Harikrushna Machines Machinery Company share the slide information on the liquid filling machine including what is liquid filler machine, the importance of the liquid filling machine, the types of liquid filling machines, how to buy liquid filling machines, etc.
1) Blow fill seal technology is used to aseptically produce small liquid-filled containers through continuous formation, filling, and sealing processes.
2) Jet injectors administer injections through compressed gas that forms a narrow, high-pressure jet instead of using hypodermic needles.
3) Both technologies offer sterile, safe administration of drugs without using needles and are useful for mass vaccinations.
Basics of Automation in Solid Dosage Form Production (Formulation & Developem...Vishal Shelke
Basics of Automation in Solid Dosage Form Production by Mr. Vishal Shelke(Formulation & Developement M.Pharm Sem II)
https://youtube.com/vishalshelke99
https://instagram.com/vishal_stagram
Sub :- Formulation & Developement
M.Pharm Sem II
Savitribai Phule Pune University
This document provides guidance on validating a liquid filling and sealing machine. It discusses the key stages of validation including user requirement specification, design qualification, installation qualification, operational qualification, and performance qualification. The performance qualification section provides specific tests to validate the machine's weight variation, filling volume accuracy, particle contamination levels, leak testing, and oxygen content. Requalification of the machine is recommended on a defined schedule or after any changes to ensure continued proper operation.
This document provides an overview of pharmaceutical documentation and quality control processes. It discusses the importance of documentation in areas like manufacturing, batch records, and quality control. The key points covered are:
- Pharmaceutical documentation includes master formulas, batch records, quality control records, and distribution records.
- Documents must be properly controlled and approved to ensure accurate information. Controlled documents are identified, dated, approved, and retained for a specified period.
- Batch records are built from approved master formulas and provide a history of each batch production for quality purposes. They include processing details, materials used, equipment, and lab results.
- Quality control documentation helps ensure compliance and that products meet specifications. Proper documentation is
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.
Technology Transfer in Pharma Industry, Technology Transfer in Pharmaceutical Industry, Pharmaceutical Technology Transfer, Pharma Tech Transfer, Naseeb basha, Pharmaceutical Tech Transfer, Naseeb basha Technology Transfer in Pharma Industry, Naseeb basha Pharmaceutical Technology Transfer
This document discusses quality control tests for various types of surgical dressings. It describes different types of surgical dressings classified based on function and materials used. Tests are outlined to identify materials like cotton and wool that are commonly used in dressings. These include absorbency, fluorescence and solubility tests. Additional tests for finished products are also summarized, such as count of threads, weight, tensile strength and tests to check for foreign matter and water soluble extractives. Rubber and oil impregnated dressings are also briefly discussed.
Regulatory requirements of row countriesDivya Pushp
This document provides an overview of regulatory requirements for pharmaceutical registration in Rest of World (ROW) countries. It begins with definitions of ROW countries and importance of harmonization. It then discusses differences between regulated and emerging markets and provides a comparative study of registration requirements across various regions including ASEAN, GCC, Latin America, CIS, Asia Pacific and Africa. Key requirements discussed include administrative documents, chemistry manufacturing and controls, specifications, stability data, packaging and labeling. Common queries from ROW countries are also summarized.
1) Blow fill seal technology is used to aseptically produce small liquid-filled containers through continuous formation, filling, and sealing processes.
2) Jet injectors administer injections through compressed gas that forms a narrow, high-pressure jet instead of using hypodermic needles.
3) Both technologies offer sterile, safe administration of drugs without using needles and are useful for mass vaccinations.
Basics of Automation in Solid Dosage Form Production (Formulation & Developem...Vishal Shelke
Basics of Automation in Solid Dosage Form Production by Mr. Vishal Shelke(Formulation & Developement M.Pharm Sem II)
https://youtube.com/vishalshelke99
https://instagram.com/vishal_stagram
Sub :- Formulation & Developement
M.Pharm Sem II
Savitribai Phule Pune University
This document provides guidance on validating a liquid filling and sealing machine. It discusses the key stages of validation including user requirement specification, design qualification, installation qualification, operational qualification, and performance qualification. The performance qualification section provides specific tests to validate the machine's weight variation, filling volume accuracy, particle contamination levels, leak testing, and oxygen content. Requalification of the machine is recommended on a defined schedule or after any changes to ensure continued proper operation.
This document provides an overview of pharmaceutical documentation and quality control processes. It discusses the importance of documentation in areas like manufacturing, batch records, and quality control. The key points covered are:
- Pharmaceutical documentation includes master formulas, batch records, quality control records, and distribution records.
- Documents must be properly controlled and approved to ensure accurate information. Controlled documents are identified, dated, approved, and retained for a specified period.
- Batch records are built from approved master formulas and provide a history of each batch production for quality purposes. They include processing details, materials used, equipment, and lab results.
- Quality control documentation helps ensure compliance and that products meet specifications. Proper documentation is
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.
Technology Transfer in Pharma Industry, Technology Transfer in Pharmaceutical Industry, Pharmaceutical Technology Transfer, Pharma Tech Transfer, Naseeb basha, Pharmaceutical Tech Transfer, Naseeb basha Technology Transfer in Pharma Industry, Naseeb basha Pharmaceutical Technology Transfer
This document discusses quality control tests for various types of surgical dressings. It describes different types of surgical dressings classified based on function and materials used. Tests are outlined to identify materials like cotton and wool that are commonly used in dressings. These include absorbency, fluorescence and solubility tests. Additional tests for finished products are also summarized, such as count of threads, weight, tensile strength and tests to check for foreign matter and water soluble extractives. Rubber and oil impregnated dressings are also briefly discussed.
Regulatory requirements of row countriesDivya Pushp
This document provides an overview of regulatory requirements for pharmaceutical registration in Rest of World (ROW) countries. It begins with definitions of ROW countries and importance of harmonization. It then discusses differences between regulated and emerging markets and provides a comparative study of registration requirements across various regions including ASEAN, GCC, Latin America, CIS, Asia Pacific and Africa. Key requirements discussed include administrative documents, chemistry manufacturing and controls, specifications, stability data, packaging and labeling. Common queries from ROW countries are also summarized.
This document discusses process validation for solid oral dosage forms such as tablets and capsules. It begins by defining process validation and outlining the types, including prospective, concurrent, and retrospective validation. For tablets, it covers validation of raw materials, analytical methods, equipment, and process parameters. For capsules, it discusses validation of the capsule composition, encapsulation process, and quality control tests. The conclusion emphasizes that validation ensures reproducibility and compliance.
The document discusses the design and layout considerations for pharmaceutical manufacturing facilities. It states that premises should be located to minimize risks of cross-contamination from external sources. The interior surfaces should be smooth and allow for easy cleaning. Specific areas for different processes like manufacturing, packaging, laboratories should be separated but laid out in a logical flow. Material and personnel flow should be organized to prevent mix-ups and cross-contamination. Tables and figures provide examples of suitable layouts for manufacturing tablets and liquid oral preparations.
Validation is the process of checking of the process, equipment and method whereas qualification is solely done for equipment and qualification of instrument helps in quality of pharmaceutical product.
Pharmaceutical packaging serves several important functions:
1) It identifies and protects pharmaceutical products, facilitating their safe use by consumers.
