Capsules are solid dosage forms that contain a drug or mixture of drugs enclosed within a shell. The shell is typically made of gelatin but can also be other materials. Capsules are intended for oral administration and provide rapid release of contents unless they are modified or enteric release capsules. Capsules can be filled using various methods like auger, dosator, or dosing disc systems. Tests are conducted to ensure uniformity of contents, weight, and dissolution based on pharmacopeial standards.
This document provides information about the Ayurvedic procedure of kshetrikaranam (body purification) prior to initiating medical therapies. It discusses the etymology and definition of kshetrikaranam. The key steps of kshetrikaranam include pachanam, snehanam, vamanam, virechanam and krimipaatanam. Specific techniques and durations are mentioned for each step. The purpose of kshetrikaranam is to properly cleanse and prepare the body to maximize the effects of subsequent medical treatments.
This document provides definitions and evaluation methods for solid oral dosage forms like tablets and capsules. It defines tablets as containing an active ingredient with or without excipients prepared by molding or compression, and capsules as containing the active ingredient filled into a cap and body. It describes methods like disintegration testing using baskets, dissolution testing using paddle or basket apparatuses, content uniformity testing, weight variation testing, friability testing, and moisture permeation testing to evaluate important properties of tablets and capsules.
This document discusses evaluation parameters for tablets, including non-official and official tests. It provides details on tablet size, shape, color, markings and organoleptic properties. Official tests covered include weight variation, hardness, friability, disintegration and dissolution. Weight variation ensures uniform tablet weights. Hardness and friability test tablet strength and stability. Disintegration and dissolution tests simulate how tablets break down in the body. Content uniformity also evaluates active ingredient amounts in tablets.
This document provides information about Pratisarana (application of medicine inside the mouth) and discusses different types used for this including Kalka (paste), Avaleha (linctus), and Churna (powder). It also summarizes the ingredients and uses of toothpaste, tooth powder, and mouthwash for oral healthcare.
Capsules are solid dosage forms that contain a drug or mixture of drugs enclosed within a shell. The shell is typically made of gelatin but can also be other materials. Capsules are intended for oral administration and provide rapid release of contents unless they are modified or enteric release capsules. Capsules can be filled using various methods like auger, dosator, or dosing disc systems. Tests are conducted to ensure uniformity of contents, weight, and dissolution based on pharmacopeial standards.
This document provides information about the Ayurvedic procedure of kshetrikaranam (body purification) prior to initiating medical therapies. It discusses the etymology and definition of kshetrikaranam. The key steps of kshetrikaranam include pachanam, snehanam, vamanam, virechanam and krimipaatanam. Specific techniques and durations are mentioned for each step. The purpose of kshetrikaranam is to properly cleanse and prepare the body to maximize the effects of subsequent medical treatments.
This document provides definitions and evaluation methods for solid oral dosage forms like tablets and capsules. It defines tablets as containing an active ingredient with or without excipients prepared by molding or compression, and capsules as containing the active ingredient filled into a cap and body. It describes methods like disintegration testing using baskets, dissolution testing using paddle or basket apparatuses, content uniformity testing, weight variation testing, friability testing, and moisture permeation testing to evaluate important properties of tablets and capsules.
This document discusses evaluation parameters for tablets, including non-official and official tests. It provides details on tablet size, shape, color, markings and organoleptic properties. Official tests covered include weight variation, hardness, friability, disintegration and dissolution. Weight variation ensures uniform tablet weights. Hardness and friability test tablet strength and stability. Disintegration and dissolution tests simulate how tablets break down in the body. Content uniformity also evaluates active ingredient amounts in tablets.
This document provides information about Pratisarana (application of medicine inside the mouth) and discusses different types used for this including Kalka (paste), Avaleha (linctus), and Churna (powder). It also summarizes the ingredients and uses of toothpaste, tooth powder, and mouthwash for oral healthcare.
