Rxcare online pharmacy store in USA. Rxcare pharmacy Provide compounding-only pharmacy long trusted to provide the highest quality compounded medications.
The document discusses compounding, which involves preparing customized medications on demand according to a physician's prescription. It covers regulations, ingredients, equipment, dosage forms, labeling, and record keeping for compounding. Compounding allows for preparations tailored to individual patient needs like pediatric doses, alternative formulations for sensitivities, and specialized doses.
The document discusses various topics related to compounding medications, including regulations, equipment, and formulations. It covers the standards and guidelines for compounding from the United States Pharmacopeia, as well as how to properly use and calibrate important equipment like balances, mortar and pestles, and volumetric glassware. The document also reviews different dosage forms that are commonly compounded, such as solutions, suspensions, emulsions, ointments, and suppositories.
This document discusses techniques for compounding and good dispensing practices. It defines compounding as small-scale manufacturing of medicines from basic ingredients. Compounding should only be used when commercial medicines are unavailable. Proper organization, cleanliness, documentation, and appearance are important. A variety of equipment is used, including balances, measures, mortars and pestles, filters, and heat sources. Ingredients must be selected carefully. Counting devices like triangles and trays help accurately count tablets and capsules. Maintaining clean, methodical work is key to accurate extemporaneous dispensing.
USP <795> outlines responsibilities for compounders to produce medications of acceptable strength, quality, and purity with proper packaging and labeling according to laws and regulations. It describes compounding of nonsterile preparations and establishes categories of simple, moderate, and complex compounding based on the difficulty and potential risk of the preparations. USP 795 provides standards for nonsterile compounding that are enforceable by law to help ensure patient safety.
Pharmacy compounding - Importance, Non sterile compounding and Sterile compounding, Regulations of US Pharmacoepia, Compounded Products
For any suggestions and questions regarding this ppt please comment below.
Basic principles of compounding and dispensing (Prescription) MANIKImran Nur Manik
Weight, measure and units calculation for compounding and dispensing. Fundamental operation in compounding. Good pharmaceutical practices in compounding and dispensing. Containers and closures for dispensed products. Responding to prescription, labeling of dispensed medications.
This document outlines key concepts regarding compounding and repackaging of medications. It defines compounding as preparing medications tailored to individual patients. The document describes common compounding equipment, formulations like ointments and capsules, and the importance of record keeping. It also explains that repackaging involves transferring medications from bulk containers into individual patient packages, with proper packaging, labeling, and expiration dating required. Maintaining high quality practices through adherence to standards and regulations is emphasized.
Generic drugs and branded drugs can differ in excipients, coating, formulation, and production process, but must be bioequivalent to be interchangeable. Bioequivalence means there is no clinically significant difference in bioavailability, which is measured by the area under the blood concentration curve, maximum blood concentration, and time to maximum concentration. To be considered bioequivalent, these values must be within 20-25% for generic drugs compared to the branded reference drug. However, bioequivalence is only measured against the reference drug and differences may be larger when comparing different generic versions to each other or the original branded drug. Excipients can potentially affect bioequivalence, and narrow therapeutic index drugs require closer scrutiny due to smaller
The document discusses compounding, which involves preparing customized medications on demand according to a physician's prescription. It covers regulations, ingredients, equipment, dosage forms, labeling, and record keeping for compounding. Compounding allows for preparations tailored to individual patient needs like pediatric doses, alternative formulations for sensitivities, and specialized doses.
The document discusses various topics related to compounding medications, including regulations, equipment, and formulations. It covers the standards and guidelines for compounding from the United States Pharmacopeia, as well as how to properly use and calibrate important equipment like balances, mortar and pestles, and volumetric glassware. The document also reviews different dosage forms that are commonly compounded, such as solutions, suspensions, emulsions, ointments, and suppositories.
This document discusses techniques for compounding and good dispensing practices. It defines compounding as small-scale manufacturing of medicines from basic ingredients. Compounding should only be used when commercial medicines are unavailable. Proper organization, cleanliness, documentation, and appearance are important. A variety of equipment is used, including balances, measures, mortars and pestles, filters, and heat sources. Ingredients must be selected carefully. Counting devices like triangles and trays help accurately count tablets and capsules. Maintaining clean, methodical work is key to accurate extemporaneous dispensing.
USP <795> outlines responsibilities for compounders to produce medications of acceptable strength, quality, and purity with proper packaging and labeling according to laws and regulations. It describes compounding of nonsterile preparations and establishes categories of simple, moderate, and complex compounding based on the difficulty and potential risk of the preparations. USP 795 provides standards for nonsterile compounding that are enforceable by law to help ensure patient safety.
Pharmacy compounding - Importance, Non sterile compounding and Sterile compounding, Regulations of US Pharmacoepia, Compounded Products
For any suggestions and questions regarding this ppt please comment below.
Basic principles of compounding and dispensing (Prescription) MANIKImran Nur Manik
Weight, measure and units calculation for compounding and dispensing. Fundamental operation in compounding. Good pharmaceutical practices in compounding and dispensing. Containers and closures for dispensed products. Responding to prescription, labeling of dispensed medications.
This document outlines key concepts regarding compounding and repackaging of medications. It defines compounding as preparing medications tailored to individual patients. The document describes common compounding equipment, formulations like ointments and capsules, and the importance of record keeping. It also explains that repackaging involves transferring medications from bulk containers into individual patient packages, with proper packaging, labeling, and expiration dating required. Maintaining high quality practices through adherence to standards and regulations is emphasized.