2) Common packaging materials include glass, plastics, rubber, metals, and paper which are chosen based on their ability to protect contents and compatibility with dosage forms.
3) Packaging is tested to ensure it can withstand impacts and stresses of distribution while maintaining product integrity.
ICH Q8 GUIDELINES OF QUALITY BY DESIGN(PRODUCT DEVELOPEMENT)ROHIT
This document presents an overview of ICH Q8 guidelines for pharmaceutical product development using Quality by Design (QbD) principles. It discusses key QbD concepts like Quality Target Product Profile, critical quality attributes, critical process parameters, and design space. The document also summarizes the contents that should be included in the CTD quality module regarding drug substances, formulation development, manufacturing process, container closure system, microbiological attributes, and compatibility studies. Finally, it emphasizes that QbD ensures quality is built into the product design rather than relying solely on end-product testing.
1) Tablet manufacturing has advanced with new material handling, raw materials, granulation, coating, and compression technologies that improve efficiency and quality.
2) Advancements include direct compression excipients, dry and melt granulation methods, all-in-one systems, and single-step tablet coating and manufacturing processes.
3) New equipment allows for automated and continuous processing with improved control and monitoring from granulation to finished tablets.
Validation: Validation is a documented program that provides high degree of assurance that a specific process, method or system consistently produces a result meeting pre-determined acceptance criteria.
This document discusses stability testing of pharmaceutical packaging. Stability testing ensures that packaging maintains the quality of drugs over time under various environmental conditions like temperature, humidity and light. It involves testing packaging for leakage, strength, impact of distribution processes, and compatibility with drugs. The document outlines guidelines for conducting stability tests, including storage conditions, timepoints for sampling, and parameters to evaluate like appearance, assay and degradation. The goal is to determine shelf life and ensure patient safety.
This document provides information about qualification of an autoclave. It defines qualification as proving that equipment works correctly and leads to expected results. It discusses different types of qualification including design, installation, operational, and performance qualification. For autoclave qualification, it outlines tests that should be performed at each stage like temperature mapping, alarm checks, steam penetration tests, and biological indicator testing to prove the autoclave is sterilizing properly. It also provides guidelines for safe operation of the autoclave.
ManageArtworks is a Cloud based Packaging Artwork Management and Labeling Software which helps Pharma, Food and Cosmetic companies gain a competitive edge.
plastic and glass containers and its evaluation test, drug plastic considera...SUJIT DAS
This document discusses quality control tests that must be conducted on plastic containers used for pharmaceutical products. It outlines specific tests for non-parenteral and parenteral preparations, including leakage tests, clarity of extracts, and limits for substances like barium, heavy metals, and tin. It also discusses considerations for using plastic versus glass containers, noting potential issues like permeation of gases/liquids, leaching of substances from the plastic, and chemical reactions between drugs and container materials.
The Therapeutic Goods Administration or TGA is the regulatory body for therapeutic goods in Australia.
The TGA is responsible for conducting assessment and monitoring activities to ensure that therapeutic goods available in Australia are of an acceptable standard.
This document provides an overview of the formulation and development of parenteral products. It discusses the key components including containers, closures, processing, formulation, production facilities, and evaluation methods. The production area is divided into five sections - cleanup, preparation, aseptic, quarantine, and finishing/packaging areas. Parenteral formulations contain active drugs, vehicles, and adjuvants. Finished products undergo sterility, clarity, leakage, pyrogen, and assay testing to ensure quality control.
Process validation of liquid orals (pharmaceutical process validation)sarikakkadam
This document discusses process validation for liquid oral drug products such as suspensions and emulsions. It describes the key unit operations involved in manufacturing such products including mixing, blending, and dispersing. It identifies important process parameters for each unit operation that can influence critical quality attributes. It also discusses monitoring of critical quality attributes like appearance, pH, viscosity and content uniformity. Finally, it covers validation of raw materials and filling/packaging operations for liquid oral products.
Pharmaceutical development report (pdr)Atul Bhombe
The document discusses the key sections and guidelines for an effective Pharmaceutical Development Report (PDR) as outlined in ICH Q8 and Q8(R1). The six critical sections of a PDR are: 1) active and inactive ingredients, 2) formulation development and properties, 3) manufacturing process development, 4) container closure system, 5) microbiological attributes, and 6) compatibility with diluents. The PDR provides a comprehensive understanding of the product and manufacturing process for regulatory review and should be updated throughout the product lifecycle.
This document discusses Process Analytical Technology (PAT). It begins with an introduction to PAT, defining it as a system to design, analyze, and control manufacturing through timely measurements of critical quality attributes. It then discusses how PAT works by selecting a suitable PAT system and identifying critical process parameters. It highlights some key benefits of PAT such as improving process understanding and control, enhancing safety, and reducing variation. The document also provides examples of common PAT applications and discusses regulatory guidance around implementing PAT from agencies like the FDA.
This document discusses the process validation of capsules. It begins by providing background on validation and defining process validation according to the FDA. It then describes the three main types of process validation: prospective, concurrent, and retrospective. Key documents used in validation like the validation master plan, validation protocols and reports, and standard operating procedures are also outlined. The validation process for capsules is then detailed, including evaluating the capsule composition, selecting the encapsulation process and equipment, and testing the encapsulation step. Critical factors considered during encapsulation like the technique used and encapsulation speed are also summarized.
This document discusses pharmaceutical packaging materials and their evaluation. It introduces the need for packaging in protecting pharmaceutical products and providing information. The main types of primary packaging materials discussed are glass, plastics, metals, films and foils, elastomeric closures. Secondary and tertiary packaging materials are also mentioned. Various tests for evaluating the different materials are summarized such as permeability and mechanical tests.
Pharmaceutical Production Planning and controlRaviTeja Netha
Production planning and control is important for pharmaceutical manufacturing. It involves preparing detailed plans to manufacture products on time and within budget. Production control ensures quality standards are met. There are different types of production systems like continuous and intermittent. Planning includes selecting materials, processes, equipment and layout. Routing defines the sequence of operations. Scheduling optimizes production costs. Progress reports are analyzed and corrective actions taken if needed to resolve issues and ensure targets are met. The overall goal is efficient and effective pharmaceutical production.
HMPL IS A PROUD INDIAN ORGANIZATION INCEPTED
BY MR. MAULIK V. DAVE IN 1999-2000.
Harikrushna Machines Excels in Offering Complete Liquid Processing & Liquid Packaging Solutions to Segments Like Beverages, Chemicals, Cosmetics, Dairy, Detergents, Distilleries, Edible Oil, Fertilizers, Food, Nutraceuticals, Paints, Pharmaceutical, Lubricants Oil, Pesticides, Pigments, Plastics, and Other Liquid-based Manufacturing Industries
HMPL Spectrum of Liquid Products Includes Various Washing Machines, Filling Machines, Plugging, Sealing and Capping Machines, Labeling Machines and Special Purpose Machines Like Automatic Shrink Sleeve Applicator, Trio-block 3 in 1 (Rinsing, Filling and Capping), Automatic Mosquito Replant Packing Systems, Flavored Milk/Plain Milk Packaging System and Pre-Filled Syringe Filling and Stoppering Machine.
HMPL Spectrum of Processing Solution Includes Various Liquid Oral/syrup Manufacturing Plant, Ointment/Lotion/Cream/Toothpaste Manufacturing Plant, Various Application Mixer Machine Like Juice, Paint, Gel, Milk, Curd, Etc.