This document discusses the process of satvapatana, which is the extraction of the active principle or essence from minerals and metals. It begins by defining satvapatana and classifying it based on the form of satva extracted, the nature of the material, and the satva obtained. The document then outlines the aims, methods, equipment, and materials used in satvapatana like crucibles, fluxes, and heat sources. Specific extraction processes are provided for minerals like manahshila and metals. Analysis of the extracted satva is also presented. The conclusion differentiates satvapatana from metallurgy and emphasizes its therapeutic goal of obtaining an active principle.
Pharmaceutical dosage forms and drug delivery systemsVIJAY SINGH
This document provides an overview of basic information on pharmaceutical dosage forms and drug delivery systems. It discusses active drug substances and the need for dosage forms to deliver drugs effectively. Common dosage forms are described for oral, rectal, and other systemic routes of administration. These include tablets, capsules, liquids, and suppositories. Immediate and controlled release solid oral dosage forms are also covered. The document aims to familiarize readers with common dosage forms and factors influencing drug delivery through different systems.
This presentation discusses pharmaceutical tablets. It introduces tablets as a solid dosage form that can contain one or more medicaments with or without excipients, prepared by molding or compression. The presentation describes different types of tablets including plain, chewable, buccal, sublingual, and enteric coated tablets. It outlines the advantages of tablets being easy to administer, stable, and able to accurately deliver medication, as well as disadvantages like unsuitability for unconscious patients.
The document discusses guidelines for standardization and quality control of herbal drugs and formulations. It describes various parameters for standardization including macroscopic, microscopic, physical, chemical and biological evaluations. Specific tests covered include determination of foreign matter, ash values, extractive values, water soluble ash, total solid content, water content, volatile oil content, bitterness value, haemolytic activity, tannin content, swelling index and foaming index. Standardization helps in confirmation of identity, quality and purity of herbal drugs.
Kupipakwa Rasayan by Mohd Ehsan B.Pharm (Ayurveda) StudentMohd Ehsan
The document discusses Kupipakwa rasayan, a unique Ayurvedic preparation. It begins by providing historical context for the development of rasashastra as a branch of Ayurveda. It then defines key terms like kajjali, jarana, and murcchana used in the Kupipakwa process. The document outlines the typical materials, steps, and observations involved in the preparation method. These include using a kupi vessel placed in a valuka yantra and applying different levels of heat. The summary concludes that Kupipakwa rasayan formulations are effective treatments due to the high heat applied making drugs easily absorbable.
The document lists over 40 postgraduate programs, diplomas, fellowships, and certificate courses that are available career options after completing a BAMS degree in Ayurveda, including options for further specialization in various medical fields like cardiology, nutrition, public health, and rehabilitation as well as some business-related options. It also provides brief descriptions of the requirements and job opportunities for some of these career paths, including working as a lecturer, scientist, sales representative, or starting a private practice.
Dosage forms (also called unit doses) are pharmaceutical drug products in the form in which they are marketed for use, with a specific mixture of active ingredients and inactive components (excipients), in a particular configuration (such as a capsule shell, for example), and apportioned into a particular dose. For example, two products may both be amoxicillin, but one is in 500 mg capsules and another is in 250 mg chewable tablets. The term unit dose can also sometimes encompass non-reusable packaging as well (especially when each drug product is individually packaged[1]), although the FDA distinguishes that by unit-dose "packaging" or "dispensing".[2] Depending on the context, multi(ple) unit dose can refer to distinct drug products packaged together, or to a single drug product containing multiple drugs and/or doses. The term dosage form can also sometimes refer only to the pharmaceutical formulation of a drug product's constituent drug substance(s) and any blends involved, without considering matters beyond that (like how it is ultimately configured as a consumable product such as a capsule, patch, etc.). Because of the somewhat vague boundaries and unclear overlap of these terms and certain variants and qualifiers thereof within the pharmaceutical industry, caution is often advisable when conversing with someone who may be unfamiliar with another person's use of the term.
