharmaceutical Applications

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

0 views • 27 slides


Principles of Calibration, Validation, and Warehousing in Pharmaceutical Quality Assurance

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

1 views • 37 slides


Sodium Benzoate: Properties, Applications, and Pharmaceutical Uses

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

0 views • 9 slides


Pharmaceutical Tablet Testing Procedures and Considerations

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

0 views • 15 slides


Inorganic Pharmaceutical Chemistry: Applications and Importance

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

1 views • 6 slides


Quality Control Tests for Pharmaceutical Packaging Materials

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

3 views • 18 slides


Overview of Pharmaceutical Packaging: Basic Terminologies, Quality Control Tests, and Container Types

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

0 views • 35 slides


Understanding Pharmaceutical Preparations: Strength and Concentration

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

0 views • 34 slides


Understanding Differential Thermal Analysis (DTA) in Pharmaceutical Applications

Differential Thermal Analysis (DTA) is a technique used in pharmaceutical applications to monitor temperature differences between a sample and reference material. By analyzing temperature changes over time or against temperature, DTA helps in detecting phase transitions and reaction temperatures in

0 views • 22 slides


Quality Control Tests for Containers, Rubber Closures, and Packaging Materials in Pharmaceutical Industry

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

1 views • 34 slides


Excessive Pricing in Pharmaceutical Markets: The Italian Experience

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

4 views • 22 slides


Enhancing Land Degradation Neutrality Targets in Lebanon's National Action Programme

Integrating LDN targets into Lebanon's National Action Programme, led by Dr. Chadi Mohanna, aims to align the NAP with the UNCCD's 10-Year Strategy, set national targets for Land Degradation Neutrality, and implement measures to combat land degradation aggravated by climate change. The project focus

0 views • 23 slides


India's Significant Contributions to Global Healthcare Through Pharmaceutical Exports

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

7 views • 7 slides


Simulation Assumptions and Performance Degradation Study on Beam Squint in 3GPP Meeting

Background on beam squint in conducted power of transmitted CCs causing radiative domain impairment and gain droop, with a problem statement on degradation of CC2 spherical coverage when CC1 and CC2 are separated by frequency. The study involves refined simulation assumptions to quantify radiative d

0 views • 7 slides


Understanding Pharmaceutical Suspensions: Types, Preparation, and Characteristics

Explore the world of pharmaceutical suspensions, including their types based on dosage form and particle size, advantages of using suspensions, features desired in pharmaceutical suspensions, and classification based on the nature of solids involved in the suspension. Learn about the preparation met

0 views • 12 slides


Addressing Land Degradation Challenges in Agriculture for Sustainable Development

World agriculture has evolved over the decades, facing challenges like environmental degradation and land misuse. Awareness-raising activities on biosafety and biodiversity are crucial for informed decision-making in agriculture. Nigeria, with its diverse ecological zones, must sustainably manage na

0 views • 13 slides


5 Steps Questionnaire on Mapping Land Degradation and Sustainable Land Management

Preparation for mapping land degradation and sustainable land management involves steps such as preparing the base map, identifying contributing specialists, assessing land use systems, understanding land degradation types, and providing expert recommendations. The process includes analyzing area tr

0 views • 32 slides


Quality Issues in Clinical Trial Materials: CMC Review by Dr. Dorota Matecka

Clinical trial materials undergo Chemistry, Manufacturing, and Controls (CMC) review to ensure pharmaceutical quality. This process includes assessing safety concerns, impurities, and specifications, along with other CMC considerations. Pharmaceutical quality encompasses the suitability, identity, s

0 views • 41 slides


Pharmaceutical Calculation and Compounding Course Overview

This course provides pharmacy students with a foundation in pharmaceutical calculations including concentration expressions, density, isotonicity, and more. The curriculum focuses on practical skills essential for pharmacy practice. Students will learn how to handle medicinal prescriptions and perfo

0 views • 46 slides


Understanding Buffers in Pharmaceutical Formulations

Buffers in pharmacy play a critical role in maintaining constant pH levels essential for drug stability and efficacy. They resist pH changes by neutralizing added acids or bases, ensuring proper drug delivery and patient comfort. Common buffer systems, such as acetic acid/sodium acetate and boric ac

4 views • 18 slides


Performance Degradation Summary for FRIB Cryomodule VT vs. Bunker

FRIB's performance degradation analysis focuses on validating the design of the cryomodule, with tests conducted under various operational conditions to assess parameters such as cryogenic losses, SRF subsystems performance, and cavity dynamics. The ReA6-1 cavity's performance, measured in terms of

0 views • 5 slides


Update on Pharmaceutical Manufacturing Plan for Africa by Dr. Djoudalbaye Benjamin

The update on pharmaceutical manufacturing plan for Africa discusses the TRIPS agreement, the inception of the Pharmaceutical Manufacturing Plan for Africa (PMPA), and the importance of promoting access to quality healthcare through local pharmaceutical manufacturing in Africa.

0 views • 25 slides