This document discusses process validation for solid oral dosage forms such as tablets and capsules. It begins by defining process validation and outlining the types, including prospective, concurrent, and retrospective validation. For tablets, it covers validation of raw materials, analytical methods, equipment, and process parameters. For capsules, it discusses validation of the capsule composition, encapsulation process, and quality control tests. The conclusion emphasizes that validation ensures reproducibility and compliance.
The document discusses the design and layout considerations for pharmaceutical manufacturing facilities. It states that premises should be located to minimize risks of cross-contamination from external sources. The interior surfaces should be smooth and allow for easy cleaning. Specific areas for different processes like manufacturing, packaging, laboratories should be separated but laid out in a logical flow. Material and personnel flow should be organized to prevent mix-ups and cross-contamination. Tables and figures provide examples of suitable layouts for manufacturing tablets and liquid oral preparations.
Validation is the process of checking of the process, equipment and method whereas qualification is solely done for equipment and qualification of instrument helps in quality of pharmaceutical product.
Pharmaceutical packaging serves several important functions:
1) It identifies and protects pharmaceutical products, facilitating their safe use by consumers.
2) Common packaging materials include glass, plastics, rubber, metals, and paper which are chosen based on their ability to protect contents and compatibility with dosage forms.
3) Packaging is tested to ensure it can withstand impacts and stresses of distribution while maintaining product integrity.
ICH Q8 GUIDELINES OF QUALITY BY DESIGN(PRODUCT DEVELOPEMENT)ROHIT
This document presents an overview of ICH Q8 guidelines for pharmaceutical product development using Quality by Design (QbD) principles. It discusses key QbD concepts like Quality Target Product Profile, critical quality attributes, critical process parameters, and design space. The document also summarizes the contents that should be included in the CTD quality module regarding drug substances, formulation development, manufacturing process, container closure system, microbiological attributes, and compatibility studies. Finally, it emphasizes that QbD ensures quality is built into the product design rather than relying solely on end-product testing.
1) Tablet manufacturing has advanced with new material handling, raw materials, granulation, coating, and compression technologies that improve efficiency and quality.
2) Advancements include direct compression excipients, dry and melt granulation methods, all-in-one systems, and single-step tablet coating and manufacturing processes.
3) New equipment allows for automated and continuous processing with improved control and monitoring from granulation to finished tablets.
Validation: Validation is a documented program that provides high degree of assurance that a specific process, method or system consistently produces a result meeting pre-determined acceptance criteria.
This document discusses stability testing of pharmaceutical packaging. Stability testing ensures that packaging maintains the quality of drugs over time under various environmental conditions like temperature, humidity and light. It involves testing packaging for leakage, strength, impact of distribution processes, and compatibility with drugs. The document outlines guidelines for conducting stability tests, including storage conditions, timepoints for sampling, and parameters to evaluate like appearance, assay and degradation. The goal is to determine shelf life and ensure patient safety.
This document provides information about qualification of an autoclave. It defines qualification as proving that equipment works correctly and leads to expected results. It discusses different types of qualification including design, installation, operational, and performance qualification. For autoclave qualification, it outlines tests that should be performed at each stage like temperature mapping, alarm checks, steam penetration tests, and biological indicator testing to prove the autoclave is sterilizing properly. It also provides guidelines for safe operation of the autoclave.
ManageArtworks is a Cloud based Packaging Artwork Management and Labeling Software which helps Pharma, Food and Cosmetic companies gain a competitive edge.
plastic and glass containers and its evaluation test, drug plastic considera...SUJIT DAS
This document discusses quality control tests that must be conducted on plastic containers used for pharmaceutical products. It outlines specific tests for non-parenteral and parenteral preparations, including leakage tests, clarity of extracts, and limits for substances like barium, heavy metals, and tin. It also discusses considerations for using plastic versus glass containers, noting potential issues like permeation of gases/liquids, leaching of substances from the plastic, and chemical reactions between drugs and container materials.
The Therapeutic Goods Administration or TGA is the regulatory body for therapeutic goods in Australia.
The TGA is responsible for conducting assessment and monitoring activities to ensure that therapeutic goods available in Australia are of an acceptable standard.
This document provides an overview of the formulation and development of parenteral products. It discusses the key components including containers, closures, processing, formulation, production facilities, and evaluation methods. The production area is divided into five sections - cleanup, preparation, aseptic, quarantine, and finishing/packaging areas. Parenteral formulations contain active drugs, vehicles, and adjuvants. Finished products undergo sterility, clarity, leakage, pyrogen, and assay testing to ensure quality control.
Process validation of liquid orals (pharmaceutical process validation)sarikakkadam
This document discusses process validation for liquid oral drug products such as suspensions and emulsions. It describes the key unit operations involved in manufacturing such products including mixing, blending, and dispersing. It identifies important process parameters for each unit operation that can influence critical quality attributes. It also discusses monitoring of critical quality attributes like appearance, pH, viscosity and content uniformity. Finally, it covers validation of raw materials and filling/packaging operations for liquid oral products.
Pharmaceutical development report (pdr)Atul Bhombe
The document discusses the key sections and guidelines for an effective Pharmaceutical Development Report (PDR) as outlined in ICH Q8 and Q8(R1). The six critical sections of a PDR are: 1) active and inactive ingredients, 2) formulation development and properties, 3) manufacturing process development, 4) container closure system, 5) microbiological attributes, and 6) compatibility with diluents. The PDR provides a comprehensive understanding of the product and manufacturing process for regulatory review and should be updated throughout the product lifecycle.
This document discusses Process Analytical Technology (PAT). It begins with an introduction to PAT, defining it as a system to design, analyze, and control manufacturing through timely measurements of critical quality attributes. It then discusses how PAT works by selecting a suitable PAT system and identifying critical process parameters. It highlights some key benefits of PAT such as improving process understanding and control, enhancing safety, and reducing variation. The document also provides examples of common PAT applications and discusses regulatory guidance around implementing PAT from agencies like the FDA.
This document discusses the process validation of capsules. It begins by providing background on validation and defining process validation according to the FDA. It then describes the three main types of process validation: prospective, concurrent, and retrospective. Key documents used in validation like the validation master plan, validation protocols and reports, and standard operating procedures are also outlined. The validation process for capsules is then detailed, including evaluating the capsule composition, selecting the encapsulation process and equipment, and testing the encapsulation step. Critical factors considered during encapsulation like the technique used and encapsulation speed are also summarized.
This document discusses pharmaceutical packaging materials and their evaluation. It introduces the need for packaging in protecting pharmaceutical products and providing information. The main types of primary packaging materials discussed are glass, plastics, metals, films and foils, elastomeric closures. Secondary and tertiary packaging materials are also mentioned. Various tests for evaluating the different materials are summarized such as permeability and mechanical tests.
Pharmaceutical Production Planning and controlRaviTeja Netha
Production planning and control is important for pharmaceutical manufacturing. It involves preparing detailed plans to manufacture products on time and within budget. Production control ensures quality standards are met. There are different types of production systems like continuous and intermittent. Planning includes selecting materials, processes, equipment and layout. Routing defines the sequence of operations. Scheduling optimizes production costs. Progress reports are analyzed and corrective actions taken if needed to resolve issues and ensure targets are met. The overall goal is efficient and effective pharmaceutical production.