Depending on the method/route of administration, dosage forms come in several types. These include many kinds of liquid, solid, and semisolid dosage forms. Common dosage forms include pill, tablet, or capsule, drink or syrup, and natural or herbal form such as plant or food of sorts, among many others. Notably, the route of administration (ROA) for drug delivery is dependent on the dosage form of the substance in question. A liquid dosage form is the liquid form of a dose of a chemical compound used as a drug or medication intended for administration or consumption.
Various dosage forms may exist for a single particular drug, since different medical conditions can warrant different routes of administration. For example, persistent nausea, especially with vomiting, may make it difficult to use an oral dosage form, and in such a case, it may be necessary to use an alternative route such as inhalational, buccal, sublingual, nasal, suppository or parenteral instead. Additionally, a specific dosage form may be a requirement for certain kinds of drugs, as there may be issues with various factors like chemical stability or pharmacokinetics. As an example, insulin cannot be given orally because upon being administered in this manner, it is extensively metabolized in the gastrointestinal tract (GIT) before reaching the blood stream, and is thereby incapable of sufficiently reaching its therapeutic target destinations. The oral and intravenous doses of a drug such as paracetamol will differ for the same reason
Analysis of parenteral dosage forms bjl final seminarPatel Parth
This document provides an overview of analytical testing for parenteral formulations. It discusses the need for quality assurance in parenterals due to risks of improper administration. The main types of parenterals are classified and key characteristics like sterility are outlined. Analytical methods for raw materials, finished products, and stability studies are summarized, including identification, potency, degradation products, pH and particulate testing. Microbiological tests like sterility and bacterial endotoxins are also covered at a high level.
'Rasasastra' ,is the science of metals , minerals , other toxic herbs , which are applied for attaining two goals. It is either used in the perspective of metallurgy, where lower metals are converted in to higher metals. It is otherwise used for the attainment of supreme health. This science , with both the applications were once well practiced in our country. But due to several factors, this divine science has been restricted to treatment aspect. 'Kshetreekarana' is the method of preparing the body to be eligible for administering processed divine mercury. In the midst various references Kshetreekarana generally , includes two steps. The first step is implementing Panchakarma therapy and second step involves administration of special formulations to attain a healthy condition to accept the divine mercury.
This document provides an overview of tablets as a pharmaceutical dosage form. It discusses the historical development of tablets, advantages and disadvantages, ideal tablet properties, and methods for evaluating tablets. Key aspects covered include tablet composition, compression, granulation, design and formulation. Evaluation methods summarized are general appearance, size and shape, identification markings, organoleptic properties, hardness and friability, drug content and release, weight uniformity, disintegration, and dissolution testing. The compression operation and basic components of tablet presses are also outlined.
This document discusses tablets as a dosage form for delivering medications. It defines tablets and outlines their advantages such as precise dosing, low cost, and stability. Various types of tablets are described based on where they are administered and how they release the drug. The key ingredients used in tablets called excipients are explained. Granulation techniques for tablet manufacturing like wet and dry granulation are summarized. The document also covers tablet processing problems that can occur and ways to control the manufacturing process.
Ayurveda strongly believes in using drugs with particular tastes in treating diseases. This presentation will help you understand the basics of rasa and its applied aspects in planning treatment protocol.
compilation of the inormation about Shilajeet/ salajeet from texts and internet. contents
classical references,
purification of Shilajeet,
medicinal uses of shilajeet,
Side effects of Shilajeet,
dose of Shilajeet,
aphrodisiac and other effects of Shilajeet
health benefits of shilajeet
chemical constituents of Shilajeet
Concept of Agni in Rasa Shastra & BhaishajyaNitika Rattan
Agni plays a key role in Ayurveda and Rasa Shastra. There are different types of Agni in the body and processes like Bhasmikaran use Agni to convert metals and minerals into microfine forms. Putas are methods of heating that are classified based on the level of heat intensity. Putas are an important part of the Marana process and influence the properties of the final Bhasma. Electric furnaces can now also be used as a controlled source of heat for Rasa Shastra procedures like Bhasmikaran.