Generic drugs and branded drugs can differ in excipients, coating, formulation, and production process, but must be bioequivalent to be interchangeable. Bioequivalence means there is no clinically significant difference in bioavailability, which is measured by the area under the blood concentration curve, maximum blood concentration, and time to maximum concentration. To be considered bioequivalent, these values must be within 20-25% for generic drugs compared to the branded reference drug. However, bioequivalence is only measured against the reference drug and differences may be larger when comparing different generic versions to each other or the original branded drug. Excipients can potentially affect bioequivalence, and narrow therapeutic index drugs require closer scrutiny due to smaller
This document discusses good dispensing practices for pharmacists. It covers interpreting prescriptions, packaging and labeling medications, and ensuring quality control. Efficient management is key, such as prepackaging common drugs and organizing workflow. Accuracy is prioritized over speed. Packaging must preserve drug stability and quality using appropriate materials like glass or plastic. Labels must clearly provide dosing instructions and patient information. Auxiliary labels may provide additional guidance. Prepackaging multi-dose therapies ensures accurate dosing and simplifies dispensing of complex regimens. Quality checks are necessary when repackaging to maintain expiration dates and product quality.
Chapter 11 Bulk repackaging and non-sterile compoundingPharmtechfau
The document discusses proper procedures for bulk repackaging and non-sterile compounding of medications. It describes the steps for bulk repackaging, including packaging one dose at a time, ensuring accurate labeling, and documenting the process. Reasons for bulk repackaging include medications that cannot be purchased from manufacturers and increased efficiency. The document also covers equipment and supplies used for non-sterile compounding, storage considerations, and techniques for accurately measuring and weighing ingredients.
This document provides an overview of pharmaceutical compounding and related topics. It discusses drugs and their sources, classifications, uses and dose forms. Key points include: drugs can come from natural, synthetic or semisynthetic sources; they are classified as over-the-counter, prescription, or controlled substances; and have therapeutic, diagnostic or preventative uses. Solid dose forms include tablets, capsules and other types; liquid forms include solutions and suspensions; and delivery systems can control drug release rates. The document aims to define important terms and compare different drug properties and formulations.
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 discusses in process quality control (IPQC) and finished product quality control (FPQC) tests for tablets. It begins with introducing the concepts of quality, quality control, IPQC and FPQC. It then lists and describes common tests conducted for tablets, including tests for size and shape, colour and odour, hardness, friability, content uniformity and dissolution. Standard acceptance criteria for many of the tests are also provided. The document emphasizes that IPQC and FPQC are important to control quality, identify errors, and ensure product specifications are met.
The document discusses in-process quality control (IPQC) for parenteral products. IPQC involves controlling manufacturing procedures from raw materials to finished product release. Key IPQC tests for parenterals include clarity testing to detect particulate matter using visual or automated methods, leakage testing of packaging, testing fill volume and pH, and sterility testing. The document outlines various physical, chemical, biological, and microbiological tests performed during IPQC to ensure product quality.
Sample preparation techniques of solid dosage formsSathish Vemula
Knife mills and blenders are particle size reduction techniques that can be used to disperse solid dosage forms like non-disintegrating tablets for analysis. Mechanical techniques like grinding with a mortar and pestle or milling in a ball mill are commonly used to reduce the particle size and facilitate extraction of drugs from solid oral dosage forms. Agitation techniques like shaking, stirring, vortexing, and sonication are then used to further facilitate dispersion and mixing during sample preparation. The selection of appropriate particle size reduction and agitation techniques depends on the properties of the specific drug product and dosage form being analyzed.
Ipqc tests for sterile formulations are as follows :
Leakage Test
Clarity Test
pH
Particulate Matter Injection
SterilityTest
Pyrogen Test
Content Uniformity & Weight
Volume Filled
The tests For Sterile products are as per IP, BP & USP
The document discusses the evaluation and testing of tablets. It describes non-official tests like general appearance, organoleptic properties, size and shape, hardness, and friability. It also describes official tests like weight variation, content uniformity, dissolution, and disintegration. It discusses different types of tablets like compressed and molded tablets. It provides details on evaluating the appearance, hardness, friability and other properties of tablets and describes tests like weight variation, content uniformity, and dissolution used to ensure tablets meet specifications.
IPQC Tests for capsules As per IP, BP & USPPramod Ramane
IPQC- In Process Quality Control Tests for Capsules are
1. Uniformity Of Content
2. Disintigration Test
3. Weight Variation Test
4. Dissolution Test
The tests are with Acceptance limits/Criteria as per Indian Pharmacopoeia (IP), British Pharmacopoeia (BP) & United States Pharmacopoeia (USP)
The document discusses the key aspects of a prescription, including:
- A prescription is a written order from a medical practitioner to a pharmacist to dispense a specific medication. It includes directions for use and administration.
- The main parts of a prescription include: date, patient information, drug names and quantities, directions for use, and prescriber information.
- When handling a prescription, pharmacists must carefully read, check ingredients, and label dispensed medications to avoid errors. Modern prescribing often involves proprietary drug names for ease of use, but official drug names are preferred. Abbreviations can introduce risks if not clearly understood.