HMPL IS A PROUD INDIAN ORGANIZATION INCEPTED
BY MR. MAULIK V. DAVE IN 1999-2000.
Harikrushna Machines Excels in Offering Complete Liquid Processing & Liquid Packaging Solutions to Segments Like Beverages, Chemicals, Cosmetics, Dairy, Detergents, Distilleries, Edible Oil, Fertilizers, Food, Nutraceuticals, Paints, Pharmaceutical, Lubricants Oil, Pesticides, Pigments, Plastics, and Other Liquid-based Manufacturing Industries
HMPL Spectrum of Liquid Products Includes Various Washing Machines, Filling Machines, Plugging, Sealing and Capping Machines, Labeling Machines and Special Purpose Machines Like Automatic Shrink Sleeve Applicator, Trio-block 3 in 1 (Rinsing, Filling and Capping), Automatic Mosquito Replant Packing Systems, Flavored Milk/Plain Milk Packaging System and Pre-Filled Syringe Filling and Stoppering Machine.
HMPL Spectrum of Processing Solution Includes Various Liquid Oral/syrup Manufacturing Plant, Ointment/Lotion/Cream/Toothpaste Manufacturing Plant, Various Application Mixer Machine Like Juice, Paint, Gel, Milk, Curd, Etc.
The Bottle Capping Machine designed by us, a leading manufacturer, supplier, and exporter has unique features which make the automatic bottle capping machine compatible and user-friendly.
This document provides information about a company that manufactures and exports liquid packaging machinery. It describes various machines for washing, filling, capping, labeling, and packaging liquids. The company serves industries such as pharmaceuticals, cosmetics, dairy, food, and more. It has over 10,000 installations worldwide and manufactures machines that meet international certifications. The document includes technical specifications, photos, and contact information.
This document provides information about a company that manufactures and exports liquid packaging machinery. It describes various machines for washing, filling, capping, labeling, and packaging liquids. The company serves industries such as pharmaceuticals, cosmetics, dairy, food, and more. It has over 10,000 installations worldwide and manufactures machines that meet international certifications. The document includes technical specifications and photos for the different machine types.
This document provides information about a company that manufactures and exports liquid packaging machinery. It describes various machines for washing, filling, capping, labeling, and packaging liquids. The company serves industries such as pharmaceuticals, cosmetics, dairy, food, and more. It has over 10,000 installations worldwide and manufactures machines that meet international certifications. The document includes technical specifications, photos, and contact information.
Milk line for glass and pet milk bottles line consists of washing, filling, crown capping/screw capping, conduction/induction cap sealing, labeling/shrink sleeve applicator, packing conveyor, web sealer for group packing
HARIKRUSHNA Milk Packing linefor Glass and PP Bottles which includes Washing, Filling, Capping, Induction Or Conduction Sealing, Leack Check Machine For The Bottle, Shrink Sleeve Label Applicator & Case Packer. All machines are with unique design and features.
For flavored milk, our Glass and PP Line are working in different dairies. Few of the reference customers are as under.
Automatic Sticker Labeling System consists of main structure, covered with SS cabinet and safety acrylic doors (OPTIONAL), product transmission belt with adjustable guide, separator unit, label dispenser unit, label wrapping unit, electrical panel, PLC HMI, AC drives a batch printing unit(OPTIONAL). The complete operation is PLC based.
This document provides information about a company that manufactures and exports liquid packaging machinery. It describes various machines for washing, filling, capping, labeling, and packaging liquids. The company serves industries such as pharmaceuticals, cosmetics, dairy, food, and more. It has over 10,000 installations worldwide and manufactures machines that meet international certifications. The document includes technical specifications, photos, and contact information.
The Automatic Rotary Ropp / Screw Cap Sealing Machine consists of main structure, product transmission belt with adjustable guide, in-feed screw, star plate, sealing heads, vibratory bowl for caps, cap deliver chute, product’s height adjustment screw, safety acrylic cover (OPTIONAL), electrical panel, motor, sensors & AC drive.
Harikrushna Machines Pvt. Ltd. Is a Manufacturers Of Different Type Of Machinery Like Capping Machinery, Single Head Capping Machine To Bottle ROPP Capping Machine, Bottle Screw Capping Machine, Lug Cap Sealing Machines, Dosing Cup Placement Machine, Cap Pressing Machine, Linear Measuring Cup Placement, Vial Capping Machine, Multi-head Vial Capping Machine, Monoblock Plugging And Capping Machine, Lug Capping Machine, Measuring Cup Placement Machine, And High-speed Automatic Pharma Bottle Capping Machine and As Per Customer Requirements.
The Automatic Glass Bottle Sealing Machine consists of main structure, product transmission belt with adjustable guide, in-feed screw, star plate, sealing heads, vibratory bowl for caps, cap deliver chute, product’s height adjustment screw, safety acrylic cover (OPTIONAL), electrical panel, motor, sensors & AC drive.
Harikrushna Machinetech Is A Manufacturer Of Different Type Of Machinery Like Capping Machinery, Single Head Capping Machine To Bottle ROPP Capping Machine, Bottle Screw Capping Machine, Lug Cap Sealing Machines, Dosing Cup Placement Machine, Cap Pressing Machine, Linear Measuring Cup Placement, Vial Capping Machine, Multi-head Vial Capping Machine, Monoblock Plugging, And Capping Machine, Lug Capping Machine, Measuring Cup Placement Machine, And High-speed Automatic Pharma Bottle Capping Machine and As Per Customer Requirements
Automatic Sticker Labeling Machine.
Application:
Used to label small, round shaped products like vials, ampoules, and test tubes.
Features:
Smooth operations
Long service life
Minimum maintenance
HARIKRUSHNA Round BOTTLE LINE Pharma Packaging Line. to the prestigious clients at very inexpensive price.
Other Details:-
Range: 2ml to 30 ml Output Speed: 40 to 150 VPM.
Linear Vial Washing Machine
Premium Filling & Plugging Machine
Premium Sealing Machine
Premium Labelling Machine
Turn Table
This document provides information about a company that manufactures and exports liquid packaging machinery. It describes various machines for washing, filling, capping, labeling, and packaging liquids. The company serves industries such as pharmaceuticals, cosmetics, dairy, food, and more. It has over 10,000 installations worldwide and manufactures machines that meet international certifications. The document includes technical specifications and photos for the different machine types.
This machine is suitable only for plastic vials. It consists of a SS hopper mounted at the top for vial storage. The capacity varies depending upon the size and shape of the vials.
Anny Serafina Love - Letter of Recommendation by Kellen Harkins, MS.AnnySerafinaLove
This letter, written by Kellen Harkins, Course Director at Full Sail University, commends Anny Love's exemplary performance in the Video Sharing Platforms class. It highlights her dedication, willingness to challenge herself, and exceptional skills in production, editing, and marketing across various video platforms like YouTube, TikTok, and Instagram.
Starting a business is like embarking on an unpredictable adventure. It’s a journey filled with highs and lows, victories and defeats. But what if I told you that those setbacks and failures could be the very stepping stones that lead you to fortune? Let’s explore how resilience, adaptability, and strategic thinking can transform adversity into opportunity.