Tablets are solid dosage forms made by compressing or molding mixtures of active and inactive ingredients. They are the most popular dosage form due to their accurate dosing, low cost, stability and ease of production. Tablets can be formulated for immediate or controlled release and come in various shapes, sizes and coatings. The manufacturing process involves mixing and granulating powders, then compressing them into tablets using either wet or dry granulation methods. Wet granulation is more common and involves using a liquid binder to form granules which are then dried, sized, lubricated and compressed. Tablets must balance physical attributes like strength with chemical properties like drug release.
The document provides details on quality control tests conducted on tablets, including physical tests like hardness, thickness, friability, and chemical tests like content uniformity and dissolution. It describes the purpose, equipment, and procedures for tests like hardness, thickness and diameter, friability, disintegration, weight variation, content uniformity, assay, and dissolution. The tests are essential to ensure tablets meet specifications for attributes like strength, thickness, ability to withstand abrasion, breakdown time, uniform drug content, and drug release rate.
tamra ppt new..pptx rasa shastra and bhaisajya kalpanarakhan78619
This document provides information about copper (tamra) including its Sanskrit and English names, chemical formula, properties, synonyms, geographical distribution, types, purification process, and methods of preparation as a bhasma for medicinal use according to classical Ayurvedic texts. Key points include that copper has high thermal and electrical conductivity, two types are distinguished based on source (Naipalika and Mleccha), and purification involves heating and dipping in specified liquids while preparation as a bhasma involves intricate multi-step processes including trituration and enclosure in pots for heating. The bhasma must then undergo an amritikarana process to remove toxicity before medicinal use.
Hard gelatin capsules are solid dosage forms where medicaments are enclosed in gelatin shells composed of two sections called caps and bodies. Capsules offer advantages like easy swallowing, taste masking, and protection from light. They are manufactured by dipping stainless steel pins in gelatin solution, spinning to distribute gelatin uniformly, drying, stripping caps and bodies, trimming, and joining. Capsules are filled using machines that separate caps from bodies, fill powder into bodies using various techniques like auger filling or piston tamping, scrape excess powder, replace caps, and seal capsules. Finished capsules are evaluated for tests like disintegration, dissolution, content uniformity and weight variation.
Quality Control Tests For Tablets and Capsules(QC)mdpavel
This document discusses quality control tests for tablets and capsules. It describes tests for general appearance, size, shape, thickness, color, and odor. It then compares quality control tests from the British, Indian, and United States Pharmacopoeias, including tests for content of active ingredients, disintegration, uniformity of content and weight, and labeling. Specific tests are described for different types of tablets, including uncoated, enteric coated, dispersible, and modified release tablets. Common non-official tests like hardness and friability are also summarized.
Santosh Kumar Tripathy is a DCDP currently working at Madinat Jumeirah in Dubai since 2016. He has over 10 years of experience in roles such as DCDP, Commis I, II, and III at hotels in Dubai, Ras Al Khaimah, Mumbai, and Hyderabad. He holds a diploma in F&B production from the Institute of Hotel Management in Bhubaneswar, India. His objective is to pursue a challenging career utilizing his education and skills to advance professionally and increase his knowledge.
אנחנו חיים בעולם מרובה ערוצים, מרובה מסכים, מרובה רשתות... המון קורה ובקצב מהיר. כולנו רוצים להיות מעודכנים בהכל עכשיו ומיד אבל בפועל אין לנו זמן... מקסימום יכולים לתפוס את ה"צינור".