IPQC and FPQC test for opthalmic preparation as per IP, BP ANIPQC D USProshan telrandhe
Ophthalmic preparation are the sterile liquid or semisolid preparation meant to installation in to the eyes in the space between eye lids and eye ball . These product must be sterile and are prepare under the same condition as that of parenteral preparation
This document provides information on quality management and quality control processes for pharmaceutical products. It discusses key concepts like quality assurance, quality control, quality management systems. It also summarizes the differences between quality assurance and quality control. The document then describes various quality control tests conducted on tablets and capsules, including tests of general appearance, hardness, friability, disintegration. It provides details on the purpose, procedures, and acceptance limits for these quality control tests.
This document discusses in-process quality control (IPQC) tests for parenteral products. It describes several key IPQC tests including drug content assays, clarity testing to detect particulate matter using various methods, leakage testing of ampoules using dye bath or spark tests, sterility testing using membrane filtration or direct inoculation methods, and endotoxin/pyrogen testing. Maintaining strict quality controls during manufacturing is important for ensuring parenterals are sterile, pyrogen-free, and free of particulate matter when injected into the body.
The presentation describes types advantages, disadvantages of parenteral preparations, route of administration, general requirement, evaluation, labeling & packaging, containers & their types etc
This document evaluates different parameters for testing tablets, including size, shape, hardness, friability, weight variation, disintegration, and dissolution. It discusses how these parameters are measured using various instruments and test methods. The key parameters are evaluated to ensure tablets meet specifications according to pharmacopoeia standards like the USP and IP.
Preparation and Evaluation of Aspirin tabletsSanket Kapadne
PREPARATION AND EVALUATION OF ASPIRIN TABLETS
Aim - Preparation and Evaluation of Aspirin Tablets.
Requirement –
Chemicals - Aspirin, HPMC, PVP, Sodium
Stearate, Talc
Glasswares - Granulating sieve, standard sieve set, etc.
Equipment - Tablet press
Principle
Aspirin tablet is prepared by wet granulation method. Aspirin belonging to the class of NSAID having analgesic, antipyretic, anti-inflammatory and antiplatelet activity at systematic standard doses. In this Lubricants in combination leads to better drug release kinetic. Aspirin tablets are obtained by wet Compression Method. The particles to be compressed consist of one or more medicaments, with or without excipients substance such as diluents, binders, and disintegration agents, lubricant, glidants.
Formula
Sr. No. Ingredients Quantity (1 Tab.)
1. Aspirin 250 mg
2. HPMC 50 mg
3. Microcrystalline Cellulose 70 mg
4. Polyvinyl Pyrrolidone Q.S.
5. Sodium Stearate+ Talc 1 mg + 5 mg
Method
Wet granulation forms the granulation by binding the powders together with an adheshive instead of by compaction.
Stages of granule development :
A. Pendular B. Funicular
C. Capillary D. Droplet Steps involved :
Step 1: Weighing and mixing of formulation ingredients.
Step 2: Preparing the damp mass.
Step 3: Screening the dampened powder into pellets or granules.
Step 4: Drying of moist granules.
Procedure
1. Tablets were prepared using wet granulation technique as per the composition given earlier.
2. The calculated amount which was required to prepare 400 mg aspirin tablets, containing 250 mg drug, HPMC polymer and PVP as a binder were mixed uniformly.
3. An enough granulating agent (water) was added slowly to prepare wet mass. Granules were prepared by sieving method using a 20# sieve.
4. Further, granules were dried at 35-45ºC for six hours. The dried granules were stored in desiccators until compression of tablets.
5.The required amounts of granules were weighed and compressed using automatically operated tablet punching machine having 12mm flat faced punch diameter and during the tablet preparation to maintain the low resistance between the solid and die wall, lubricants added in granules. Lubricant combinations are agents added in small quantities to the tablet during the tablet preparation.
6. The compressed tablets were stored in airtight container at room temperature for further evaluation.
Evaluation
1. Assay : Weigh and powder 20 tablets. Weigh accurately a quantity of the powder containing about 0.5 g of Aspirin, add 30.0 ml of 0.5M sodium hydroxide, boil gently for 10 minutes, cool and titrate the excess of alkali with 0.5 M hydrochloric acid using phenol red solution as indicator. Repeat the operation without the substance under examination. The difference
Premium pharmacy drawer systems, maximum storage space within a small footprint, metal product, long lasting and slick to use. Variety of sizes available. Store all sorts of medical devices, locking option available.
FPD Group Ltd supplies a range of pharmacy storage solutions including drawer systems, pullout shelves, and custom designs. They provide dispensary equipment, pharmacy shopfitting, and design services. The document provides information on their product lines, ordering process, exports, and installations.
This document discusses good dispensing practices for pharmacists. It covers interpreting prescriptions, packaging and labeling medications, and ensuring quality control. Efficient management is key, such as prepackaging common drugs and organizing workflow. Accuracy is prioritized over speed. Packaging must preserve drug stability and quality using appropriate materials like glass or plastic. Labels must clearly provide dosing instructions and patient information. Auxiliary labels may provide additional guidance. Prepackaging multi-dose therapies ensures accurate dosing and simplifies dispensing of complex regimens. Quality checks are necessary when repackaging to maintain expiration dates and product quality.
Chapter 11 Bulk repackaging and non-sterile compoundingPharmtechfau
The document discusses proper procedures for bulk repackaging and non-sterile compounding of medications. It describes the steps for bulk repackaging, including packaging one dose at a time, ensuring accurate labeling, and documenting the process. Reasons for bulk repackaging include medications that cannot be purchased from manufacturers and increased efficiency. The document also covers equipment and supplies used for non-sterile compounding, storage considerations, and techniques for accurately measuring and weighing ingredients.