[To download this presentation, visit:
https://www.oeconsulting.com.sg/training-presentations]
This PowerPoint compilation offers a comprehensive overview of 20 leading innovation management frameworks and methodologies, selected for their broad applicability across various industries and organizational contexts. These frameworks are valuable resources for a wide range of users, including business professionals, educators, and consultants.
Each framework is presented with visually engaging diagrams and templates, ensuring the content is both informative and appealing. While this compilation is thorough, please note that the slides are intended as supplementary resources and may not be sufficient for standalone instructional purposes.
This compilation is ideal for anyone looking to enhance their understanding of innovation management and drive meaningful change within their organization. Whether you aim to improve product development processes, enhance customer experiences, or drive digital transformation, these frameworks offer valuable insights and tools to help you achieve your goals.
INCLUDED FRAMEWORKS/MODELS:
1. Stanford’s Design Thinking
2. IDEO’s Human-Centered Design
3. Strategyzer’s Business Model Innovation
4. Lean Startup Methodology
5. Agile Innovation Framework
6. Doblin’s Ten Types of Innovation
7. McKinsey’s Three Horizons of Growth
8. Customer Journey Map
9. Christensen’s Disruptive Innovation Theory
10. Blue Ocean Strategy
11. Strategyn’s Jobs-To-Be-Done (JTBD) Framework with Job Map
12. Design Sprint Framework
13. The Double Diamond
14. Lean Six Sigma DMAIC
15. TRIZ Problem-Solving Framework
16. Edward de Bono’s Six Thinking Hats
17. Stage-Gate Model
18. Toyota’s Six Steps of Kaizen
19. Microsoft’s Digital Transformation Framework
20. Design for Six Sigma (DFSS)
To download this presentation, visit:
https://www.oeconsulting.com.sg/training-presentations
Zodiac Signs and Food Preferences_ What Your Sign Says About Your Tastemy Pandit
Know what your zodiac sign says about your taste in food! Explore how the 12 zodiac signs influence your culinary preferences with insights from MyPandit. Dive into astrology and flavors!
The Genesis of BriansClub.cm Famous Dark WEb PlatformSabaaSudozai
BriansClub.cm, a famous platform on the dark web, has become one of the most infamous carding marketplaces, specializing in the sale of stolen credit card data.
Garments ERP Software in Bangladesh _ Pridesys IT Ltd.pdfPridesys IT Ltd.
Pridesys Garments ERP is one of the leading ERP solution provider, especially for Garments industries which is integrated with
different modules that cover all the aspects of your Garments Business. This solution supports multi-currency and multi-location
based operations. It aims at keeping track of all the activities including receiving an order from buyer, costing of order, resource
planning, procurement of raw materials, production management, inventory management, import-export process, order
reconciliation process etc. It’s also integrated with other modules of Pridesys ERP including finance, accounts, HR, supply-chain etc.
With this automated solution you can easily track your business activities and entire operations of your garments manufacturing
proces
NIMA2024 | De toegevoegde waarde van DEI en ESG in campagnes | Nathalie Lam |...BBPMedia1
Nathalie zal delen hoe DEI en ESG een fundamentele rol kunnen spelen in je merkstrategie en je de juiste aansluiting kan creëren met je doelgroep. Door middel van voorbeelden en simpele handvatten toont ze hoe dit in jouw organisatie toegepast kan worden.
Presentation by Herman Kienhuis (Curiosity VC) on Investing in AI for ABS Alu...Herman Kienhuis
Presentation by Herman Kienhuis (Curiosity VC) on developments in AI, the venture capital investment landscape and Curiosity VC's approach to investing, at the alumni event of Amsterdam Business School (University of Amsterdam) on June 13, 2024 in Amsterdam.
Ellen Burstyn: From Detroit Dreamer to Hollywood Legend | CIO Women MagazineCIOWomenMagazine
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Brian Fitzsimmons on the Business Strategy and Content Flywheel of Barstool S...Neil Horowitz
On episode 272 of the Digital and Social Media Sports Podcast, Neil chatted with Brian Fitzsimmons, Director of Licensing and Business Development for Barstool Sports.
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A select set of project management best practices to keep your project on-track, on-cost and aligned to scope. Many firms have don't have the necessary skills, diligence, methods and oversight of their projects; this leads to slippage, higher costs and longer timeframes. Often firms have a history of projects that simply failed to move the needle. These best practices will help your firm avoid these pitfalls but they require fortitude to apply.
The APCO Geopolitical Radar - Q3 2024 The Global Operating Environment for Bu...APCO
The Radar reflects input from APCO’s teams located around the world. It distils a host of interconnected events and trends into insights to inform operational and strategic decisions. Issues covered in this edition include:
How are Lilac French Bulldogs Beauty Charming the World and Capturing Hearts....Lacey Max
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Discover timeless style with the 2022 Vintage Roman Numerals Men's Ring. Crafted from premium stainless steel, this 6mm wide ring embodies elegance and durability. Perfect as a gift, it seamlessly blends classic Roman numeral detailing with modern sophistication, making it an ideal accessory for any occasion.
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2. OUR MARKET
AUSTRALIA, BANGLADESH, BRAZIL, CHAD, CAMEROON, CANADA,
COLOMBIA, CONGO, EGYPT, ETHIOPIA, FIJI, GHANA, INDIA, INDONESIA,
IRAN, IRAQ, ISRAEL, JORDAN, LATVIA, KENYA, KUWAIT, MALAYSIA,
MEXICO, MONGOLIA, MYANMAR, NEPAL, NIGERIA, PERU, PHILIPPINES,
PORTUGAL, QATAR, ROMANIA, RUSSIA, SAUDI ARABIA, SERBIA, SINGAPORE,
SOUTH AFRICA, SPAIN, SRI LANKA, SYRIA, TANZANIA, TURKEY, U.A.E.,
UGANDA, UKRAINE, U.K., U.S.A., UZBEKISTAN, VENEZUELA, VIETNAM ETC.
www.harikrushna.com 2
“Celebrating Satisfied Installations Worldwide”
10000+
Foot prints at over countries
55
worldwide & still counting.....
3. Message From CMD
“Welcome.... to the trusted & most preferred gateway to knowledge
engineering based innovative packaging solutions”
(a flagship venture of ) one of the most preferred & trusted solution
DAVE'S GROUP OF COMPANIES
provider for primary packaging requirement. We are engaged in manufacturing & exporting of advanced
Liquid processing & packaging machinery for Beverages, Chemicals, Cosmetics, Dairy, Detergents,
Distilleries, Edible Oil Fertilizers, Food, Lubricants Oil, Nutraceuticals, Paints, Pesticides, Pharmaceutical,
Pigments, Plastic. We also offer special purpose machines & material handling equipments.
HMPL has proud patronage of around across globe, which includes major
10000+ installations
segments like Agro-Chemicals & Pesticides, Automobiles, Beverages, Cosmetics, Dairy,
Food, FMCG & Pharmaceuticals to name of few.
Warm Regards,
HARIKRUSHNA Machines Pvt. Ltd.(HMPL) is headquartered at Ahmedabad India, one of the
most preferred business hubs across the globe. We have state of art & advanced
manufacturing unit in Ahmedabad.
We are an ISO 9001-2015 certified organization & the first organization in India to supply
advanced liquid packaging machinary with CE certification.