בדיוק לשם כך, מחלקת מחקר אסטרטגי יצרה עבורכם את Spot‘it- סקירה שבועית שתאפשר לכם בצורה הפשוטה והקלה ביותר להתעדכן תוך מספר דקות בכל מה שחם ומעורר השראה בתרבות האינטרנט העכשווית.
ה-כול החל מסרטוני הרשת הוויראליים ביותר, פרסומות ומהלכים שיווקיים מעוררי השראה, הקליפים הנצפים ביותר, תכניות הטלוויזיה הכי מדוברות, הסרטים הכי חדשים ועוד, ועוד, ועוד...
This document discusses the process of satvapatana, which is the extraction of the active principle or essence from minerals and metals. It begins by defining satvapatana and classifying it based on the form of satva extracted, the nature of the material, and the satva obtained. The document then outlines the aims, methods, equipment, and materials used in satvapatana like crucibles, fluxes, and heat sources. Specific extraction processes are provided for minerals like manahshila and metals. Analysis of the extracted satva is also presented. The conclusion differentiates satvapatana from metallurgy and emphasizes its therapeutic goal of obtaining an active principle.
Pharmaceutical dosage forms and drug delivery systemsVIJAY SINGH
This document provides an overview of basic information on pharmaceutical dosage forms and drug delivery systems. It discusses active drug substances and the need for dosage forms to deliver drugs effectively. Common dosage forms are described for oral, rectal, and other systemic routes of administration. These include tablets, capsules, liquids, and suppositories. Immediate and controlled release solid oral dosage forms are also covered. The document aims to familiarize readers with common dosage forms and factors influencing drug delivery through different systems.
This presentation discusses pharmaceutical tablets. It introduces tablets as a solid dosage form that can contain one or more medicaments with or without excipients, prepared by molding or compression. The presentation describes different types of tablets including plain, chewable, buccal, sublingual, and enteric coated tablets. It outlines the advantages of tablets being easy to administer, stable, and able to accurately deliver medication, as well as disadvantages like unsuitability for unconscious patients.
The document discusses guidelines for standardization and quality control of herbal drugs and formulations. It describes various parameters for standardization including macroscopic, microscopic, physical, chemical and biological evaluations. Specific tests covered include determination of foreign matter, ash values, extractive values, water soluble ash, total solid content, water content, volatile oil content, bitterness value, haemolytic activity, tannin content, swelling index and foaming index. Standardization helps in confirmation of identity, quality and purity of herbal drugs.
Kupipakwa Rasayan by Mohd Ehsan B.Pharm (Ayurveda) StudentMohd Ehsan
The document discusses Kupipakwa rasayan, a unique Ayurvedic preparation. It begins by providing historical context for the development of rasashastra as a branch of Ayurveda. It then defines key terms like kajjali, jarana, and murcchana used in the Kupipakwa process. The document outlines the typical materials, steps, and observations involved in the preparation method. These include using a kupi vessel placed in a valuka yantra and applying different levels of heat. The summary concludes that Kupipakwa rasayan formulations are effective treatments due to the high heat applied making drugs easily absorbable.
The document lists over 40 postgraduate programs, diplomas, fellowships, and certificate courses that are available career options after completing a BAMS degree in Ayurveda, including options for further specialization in various medical fields like cardiology, nutrition, public health, and rehabilitation as well as some business-related options. It also provides brief descriptions of the requirements and job opportunities for some of these career paths, including working as a lecturer, scientist, sales representative, or starting a private practice.