This document provides an overview of pharmaceutical compounding and related topics. It discusses drugs and their sources, classifications, uses and dose forms. Key points include: drugs can come from natural, synthetic or semisynthetic sources; they are classified as over-the-counter, prescription, or controlled substances; and have therapeutic, diagnostic or preventative uses. Solid dose forms include tablets, capsules and other types; liquid forms include solutions and suspensions; and delivery systems can control drug release rates. The document aims to define important terms and compare different drug properties and formulations.
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 discusses in process quality control (IPQC) and finished product quality control (FPQC) tests for tablets. It begins with introducing the concepts of quality, quality control, IPQC and FPQC. It then lists and describes common tests conducted for tablets, including tests for size and shape, colour and odour, hardness, friability, content uniformity and dissolution. Standard acceptance criteria for many of the tests are also provided. The document emphasizes that IPQC and FPQC are important to control quality, identify errors, and ensure product specifications are met.
The document discusses in-process quality control (IPQC) for parenteral products. IPQC involves controlling manufacturing procedures from raw materials to finished product release. Key IPQC tests for parenterals include clarity testing to detect particulate matter using visual or automated methods, leakage testing of packaging, testing fill volume and pH, and sterility testing. The document outlines various physical, chemical, biological, and microbiological tests performed during IPQC to ensure product quality.
Sample preparation techniques of solid dosage formsSathish Vemula
Knife mills and blenders are particle size reduction techniques that can be used to disperse solid dosage forms like non-disintegrating tablets for analysis. Mechanical techniques like grinding with a mortar and pestle or milling in a ball mill are commonly used to reduce the particle size and facilitate extraction of drugs from solid oral dosage forms. Agitation techniques like shaking, stirring, vortexing, and sonication are then used to further facilitate dispersion and mixing during sample preparation. The selection of appropriate particle size reduction and agitation techniques depends on the properties of the specific drug product and dosage form being analyzed.
Ipqc tests for sterile formulations are as follows :
Leakage Test
Clarity Test
pH
Particulate Matter Injection
SterilityTest
Pyrogen Test
Content Uniformity & Weight
Volume Filled
The tests For Sterile products are as per IP, BP & USP
The document discusses the evaluation and testing of tablets. It describes non-official tests like general appearance, organoleptic properties, size and shape, hardness, and friability. It also describes official tests like weight variation, content uniformity, dissolution, and disintegration. It discusses different types of tablets like compressed and molded tablets. It provides details on evaluating the appearance, hardness, friability and other properties of tablets and describes tests like weight variation, content uniformity, and dissolution used to ensure tablets meet specifications.
IPQC Tests for capsules As per IP, BP & USPPramod Ramane
IPQC- In Process Quality Control Tests for Capsules are
1. Uniformity Of Content
2. Disintigration Test
3. Weight Variation Test
4. Dissolution Test
The tests are with Acceptance limits/Criteria as per Indian Pharmacopoeia (IP), British Pharmacopoeia (BP) & United States Pharmacopoeia (USP)
The document discusses the key aspects of a prescription, including:
- A prescription is a written order from a medical practitioner to a pharmacist to dispense a specific medication. It includes directions for use and administration.
- The main parts of a prescription include: date, patient information, drug names and quantities, directions for use, and prescriber information.
- When handling a prescription, pharmacists must carefully read, check ingredients, and label dispensed medications to avoid errors. Modern prescribing often involves proprietary drug names for ease of use, but official drug names are preferred. Abbreviations can introduce risks if not clearly understood.
IPQC and FPQC test for opthalmic preparation as per IP, BP ANIPQC D USProshan telrandhe
Ophthalmic preparation are the sterile liquid or semisolid preparation meant to installation in to the eyes in the space between eye lids and eye ball . These product must be sterile and are prepare under the same condition as that of parenteral preparation
This document provides information on quality management and quality control processes for pharmaceutical products. It discusses key concepts like quality assurance, quality control, quality management systems. It also summarizes the differences between quality assurance and quality control. The document then describes various quality control tests conducted on tablets and capsules, including tests of general appearance, hardness, friability, disintegration. It provides details on the purpose, procedures, and acceptance limits for these quality control tests.
This document discusses in-process quality control (IPQC) tests for parenteral products. It describes several key IPQC tests including drug content assays, clarity testing to detect particulate matter using various methods, leakage testing of ampoules using dye bath or spark tests, sterility testing using membrane filtration or direct inoculation methods, and endotoxin/pyrogen testing. Maintaining strict quality controls during manufacturing is important for ensuring parenterals are sterile, pyrogen-free, and free of particulate matter when injected into the body.
The presentation describes types advantages, disadvantages of parenteral preparations, route of administration, general requirement, evaluation, labeling & packaging, containers & their types etc
This document evaluates different parameters for testing tablets, including size, shape, hardness, friability, weight variation, disintegration, and dissolution. It discusses how these parameters are measured using various instruments and test methods. The key parameters are evaluated to ensure tablets meet specifications according to pharmacopoeia standards like the USP and IP.
Preparation and Evaluation of Aspirin tabletsSanket Kapadne
PREPARATION AND EVALUATION OF ASPIRIN TABLETS
Aim - Preparation and Evaluation of Aspirin Tablets.
Requirement –
Chemicals - Aspirin, HPMC, PVP, Sodium
Stearate, Talc
Glasswares - Granulating sieve, standard sieve set, etc.