At , we always endeavor to keep pace with the ever evolving technologies and ensure
HMPL
to offer highly customized packaging solution to industry leaders across the world.
Mr. aulik Dave
M
M
Mr. aulik Dave
M
(Chairman & Managing Director)
Cell : +91 98250 49429
www.harikrushna.com 3
,
HARIKRUSHNA MACHINES PVT. LTD.
4. H T E C
R
OUR CREDENTIALS
OUR ACCOLADES : YOUR TRUST
CMD Receiving prestigious “UDYOG RATTAN AWARD”
by The Gorvernor of Gujarat.
UDYOG RATTAN AWARD
SME EXCELLENCE AWARD
TREND SETTER AWARD
GLOBAL BUSINESS
ACHIEVEMENT AWARD
www.harikrushna.com 4
5. HMPL @ VARIOUS EXHIBITIONS IN INDIA AND GLOBLE
www.harikrushna.com 5
6. PRODUCT INDEX
WASHING SYSTEMS: Page No. 8-11
Rotary Washing Machines
Linear Washing Machines
Air Jet Vacuum Cleaning Machines
Page No. 12-18
FILLING SYSTEMS:
Automatic Volumetric Filling Machines
Premium Filling Machines
Vacuum Filling Machines
Piston Filling Machines
Special Pump Filling Machines
Page No. 19-22
CAPPING SYSTEMS:
Automatic ROPP / Screw Capping Machines
Flip Off / Aluminum Cap Sealing Machines
Induction Cap Sealing Machines
Page No. 23-29
LABELING SYSTEMS:
Automatic Labeling Machines, Premium Labeling Machines, Labeling Machine For Flat Container
Double Side Labeling Machine, Labeling Machine For Round And Flat Container
Labeling Machine For Top Side Labeling, High Speed Labeling Machine For Vials And Ampoules
Labeling Machine For Horizontal Application, Labeling Machine For Liquor Industries
Special Purpose Labeling Machines, General Hologram Applicators
Hologram Applicators For Liquor Industries
Page No. 30-31
COMPOSITE PACKAGING LINE(LIQUID):
Pharmaceutical: Syrup & Suspension Line, Eye & Ear Drops Line, Vial Line, SVP / LVP Packaging Line
FMCG: Cream Line, Hair Oil Line, Shampoo Line, Edible Oil Line, Lube Oil Line
Food / dairy: Honey Line, Juice Line, Milk Line
Pesticides Packaging Line
Liquor Packaging Line
Page No. 32-36
SPECIAL PURPOSE MACHINES:
R&D / F&D Pre-fill Syringe Filling & Stoppering Machines
Semi Automatic Pre-fill Syringe Filling & Stoppering Machines
Fully Automatic Pre-fill Syringe Filling & Stoppering Machines
Automatic Labeling Machine For Pre-fill Syringes
Cartridge Filling & Closing Line
Fully Automatic Shrink Sleeve Applicators
Trio Block (Rinser Filler & Capper)
Cartoning Machine
Tube Filling & Sealing Machine
Page No. 41
ANCILLARIES:
Turn Tables, Roller Conveyors, Packing Conveyors, Bend Conveyors, Slat Conveyors
Inspection Conveyors, Magnifying Glass Conveyors Etc.
www.harikrushna.com 6
7. www.harikrushna.com 7
COSMETICS
PESTICIDES, AGRO & PETRO CHEMICALS
BREWERIES & DISTILLERIES
SPECIAL PURPOSE MACHINES
DAIRY, FOOD & JUICE
REFERRAL CUSTOMERS LIST
“Know us From The People Who Know us”
13. www.harikrushna.com
*subject to customization
SEMI AUTOMATIC TIMER FILLING MACHINE
Useful for water based free flow liquid such as Hair Oil, Lubricants, Shampoo, Spirit,
Edible Oil, Liquid Soap, Ink etc.
FILLING SYSTEMS
SEMI AUTOMATIC / PROTOTYPE SYSTEMS
REFERRAL TECHNICAL SPECIFICATIONS*
10 to 20 bottles (depends on volume & viscosity)
50 ml to 5000 ml
Single Phase / 230V AC / 50Hz
50
www.harikrushna.com 13
14. www.harikrushna.com
*subject to customization
FILLING SYSTEMS
PREMIUM SEMI AUTOMATIC VACUUM FILLING MACHINE
Useful for :
Cosmetic industries- Product container with small mouth like Nail paint, Perfumes etc.
Chemical industries- Solvent based material, Alcohol based material like Phenyl, Wood thinner etc.
Food & Dairy Industries- Butter milk, Fruit Juices etc.
Pharma Industries- Mouth fresheners, Antiseptic liquid etc.
SEMI AUTOMATIC / PROTOTYPE SYSTEMS
REFERRAL TECHNICAL SPECIFICATIONS*
www.harikrushna.com 14
15. www.harikrushna.com
*subject to customization
FILLING SYSTEMS
SEMI AUTOMATIC PERISTALTIC FILLING MACHINE
Useful for Chemical / Acidic material(Phenyl, Bleach, Nail remover etc),
Wax based material (Kajal), High temperature product like Balm.
SEMI AUTOMATIC / PROTOTYPE SYSTEMS
Single Phase / 230V AC / 50Hz
0.1 ml to 1000 ml (Depend on pump capacity)
www.harikrushna.com 15
16. *subject to customization
FILLING SYSTEMS
SEMI AUTOMATIC PISTON FILLING MACHINE
Useful for :
- Food & Dairy Industries (Yoghurt, Butter, Honey & Milk, Butter milk, Lassi, Edibale Oil, Ghee, Jam),
- Cosmetic Industries (Shampoo, Bath care, Lotion Etc.)
- Chemical Industries(Lubricants, Ink, Glue)
SEMI AUTOMATIC / PROTOTYPE SYSTEMS
REFERRAL TECHNICAL SPECIFICATIONS*
www.harikrushna.com 16
17. *subject to customization
FILLING SYSTEMS
AUTOMATIC VOLUMETRIC LIQUID FILLING MACHINE
REFERRAL TECHNICAL SPECIFICATIONS*
HEAD ASSEMBLY
SEMI AUTOMATIC
FILLING SYSYTEM
*Accessories shown may
not be the part of the
standard equipment
Ø The unit is made compact & versatile as
per GMPnorms.
Ø The structure is made of MS cladded
with SS 304.
Ø Rigid vibration free construction for
trouble free performance.
Ø SS elegantly matt finished body.
Ø Drain tray around the machine platform.
Ø Drip tray under the conveyor.
Ø Elegant and easy control panel for total
control on operation.
Ø ± 1 % Filling accuracy on single dose.
Ø Nitrogen purging arrangement
(OPTIONAL).
Ø No bottle No filling system.
Ø Diving nozzle device.
Ø Minimum change overtime, from one
size to another bottle or fill size.
Ø Self-lubricating UHMW-PE guide profile
for SS slat chain provides low friction
wear surface, smooth and noiseless
conveying.
Ø Pneumatic bottle stopping arrangement.
Ø Synchronized two nos. AC drives for
main motor & conveyor belt.
Ø SS measurement scale for filling volume
adjustment.
Ø Safety guard for conveyor gearbox,
motor and pneumatic cylinders.
Ø MCB for over load protection, and
prevent against short circuit.