Dosage forms (also called unit doses) are pharmaceutical drug products in the form in which they are marketed for use, with a specific mixture of active ingredients and inactive components (excipients), in a particular configuration (such as a capsule shell, for example), and apportioned into a particular dose. For example, two products may both be amoxicillin, but one is in 500 mg capsules and another is in 250 mg chewable tablets. The term unit dose can also sometimes encompass non-reusable packaging as well (especially when each drug product is individually packaged[1]), although the FDA distinguishes that by unit-dose "packaging" or "dispensing".[2] Depending on the context, multi(ple) unit dose can refer to distinct drug products packaged together, or to a single drug product containing multiple drugs and/or doses. The term dosage form can also sometimes refer only to the pharmaceutical formulation of a drug product's constituent drug substance(s) and any blends involved, without considering matters beyond that (like how it is ultimately configured as a consumable product such as a capsule, patch, etc.). Because of the somewhat vague boundaries and unclear overlap of these terms and certain variants and qualifiers thereof within the pharmaceutical industry, caution is often advisable when conversing with someone who may be unfamiliar with another person's use of the term.
Depending on the method/route of administration, dosage forms come in several types. These include many kinds of liquid, solid, and semisolid dosage forms. Common dosage forms include pill, tablet, or capsule, drink or syrup, and natural or herbal form such as plant or food of sorts, among many others. Notably, the route of administration (ROA) for drug delivery is dependent on the dosage form of the substance in question. A liquid dosage form is the liquid form of a dose of a chemical compound used as a drug or medication intended for administration or consumption.
Various dosage forms may exist for a single particular drug, since different medical conditions can warrant different routes of administration. For example, persistent nausea, especially with vomiting, may make it difficult to use an oral dosage form, and in such a case, it may be necessary to use an alternative route such as inhalational, buccal, sublingual, nasal, suppository or parenteral instead. Additionally, a specific dosage form may be a requirement for certain kinds of drugs, as there may be issues with various factors like chemical stability or pharmacokinetics. As an example, insulin cannot be given orally because upon being administered in this manner, it is extensively metabolized in the gastrointestinal tract (GIT) before reaching the blood stream, and is thereby incapable of sufficiently reaching its therapeutic target destinations. The oral and intravenous doses of a drug such as paracetamol will differ for the same reason
Analysis of parenteral dosage forms bjl final seminarPatel Parth
This document provides an overview of analytical testing for parenteral formulations. It discusses the need for quality assurance in parenterals due to risks of improper administration. The main types of parenterals are classified and key characteristics like sterility are outlined. Analytical methods for raw materials, finished products, and stability studies are summarized, including identification, potency, degradation products, pH and particulate testing. Microbiological tests like sterility and bacterial endotoxins are also covered at a high level.
'Rasasastra' ,is the science of metals , minerals , other toxic herbs , which are applied for attaining two goals. It is either used in the perspective of metallurgy, where lower metals are converted in to higher metals. It is otherwise used for the attainment of supreme health. This science , with both the applications were once well practiced in our country. But due to several factors, this divine science has been restricted to treatment aspect. 'Kshetreekarana' is the method of preparing the body to be eligible for administering processed divine mercury. In the midst various references Kshetreekarana generally , includes two steps. The first step is implementing Panchakarma therapy and second step involves administration of special formulations to attain a healthy condition to accept the divine mercury.
This document provides an overview of tablets as a pharmaceutical dosage form. It discusses the historical development of tablets, advantages and disadvantages, ideal tablet properties, and methods for evaluating tablets. Key aspects covered include tablet composition, compression, granulation, design and formulation. Evaluation methods summarized are general appearance, size and shape, identification markings, organoleptic properties, hardness and friability, drug content and release, weight uniformity, disintegration, and dissolution testing. The compression operation and basic components of tablet presses are also outlined.
This document discusses tablets as a dosage form for delivering medications. It defines tablets and outlines their advantages such as precise dosing, low cost, and stability. Various types of tablets are described based on where they are administered and how they release the drug. The key ingredients used in tablets called excipients are explained. Granulation techniques for tablet manufacturing like wet and dry granulation are summarized. The document also covers tablet processing problems that can occur and ways to control the manufacturing process.