Equipment - Tablet press
Principle
Aspirin tablet is prepared by wet granulation method. Aspirin belonging to the class of NSAID having analgesic, antipyretic, anti-inflammatory and antiplatelet activity at systematic standard doses. In this Lubricants in combination leads to better drug release kinetic. Aspirin tablets are obtained by wet Compression Method. The particles to be compressed consist of one or more medicaments, with or without excipients substance such as diluents, binders, and disintegration agents, lubricant, glidants.
Formula
Sr. No. Ingredients Quantity (1 Tab.)
1. Aspirin 250 mg
2. HPMC 50 mg
3. Microcrystalline Cellulose 70 mg
4. Polyvinyl Pyrrolidone Q.S.
5. Sodium Stearate+ Talc 1 mg + 5 mg
Method
Wet granulation forms the granulation by binding the powders together with an adheshive instead of by compaction.
Stages of granule development :
A. Pendular B. Funicular
C. Capillary D. Droplet Steps involved :
Step 1: Weighing and mixing of formulation ingredients.
Step 2: Preparing the damp mass.
Step 3: Screening the dampened powder into pellets or granules.
Step 4: Drying of moist granules.
Procedure
1. Tablets were prepared using wet granulation technique as per the composition given earlier.
2. The calculated amount which was required to prepare 400 mg aspirin tablets, containing 250 mg drug, HPMC polymer and PVP as a binder were mixed uniformly.
3. An enough granulating agent (water) was added slowly to prepare wet mass. Granules were prepared by sieving method using a 20# sieve.
4. Further, granules were dried at 35-45ºC for six hours. The dried granules were stored in desiccators until compression of tablets.
5.The required amounts of granules were weighed and compressed using automatically operated tablet punching machine having 12mm flat faced punch diameter and during the tablet preparation to maintain the low resistance between the solid and die wall, lubricants added in granules. Lubricant combinations are agents added in small quantities to the tablet during the tablet preparation.
6. The compressed tablets were stored in airtight container at room temperature for further evaluation.
Evaluation
1. Assay : Weigh and powder 20 tablets. Weigh accurately a quantity of the powder containing about 0.5 g of Aspirin, add 30.0 ml of 0.5M sodium hydroxide, boil gently for 10 minutes, cool and titrate the excess of alkali with 0.5 M hydrochloric acid using phenol red solution as indicator. Repeat the operation without the substance under examination. The difference
Premium pharmacy drawer systems, maximum storage space within a small footprint, metal product, long lasting and slick to use. Variety of sizes available. Store all sorts of medical devices, locking option available.
FPD Group Ltd supplies a range of pharmacy storage solutions including drawer systems, pullout shelves, and custom designs. They provide dispensary equipment, pharmacy shopfitting, and design services. The document provides information on their product lines, ordering process, exports, and installations.
The document provides profiles of students enrolled in the MBA program at NIPER, including their summer training experiences and credit seminar topics. It lists the names of over 20 students, the organizations they did their summer training at, and the topics of their credit seminars, which generally relate to the pharmaceutical industry. The profiles demonstrate the diverse experiences and areas of focus of NIPER's MBA students.
Pharmacy Storage & Pharmacy ShelvingY Series Pharmacy Drawer & Shelving UnitsA range of pharmacy storage and pharmacy shelving equipment designed specifically for dispensaries within pharmacies, hospitals and healthcare facilities.
All parts, including worksurfaces, are interchangeable so layouts can be amended at any time in the future to suit any changes in work flow or best practise.
Maximises stock density holding between three and four times the amount of stock held on traditional shelves.
•Increase dispensing efficiency
•Help to reduce selection errors
•Improve stock control
•Space saving system
•Simple to install
•Lowest prices
•Hard wearing and durable
•Easy to clean
Hospital Pharmacy Isolator Solutions for USP <797> Compliance from EscoEsco Group
The document discusses guidelines and regulations for handling hazardous drugs in hospitals, including USP <797>. It outlines the risks of exposure to hazardous drugs, such as cancer risks. Engineering controls are important for compounding sterile preparations to reduce contamination, including biological safety cabinets and compounding isolators. Personal protective equipment and proper work practices are also needed to safely handle hazardous drugs.
The document summarizes the requirements for an IV room project based on USP <797> standards. It discusses the primary engineering controls including laminar airflow workbenches and biological safety cabinets. It also outlines the architecture of buffer and ante areas, recommended devices for compounding, cleaning and disinfecting frequency guidelines, personnel hygiene and garbing procedures, packaging and labeling standards, and staff responsibilities. The IV room is designed to meet most USP requirements, with some exceptions like not fully separating the buffer and ante areas into different rooms.
Chemotherapy safety and handling-Thao's presentationHA VO THI
This document discusses chemotherapy safety and handling guidelines. It outlines the risks of hazardous drug exposure, engineering controls like ventilation requirements, personal protective equipment, safe storage, compounding and administration practices, decontamination procedures, medical surveillance, and future steps for improving safety in Vietnam. The key points are that chemotherapy drugs pose risks and strict protocols are needed to minimize exposure for healthcare workers handling these agents.
This document discusses various calculations used in sterile compounding. It covers learning objectives, types of calculations including basic formula, ratio and proportion, dimensional analysis, IV flow rates, IV drip rates, and alligations. It provides examples of how to perform each type of calculation and notes the specific scenarios where each method is best used. The goal is for readers to understand the principles and practice calculations to determine the correct method based on the medication and sterile compounding procedure.