Ø Inbuilt protection against over current,
voltage fluctuation, short circuit in AC
frequency drive.
10 ml to 500 ml
www.harikrushna.com 17
18. *subject to customization
FILLING SYSTEMS
PREMIUM BOTTLE FILLING MACHINE
REFERRAL TECHNICAL SPECIFICATIONS*
unique change part free
PLC based filling systems
3Phase+Neutral+Earthing / 440V AC / 50Hz
www.harikrushna.com 18
19. *subject to customization
FILLING SYSTEMS
PREMIUM VIAL FILLING AND BUNGING MACHINE
FILLING AREA
BUNGING AREA
*Accessories shown may not be the part of the standard equipment
*
REFERRAL TECHNICAL SPECIFICATIONS
Upto120 VPM
3Phase+Neutral+Earthing/440VAC/50Hz
www.harikrushna.com 19
20. AUTOMATIC ROTARY R.O.P.P / SCREW CAPPING MACHINE
*subject to customization
CAPPING SYSTEMS
SCREW CAP
ROPP CAP
*Accessories shown may not be the part of the standard equipment
Ø The unit is made compact &
versatile as per GMPnorms.
Ø The structure is made of MS
cladded with SS 304.
Ø Rigid vibration free construction
for trouble free performance.
Ø SS Elegantly matt finished body.
Ø No bottle no cap arrangement.
Ø Adjustable height of conveyor belt
to align with other machine of the
line.
Ø Sealing pressure can be varied to
suit different gauges and size of
caps.
Ø No cap in chute vibrator on &
Machine stop.
Ø No bottles Machine Stop.
Ø Clutch overload - Machine
Stop.
Ø Low noise level, low power
consumptions.
Ø Chute will have rigid mounting &
cap pickup arrangement from SS
material.
Ø Mechanical stopper to stop
incoming bottles.
Ø Self-lubricating UHMW- PE guide
profile for low friction wears
surface, smooth and noiseless
conveying.
Ø Star wheel & guide MOC:
UHMW–White.
Ø Adjustable bottle height gauge for
easy and quick setting.
REFERRAL TECHNICAL SPECIFICATIONS*
3Phase+Neutral+Earthing/440VAC/50Hz
www.harikrushna.com 20
21. *subject to customization
CAPPING SYSTEMS
AUTOMATIC PREMIUM BOTTLE CAPPING MACHINE
SCREW CAP
ROPP CAP
REFERRAL TECHNICAL SPECIFICATIONS*
3 Phase+Netural+Earthing / 440V AC / 50Hz
www.harikrushna.com 21
22. *subject to customization
CAPPING SYSTEMS
PREMIUM VIAL CAPPING MACHINE (Aluminum Cap Sealing / Flip off Cap Sealing )
SALIENT FEATURES:
REFERRAL TECHNICAL SPECIFICATIONS*
3Phase+Neutral+Earthing / 440V AC / 50Hz
(with the help of change part)
www.harikrushna.com 22
23. *subject to customization
INDUCTION CAP SEALING MACHINE
SEALING SYSTEMS
MEASURING CUP PLACING MACHINE
HORIZONTAL FLOW WRAPPING MACHINE
www.harikrushna.com 23
24. *subject to customization
PREMIUM SEMI LABELING MACHINE - TABLE TOP MODEL
LABELING SYSTEMS
SEMI AUTOMATIC SYSTEM
REFERRAL TECHNICAL SPECIFICATIONS*
www.harikrushna.com 24
25. *subject to customization
AUTOMATIC SINGLE SIDE VERTICAL LABELING MACHINE
LABELING SYSTEMS
The most preferred labeling machine for round
bottles
The Machine with 21 CFR part 11
“Fixed / variable data printer / 2D-Pharma code
bar code printer, scanner & rejection system
can be synchronized with this machine”
*
REFERRAL TECHNICAL SPECIFICATIONS
SinglePhase/230VAC/ 50Hz
(Incaseof Contact Coder)
www.harikrushna.com 25
26. *subject to customization
PREMIUM LABELING MACHINE
REFERRAL TECHNICAL SPECIFICATIONS*
LABELING SYSTEMS
Upto 120 BPM
SinglePhase/ 230VAC/ 50Hz
(Incaseof Contact Coder)
The Machine with 21 CFR
part 11
“Fixed / variable data printer / 2D-Pharma code
bar code printer, scanner &
rejection system
can be synchronized with this machine”
www.harikrushna.com 26
27. AUTOMATIC SINGLE SIDE VERTICAL LABELING MACHINE
(with in-built Turn Table)
LABELING SYSTEMS
AUTOMATIC SINGLE SIDE VERTICAL LABELING MACHINE (Round & Flat)
The Machine with 21 CFR part 11
“Fixed / variable data printer / 2D-Pharma code
bar code printer, scanner & rejection system
can be synchronized with this machine”
www.harikrushna.com 27
28. LABELING SYSTEMS
AUTOMATIC TOP & SIDE LABELING MACHINE
AUTOMATIC DOUBLE SIDE VERTICAL LABELING MACHINE
AUTOMATIC ROTARY LABELING MACHINE
The Machine with 21 CFR part 11
“Fixed / variable data printer / 2D-Pharma code
bar code printer, scanner & rejection system
can be synchronized with this machine”
www.harikrushna.com 28
29. *subject to customization
LABELING SYSTEMS
AUTOMATIC SINGLE SIDE HORIZONTAL LABELING MACHINE
HOLOGRAM APPLICATOR STAND ALONE UNIT STANDARD
SALIENT FEATURES:
SALIENT FEATURES:
a g p
b p
c
SALIENT FEATURES:
h
t v
t
AUTOMATIC SINGLE SIDE VERTICAL HIGH SPEED
LABELING MACHINE
The Machine with 21 CFR part 11
“Fixed / variable data printer / 2D-Pharma code
bar code printer, scanner & rejection system
can be synchronized with this machine”
www.harikrushna.com 29
32. TRIO BLOCK (RINSER / FILLER / CAPPER)
SPECIAL PURPOSE MACHINES
Ø Structure frame of MS cladded
platform and housings of SS 304.
Ø Rinse fill & seal cycle, fully Trio-
block for total filling hygiene. The
whole process is automatic.
Ø Bottle in-feed using high pressure
air conveyor with air filter on suction
side.
Ø Machine with neck holding system
by design, so few change part
required for different shape of
bottles.
Ø The filling operation is faster and
more stable due to the micro-
pressure filling method.
Ø Electrical control panel mounted.
Ø User friendly acrylic doors.
Ø NO BOTTLE / NO RINSE / NO FILL
/ NO CAP.
Ø Main machine motor with variable
speed &AC drive.
Ø Automatic PLC control speed
regulation.
Ø The advanced PLC is adapted to
c o n t r o l t h e m a c h i n e r u n s
automatically, air conveyor system
is adopted in bottle entry section
and belt conveyor system is
adopted in bottle exit section, which
can adjust speeds and coordinated
with transducer of the main
machine to make the operations of
moving bottle forward steadily and
reliable.
Ø Fully automatic rotor to rotor
transfer without any human
interruption. It is convenient to
operate with higher automation due
to every parts of the machine is
inspected with photo electrical
detector.
Ø Torque adjustable capping heads
using PICK & PLACE provided.
Ø SS 316 material used for filling
valves.