Ayurveda strongly believes in using drugs with particular tastes in treating diseases. This presentation will help you understand the basics of rasa and its applied aspects in planning treatment protocol.
compilation of the inormation about Shilajeet/ salajeet from texts and internet. contents
classical references,
purification of Shilajeet,
medicinal uses of shilajeet,
Side effects of Shilajeet,
dose of Shilajeet,
aphrodisiac and other effects of Shilajeet
health benefits of shilajeet
chemical constituents of Shilajeet
Concept of Agni in Rasa Shastra & BhaishajyaNitika Rattan
Agni plays a key role in Ayurveda and Rasa Shastra. There are different types of Agni in the body and processes like Bhasmikaran use Agni to convert metals and minerals into microfine forms. Putas are methods of heating that are classified based on the level of heat intensity. Putas are an important part of the Marana process and influence the properties of the final Bhasma. Electric furnaces can now also be used as a controlled source of heat for Rasa Shastra procedures like Bhasmikaran.
Tablets are solid dosage forms made by compressing or molding mixtures of active and inactive ingredients. They are the most popular dosage form due to their accurate dosing, low cost, stability and ease of production. Tablets can be formulated for immediate or controlled release and come in various shapes, sizes and coatings. The manufacturing process involves mixing and granulating powders, then compressing them into tablets using either wet or dry granulation methods. Wet granulation is more common and involves using a liquid binder to form granules which are then dried, sized, lubricated and compressed. Tablets must balance physical attributes like strength with chemical properties like drug release.
The document provides details on quality control tests conducted on tablets, including physical tests like hardness, thickness, friability, and chemical tests like content uniformity and dissolution. It describes the purpose, equipment, and procedures for tests like hardness, thickness and diameter, friability, disintegration, weight variation, content uniformity, assay, and dissolution. The tests are essential to ensure tablets meet specifications for attributes like strength, thickness, ability to withstand abrasion, breakdown time, uniform drug content, and drug release rate.
tamra ppt new..pptx rasa shastra and bhaisajya kalpanarakhan78619
This document provides information about copper (tamra) including its Sanskrit and English names, chemical formula, properties, synonyms, geographical distribution, types, purification process, and methods of preparation as a bhasma for medicinal use according to classical Ayurvedic texts. Key points include that copper has high thermal and electrical conductivity, two types are distinguished based on source (Naipalika and Mleccha), and purification involves heating and dipping in specified liquids while preparation as a bhasma involves intricate multi-step processes including trituration and enclosure in pots for heating. The bhasma must then undergo an amritikarana process to remove toxicity before medicinal use.
Hard gelatin capsules are solid dosage forms where medicaments are enclosed in gelatin shells composed of two sections called caps and bodies. Capsules offer advantages like easy swallowing, taste masking, and protection from light. They are manufactured by dipping stainless steel pins in gelatin solution, spinning to distribute gelatin uniformly, drying, stripping caps and bodies, trimming, and joining. Capsules are filled using machines that separate caps from bodies, fill powder into bodies using various techniques like auger filling or piston tamping, scrape excess powder, replace caps, and seal capsules. Finished capsules are evaluated for tests like disintegration, dissolution, content uniformity and weight variation.
Quality Control Tests For Tablets and Capsules(QC)mdpavel
This document discusses quality control tests for tablets and capsules. It describes tests for general appearance, size, shape, thickness, color, and odor. It then compares quality control tests from the British, Indian, and United States Pharmacopoeias, including tests for content of active ingredients, disintegration, uniformity of content and weight, and labeling. Specific tests are described for different types of tablets, including uncoated, enteric coated, dispersible, and modified release tablets. Common non-official tests like hardness and friability are also summarized.
Santosh Kumar Tripathy is a DCDP currently working at Madinat Jumeirah in Dubai since 2016. He has over 10 years of experience in roles such as DCDP, Commis I, II, and III at hotels in Dubai, Ras Al Khaimah, Mumbai, and Hyderabad. He holds a diploma in F&B production from the Institute of Hotel Management in Bhubaneswar, India. His objective is to pursue a challenging career utilizing his education and skills to advance professionally and increase his knowledge.