The document provides an outline of topics covered in a chapter about institutional pharmacy. It discusses hospital pharmacy areas and services including unit dose distribution, repackaging, floor stock, and IV/TPN services. It also describes the roles of key hospital staff like pharmacists, nurses, physicians and technicians. The organization of medications in a hospital pharmacy is explained including storage by route of administration, refrigeration needs, and secure storage of controlled substances.
This document discusses intravenous admixture drugs prepared in hospital pharmacies. It defines admixture preparations as sterile IV solutions compounded using one or more medications or electrolytes to be administered parenterally. The document outlines the pharmacist's role in preparing, monitoring, and administering IV admixtures and parenteral drugs. It also describes the key components of an IV admixture pharmacy system, including the preparation area, storage area, policies and procedures for ensuring quality, stability, compatibility and reducing errors.
The document discusses hospital pharmacy services in India. It outlines the Pharmacy Act of 1948 and amendments that regulate pharmacy practice and qualifications. It describes the types of pharmacies and their functions, including dispensing medications, maintaining drug records, and ensuring quality. It also covers pharmacy planning, staffing, drug procurement, storage, and distribution to different hospital areas. The document notes challenges around drug pilferage, storage costs, and expired or outdated drugs.
DREAM DESIGNER (TIENS OPEN PLAN PRESENTAION) OPPDreamDesigner
TIENS International Pakistan Co.(Pvt)Ltd (hereinafter called TIENS Pakistan) is one of the 110 registered companies ,operating in Pakistan .
TIENS Pakistan was duly registered on Sept.20,2002 with Security Exchange Commission of Pakistan (SECP, registration No. K09031).TIENS Pakistan was also registered with Central Board of Revenue, with CBR NTN No.1452201-2.
TIENS Pakistan is also a registered m...ember of
Chamber of Commerce of Islamabad
Chamber of Commerce of
Chamber of Commerce of Karachi.
Chamber of Traders &Business Services
TIENS Pakistan is importing & marketing 285 varieties of quality products under the trade mark of TIENS in the following categories:
Healthcare food& supplements
Healthcare device &appliances
Beauty care & personal care products
House care products
All the TIENS quality products meet the most stringent quality standard in the world such as ISO,GMP,HACCP
It is worthwhile mentioning that the quality TINES healthcare food & supplements are herbal based natural dietary supplement, made in the TIENS production facilities in US,Malaysia ,and China.They are neither drugs nor medicines ,they are not covered under Drug Act 1976.The herbal based food supplements made in USA were FDA certified for free sales in US market,as well as for free export.
All the food supplements are Halal!
DREAM DESIGNER (TIENS OPEN PLAN PRESENTATION) OPPDreamDesigner
A high quality workforce of professional talents, together with a localized and well regulated management, has contributed to the internationally strategic goals of Tiens Group. In addition Tiens Group has an unbeatable international team in terms of research, innovation and professionalism, including more than 8,000 employees; 35% of which hold master's degree or higher.
Based on a complete operational management system and well-designed regulations, Tiens Group is marching into the Fortune 500 in big strides by relying on the remarkable theories such as "New Swap and Alternative Theory", "New Supermarket Theory", "Consumption Results Wealth" and "Operational Consumption Results More Wealth".
This document provides instructions for formulating and preparing a Ferrous Sulphate oral solution. It begins with an introduction on pharmaceutical syrups and describes Ferrous Sulphate as an iron supplement used to treat and prevent iron-deficiency anemia. The document then discusses anemia and provides a classification of anemia based on etiology. The remaining pages are presumed to provide the formula, ingredients, preparation method, and other details for a Ferrous Sulphate oral solution with each 5 ml containing 300 mg of Ferrous Sulphate BP.
The document discusses four ingredients in toothpaste that may contribute to weight gain: 1) Fluoride, which can disrupt thyroid function and metabolism; 2) Triclosan, an antibacterial agent that disrupts the endocrine system and can increase BMI; 3) Parabens, which mimic estrogen and have been shown to promote fat cell development; 4) Artificial sweeteners like saccharin, which provide empty calories and may disrupt metabolism. The document recommends checking toothpaste labels and avoiding products containing these four ingredients.
Sky Ways Health Care Private Limited is a pharmaceutical company located in Chandigarh, India that is seeking dedicated franchise partners. The company trades a wide range of pharmaceutical products including tablets, injections, capsules, syrups, suspensions and others. Under the guidance of managing director Mr. Munish Gupta, the company has maintained a strong presence in the pharmaceutical market and looks to expand its franchise partnerships.
The document discusses different types of tablets used in pharmaceutical applications. It begins by defining tablets as compressed solid dosage forms that can contain medicinal compounds with or without excipients. It then describes various characteristics of tablets including accurate dosing, uniform properties, and releasing drugs in a predictable manner. The document outlines different types of tablets like chewable, effervescent, lozenges, vaginal, and rectal tablets. It discusses how these tablets are formulated for specific routes of administration or uses. The document concludes by listing common excipients used in tablet formulations like diluents, binders, disintegrants, and lubricants along with their properties and functions.
The document discusses menopause and how it can impact sexual function and desire due to changes in hormone levels. It notes that while hormones play a role, other factors like relationships, mental health, and medication can also influence low sex drive. Treatment options presented include vaginal moisturizers, hormone replacement therapy (including local estrogen for vaginal symptoms), and potentially testosterone therapy under a doctor's guidance. Seeking help from a medical professional or therapist is encouraged to address both physical and psychological aspects.