אנחנו חיים בעולם מרובה ערוצים, מרובה מסכים, מרובה רשתות... המון קורה ובקצב מהיר. כולנו רוצים להיות מעודכנים בהכל עכשיו ומיד אבל בפועל אין לנו זמן... מקסימום יכולים לתפוס את ה"צינור".
בדיוק לשם כך, מחלקת מחקר אסטרטגי יצרה עבורכם את Spot‘it- סקירה שבועית שתאפשר לכם בצורה הפשוטה והקלה ביותר להתעדכן תוך מספר דקות בכל מה שחם ומעורר השראה בתרבות האינטרנט העכשווית.
ה-כול החל מסרטוני הרשת הוויראליים ביותר, פרסומות ומהלכים שיווקיים מעוררי השראה, הקליפים הנצפים ביותר, תכניות הטלוויזיה הכי מדוברות, הסרטים הכי חדשים ועוד, ועוד, ועוד...
Andrea Henderson is a multimedia journalist currently working at WLIO Hometown Stations where she conducts interviews, shoots and edits packages, and writes stories. She has previous experience in production roles at WSYX ABC6/WTTE FOX28, interned at multiple television stations, and worked as assistant multimedia editor for The Lantern student newspaper. Henderson graduated from Ohio State University in 2014 with a degree in journalism and a minor in media production.
The platform offers a native advertising solution that delivers higher click-through and conversion rates than banners. It has the largest coverage of native advertising in the UK, ensuring ROI. It guarantees performance and will refund fees if KPIs are not met. The platform provides maximum data resolution through campaign tagging, GA integration, and a bid data API to help users optimize success.
אנחנו חיים בעולם מרובה ערוצים, מרובה מסכים, מרובה רשתות... המון קורה ובקצב מהיר. כולנו רוצים להיות מעודכנים בהכל עכשיו ומיד אבל בפועל אין לנו זמן... מקסימום יכולים לתפוס את ה"צינור".
בדיוק לשם כך, מחלקת מחקר אסטרטגי יצרה עבורכם את Spot‘it- סקירה שבועית שתאפשר לכם בצורה הפשוטה והקלה ביותר להתעדכן תוך מספר דקות בכל מה שחם ומעורר השראה בתרבות האינטרנט העכשווית.
ה-כול החל מסרטוני הרשת הוויראליים ביותר, פרסומות ומהלכים שיווקיים מעוררי השראה, הקליפים הנצפים ביותר, תכניות הטלוויזיה הכי מדוברות, הסרטים הכי חדשים ועוד, ועוד, ועוד...
Helen Levitt foi uma fotógrafa americana nascida em 1913 conhecida por suas fotografias de rua em preto e branco de Nova Iorque, retratando crianças brincando e a vida cotidiana. Levitt estudou com fotógrafos renomados e trabalhou com cinema. Suas imagens imortalizaram a diversidade humana de forma espontânea.
This document provides instructions for a color theory assignment involving creating a 9-photo series following different color schemes in the style of Pop Art. Students are asked to take 9 portraits or photos on a single sheet following color combinations like primary colors, complementary colors, and triadic schemes. The photos can feature people, objects, or the same subject and must explore all 9 color schemes as directed. The assignment is due on March 4th.
This document discusses plans for unifying in-vehicle systems (IVS) in Russia, including the ERA-GLONASS emergency response system, fleet management systems, road tolling systems, and digital tachographs. The goals are to reduce costs by eliminating redundant hardware and functions across different IVS, standardize interfaces and communication protocols, and develop a single "connected IVS" approach. Key steps include developing standards for IVS/backend communication, regulations around unified use of GNSS data, and software/test tools to validate a reference implementation of unified protocols. Unifying these systems could lower total IVS costs per vehicle by at least 40% according to estimates.