The document discusses menopause and how it can impact sexual function and desire due to changes in hormone levels. It notes that while hormones play a role, other factors like relationships, mental health, and medication can also influence low sex drive. Treatment options presented include vaginal moisturizers, hormone replacement therapy (including local estrogen for vaginal symptoms), and potentially testosterone therapy under a doctor's guidance. Seeking help from a medical professional or therapist is encouraged to address both physical and psychological aspects.
This document discusses various life priorities and how the TIENS network can help achieve them. Some key priorities listed include having a business, a new house, car, better income, health and retirement. It then outlines the TIENS network structure and compensation plan, showing how one can progress from different ranks and earn bonuses and commissions. Finally, it highlights some popular TIENS products for health, beauty, weight loss and more, suggesting the network can help people enjoy a healthier, wealthier and prettier life.
This document reports on a student's industrial visit to the Uttar Pradesh Evertouch Healthcare Pharmacy in Kosi Kotwan, Mathura. It provides details on the company's facilities and production processes. The company produces various pharmaceutical dosage forms including tablets, capsules, syrups, and ayurvedic preparations. The report describes key production steps for these different forms such as granulation, blending, drying, punching, coating, filling capsules and syrups. It also discusses quality control processes to ensure product quality.
This document discusses the company Infinite Labs and their commitment to excellence in the sports nutrition industry. It provides the history of the company, noting it was founded in 2009 by an owner passionate about sports nutrition. It outlines the company's standards which are built around safety, as they refuse to include potentially harmful ingredients. It promises products that safely and effectively help customers achieve fitness goals. The document emphasizes their commitment to honesty, including testing of products to ensure labeling accuracy. It notes customers who are unsatisfied can return products for a refund to ensure satisfaction.
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A tablet is a compressed solid dosage form containing medicinal substances. Tablets can be immediate release, sustained release, enteric coated, film coated, or chewable. They are the most popular dosage form due to their convenience and stability. Tablets are manufactured through various processes including direct compression, dry granulation, and wet granulation. Wet granulation is commonly used and involves mixing, granulating with a binder solution, drying, milling, blending excipients, and compressing into tablets. Quality control of tablets involves testing parameters like weight, hardness, thickness, disintegration time, and friability.
Different types of drugs based on their respective functionsjosmonik
This document discusses different types of drugs that can cause tooth decay and their side effects. It provides examples of several common drugs that cause dry mouth and are linked to tooth decay, including antacids, pain medications, antihistamines, blood pressure medications, and antidepressants. It emphasizes the importance of consulting doctors about potential oral health side effects of medications and maintaining good oral hygiene practices.
Different types of drugs based on their respective functionsjos manik
This document summarizes different types of drugs that can cause tooth decay by producing dry mouth as a side effect. It discusses several classes of drugs like antacids, pain medications, antihistamines, high blood pressure medications, antidepressants, and corticosteroids that are known to cause dry mouth and increased risk of tooth decay. It emphasizes the importance of consulting doctors and dentists about oral health risks from long-term use of these medications and recommends practices like drinking water and proper brushing to prevent tooth decay.
Different types of drugs based on their respective functionsjosmonik
This document summarizes different types of drugs that can cause tooth decay by producing dry mouth as a side effect. It discusses several classes of drugs like antacids, pain medications, antihistamines, high blood pressure medications, antidepressants, and corticosteroids that are known to cause dry mouth and increased risk of tooth decay. It emphasizes the importance of consulting doctors and dentists about oral health risks from long-term use of these medications and recommends practices like drinking water and proper brushing to prevent tooth decay.
Therapeutics in dentistry(general principles)Iyad Abou Rabii
This document summarizes key principles of therapeutics in dentistry, including pharmacology basics like indications, contraindications, dose, and side effects. It discusses medication names, routes of drug administration, essential components of prescriptions, and Latin abbreviations commonly used. Key information covered includes Clark's Rule for calculating pediatric doses, factors to consider before prescribing drugs like interactions and patient factors, and legal responsibilities of the prescribing dentist.
This document provides information on monophasic liquid dosage forms. It defines monophasic forms as liquid preparations with only one phase, represented by a true solution. Advantages include easier swallowing and faster absorption than solids. Key considerations in formulation include drug solubility, choice of solvents, addition of preservatives, and maintaining stability. Proper manufacturing requires consideration of raw materials, equipment, and filling/packaging procedures. Common monophasic dosage forms include oral liquids like syrups and elixirs, and liquids for external use like mouthwashes and ointments.
This document discusses the formulation and evaluation of mouth dissolving tablets of Ondansetron HCL. It begins with an introduction to mouth dissolving tablets and their advantages over conventional tablets. It then provides drug information about Ondansetron HCL and discusses difficulties with existing oral dosage forms. The document describes the pre-compression and post-compression evaluation of 5 formulations of Ondansetron mouth dissolving tablets. It provides results of tests like hardness, friability, wetting time and drug content. The evaluation shows that the formulations complied with specifications for weight variation and drug content limits.
This document contains an overview of tablets and their uses in healthcare. It includes:
1. Lists of tablet types and their purposes such as treating conditions or providing nutrients.
2. Acknowledgments to individuals and organizations in Sweden that contribute to pharmaceutical research and healthcare.
3. A statement about how working together improves and saves lives through developing effective drug treatments.
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2. Rx Care Pharmacy
Locations
12071 Indian Rocks Road
Largo, FL
(727) 724-4171
1270 Malabar Road
Palm Bay, FL 32907
(321) 952-0656
13733 N US Highway 441
Lady Lake, FL 32159
(352) 391-5533
301 Havendale Boulevard
Auburndale, FL 33823
(863) 875-5700
725 US Highway 466
Lady Lake, FL 32159
(352) 633-2105
6018 The Plaza
Charlotte, NC 28215
(704) 531-5232
11304 Hawthorne Drive, Suite 120
Mint Hill, NC 28227
(704) 573-6899
16311 Grand River Avenue
Detroit, MI 48227
(313) 838-1100
1426 S Pine Avenue
Ocala, FL 34471
4160 Airline Drive
Bossier City, LA 71111
(318) 212-9990
5482 Rattlesnake Hammock Road
Naples, FL 34113
(239) 775-6800
421 9th Street N
Naples, FL 34102
(239) 262-2929
6350 Davis Boulevard
Naples, FL 34104
(239) 775-7207
3. What is Compounding?
Compounding is the art and
science of creating or
preparing personalized
medications for patients.
Individual ingredients are
combined in the exact
strength and dosage form
required by the patient. The
4. Is Compounding For Me?
Benefits Include:
• Ability to alter dosage form
• Ability to alter strength
• Avoid dyes, additives, fillers, preservatives or
sugars
• Ability to alter taste
• Avoid side effects
• Ability to create medicine that is no longer
commercially available
5.
6. We make compounds for…
Hospice Dental
Pain Management Dermatology
Podiatry Sports Medicine
Oncology Women’s Health
B.H.R.T. Men’s Health
Veterinary Pediatrics
Neuropathy Autism
7. Examples of
COMPOUNDING
for…
Hospice Podiatry
B.H.R.T Sports Medicine
Veterinary And much more…
Dental
8. •We can compound medication into various routes of
administration
•Pain management is personalized for the patient
•We offer treatments for:
Nausea/Vomiting
Pain Management
Mouth Ulcers
Saliva Stimulants
Radiation Burns
Adjunctive Therapy
Compounding/Hospice
9. •Therapy varies by patient, formulas are
customized based on needs
•Proven benefits
•Experience relief from:
Menopause
Hormonal Imbalance
Low Libido
Erectile Dysfunction
And Many More Symptoms…
Compounding/B.H.R.T.
10. •Ability to meet specific needs based on
varying weights and species
•Increased “patient” compliance due to
ability to alter form, taste and smell
•Ability to compound products no longer
commercially available
Compounding/Veterinary
11. We can compound…
•Hemostatics
•Bleaching Gels
•Dry Socket Compounds
•Root Canal Compounds
•Solutions for Mouth Ulcers
•Topical Anesthetics
•Pre-procedure Sedatives
•Antibiotics
•Adhesives
•Dry Mouth Solutions
Compounding/Dental
12. We offer compounded solutions for…
Muscle Spasms Jock Itch
Leg Cramps Nausea
Pain Sunburn
Bleeding Bruises
Athlete’s Foot Warts
Compounding/Sports Medicine
17. Benefits Include:
Convert Other Dosage Forms to
Liquid for Patients Who Cannot
Swallow Pills, such as:
• Pediatrics
• Geriatrics
Avoid Unwanted Ingredients, such
as:
• Dyes
• Preservatives
• Alcohols
• Sugars
Increase Patient
Compliance with:
• Flavor Options
18. Benefits Include:
o Can be used for systemic OR local issues
o Beneficial for patients who cannot swallow
o Effective absorption allows medicine to start working
quickly
o Avoid negative gastrointestinal effects
19. Benefits Include:
•Increased Patient Compliance
Flavor Options
•Excellent Results as a Smoking Cessation
•Popular for Pediatric Patients
21. Rectal or Vaginal Use
Excellent Solutions for Patients
Experiencing Nausea/Vomiting
Rapid Effect on Conditions Such as IBS,
Hemorrhoids and Chrohn’s Disease
Good Choice for Patients with Difficulty
Swallowing
22. Benefits Include:
Increased Compliance in Patients
Avoiding Oral Administration
Avoid Gastrointestinal Effects
Increased Effectiveness Due to Direct
Application
Easy Self-Administration in ‘As Needed’
Doses
Available Forms: Cream ∙ Gel ∙ Ointment ∙ Spray ∙ Deodorant Lip Balm
24. This machine
is used for
compounding
capsules. It
allows
capsules to
be made free
of dyes and
fillers!
25. The Troche Mold
holds troches while
they cool and take
on their final form.
Troches provide
rapid sublingual
administration of
medicine. Many
flavors are
available at the
26. The Sterile Glovebox provides the pharmacist with
an isolated environment in which he can compound
sterile products.
27. This mold ensures the proper amount of
liquid is used in each lollipop.
It holds the stick in place while the liquid
hardens.
28. An Ointment Mill is
used to reduce
particle size in
compounded
products. Creams
and ointments are
ground through
porcelain rollers to
ensure fine particle
size. Smallest
possible particle size
is desired so that
30. This mold ensures the proper
amount of ingredients is used for
each suppository. We can
compound rectal and vaginal
suppositories.
31. A hood is used to
control airborne
powder particles.
It provides a safe
environment for
pharmacists and
technicians to
handle the
ingredients of a
compounded
32. Questions?
For more information or to speak to a pharmacist,
please call Rx Care Pharmacy to be directed to
the location nearest you!
Call us at (813) 304-2221