Ø In-feed can be linked directly with
automatic blow moulding machine.
(Optional at extra cost).
Model No. HMPL16-16-5 HMPL18-18-6 HMPL 24-24-8 HMPL32-32-10
Rinsing Head No. 16 18 24 32
Filling head No. 16 18 24 32
Capping head No. 5 6 8 10
Capacity (B/H)
5000 8000 10000 12000
(For 500ml)
Motor Power 3Kw 3Kw 4Kw 4.8Kw
Total Weight Approx. 3.2T 3.6T 4.5T 4.8T
REFERRAL TECHNICAL SPECIFICATIONS
*
Dimension (LXWXH) Approx.
HMPL 16-16-5 2650 X 1850 X 2400 mm
HMPL 18-18-6 2750 X 2050 X 2400 mm
HMPL 24-24-8 3050 X 2250 X 2400 mm
HMPL 32-32-10 3800 X 2800 X 2300 mm
SALIENT FEATURES:
www.harikrushna.com 32
*subject to customization
33. *subject to customization
SPECIAL PURPOSE MACHINES
*
MODEL
Suitable for
Filling station
Output / minute
Dosing accuracy
Power consumption
Power supply
Working heigh
Air consumption
Air supply
Nitrogen supply
HMPL VISCOFILL 20
Viscous substance (1 ml to 3 ml) / aqueous substance
(0.5 ml to 3 ml) with the help of change parts.
1 NO.
20 PFS per minute @ 1ml (Output may vary based on
nature of the filling substance and volume)
+ 1%
2 KW
Three phase / 440V AC / 50Hz (Stabilized)
850mm ± 50mm
5 CFM
6 to 8 Kg / cm²
5 CFM pressure(Customer scope)
*Viscous substance (1 ml to 3 ml) /
aqueous substance (0.5 ml to 3 ml)
accurately with the help of change parts.
PLC
pneumatically
CIP, SIP
www.harikrushna.com 33
34. *subject to customization
SPECIAL PURPOSE MACHINES
PFS FILLING & STOPPERING SYSTEM FOR AQUEOUS DRUGS (0.2ml TO 5ml)
SALIENT FEATURES:
*
REFERRAL TECHNICAL SPECIFICATIONS
MODEL HMPL ACCUFILL 20
Suitable for 0.2 ml to 5 ml*
* WITH THE HELP OF CHANGE PARTS
Filling station 1 NO.
Output / minute 20 PFS @1 ML WITH 1 FILLING STATION (aqueous drug)
Dosing accuracy + 1%
Filling capacity 0.2ml onwards
Power consumption 2 KW
Power supply Three phase, 440V, 50Hz (Stabilized)
Net weight 350 kgs
Working height 850mm ± 50mm
Air consumption 5 CFM
Air supply 6 to 8 Kg / cm²
Nitrogen supply Provide by customer at 5 CFM pressure
CIP / SIP ready system.
Synchronized LAF can be offered at additional cost.
Specialized filling system for aqueous drugs.
www.harikrushna.com 34
36. *subject to customization
REFERRAL TECHNICAL SPECIFICATIONS*
Automatic Sleeve Applicator - Neck:
Ø The unit is made compact & versatile as
per GMPnorms.
Ø Rigid vibration free construction for
trouble free performance.
Ø The SS 304 slat conveyor for proper
product conveying.
Ø In-feed screw for the positive feeding of
bottle (body sleeve) / Belting system for
the positive feeding of bottle (neck
sleeve).
Ø In case roll gets over, there is alarm
notification (buzzer) for indicating the
same.
Ø Web guide control to ensure that there
is no lateral movement of sleeve
laminate.
Ø Separate Stepper Motors for controlling
the movement of rotary brushes to
ensure that sleeve is properly settled on
bottle.
Ø Gaskets, seals and O-rings are
constructed of food grade/ non-toxic
polymeric materials only.
Ø NO BOTTLE NO SLEEVE mechanism.
Ø Unique compact tunnel with minimal
power consumption.
Ø The tunnel comprised of pre and post
heat shrink zone to shrink the sleeve on
bottle.
Ø Overhead convection fan for precise
cooling at output.
Ø Digital temperature controller to ensure
that uniform temperature is maintained
at the time of shrinking.
Ø Sleeve feeding controlled by PLC for
the accurate feeding of sleeve.
Ø Specially designed rotary cutter device
with PLC controlled for cutting of
sleeve.
Ø Emergency stop function on accessible
area.
Ø Total operation of the machine like
speed of conveyor, speed of feeder,
length of sleeve, cutting speed etc. are
controlled by PLC.
Ø Easy to operate PLC by mean of touch
screen HMI.
Ø Most reliable and proven components
such as Festo / SMC make pneumatic
and electric/electronic components
s u c h a s
Panasonic/Bonfiglioli/Motovario make
AC motor, Delta/Allen Bradley makeAC
D r i v e , P L C & H M I , S e n s o r
LEUZE/BANNER/SUNX, MCB & relay
“X” make.
SALIENT FEATURES:
3Phase+Neutral+Earthing / 440V AC / 50Hz
4270mm (L) X 1200mm (W) X 2000mm
www.harikrushna.com 36
37. www.harikrushna.com 37
SALIENT FEATURES
The unit is made compact & versatile as per GMP norms.
The Structure is made of SS 304.
Rigid Vibration free construction for trouble free performance.
The synchronized horizontal pushing system for feeding
the bottles in the machine.
Specially designed adjustable start / stop type bucket conveyor
for conveying the bottles and specially designed chain type start
/ stop feeder conveyor for the cartoons.
Automatic leaflet inserting device with the required no. of folds
(2, 3, 4) and required types (Z type, Q type, parallel type)
-OPTIONAL.
The machine has a facility of no leaflet bottle reject system
(Incase of leaflet inserting). Carton stacker has a facility of
stacking 1000 nos. Cartons.
Facility of no bottles no cartons.
Facility of no cartons machine stop.
Provision of safety interlock of door opening.
Specially Designed vacuum device for pick up of cartonsand
opening of cartons.
No use of vacuum pump to avoid maintenance. Machine has a
specially designed air vacuum generator for the operation of
different assembly such as leaflet pick up and carton pick up.
Adjustable bottle pusher for different size of bottles.
For the various of products, machine has the facility
to chain width.
For the various of products, machine has the facility for
height adjustment by the mean of adjusting screws.
For the various of products, machine has the facility for
length adjustment by the mean of adjusting guide Plate.
Adjustable flaps closing system for side (Top and Bottom)
flap for various size of cartons.
Very less change parts required for change over of the
product. The whole operation is controlled by easy to
operate PLC.
Speed of the machine is synchronized with the PLC
and easy to adjust by mean of HMI.
Product counter facility is inbuilt in the machine to know
the daily production rate.
All the setting parameters with password protection to
avoid any mishandling during machine operation.
Special Kind of HMI mounting panel with 180º rotation
Facility for easy handling of such a 12 feet long machine.
For the initial setting of the machine, it has a JOG
facility itself on HMI.
Any kind of fault will be displayed on touch Screen HMI for
easy understanding for the same.
Machine has online embossing facility for the batch coding
- OPTIONAL.
*subject to customization
up to 200 cartons/minutes.
38. www.harikrushna.com 38
Tube Filling and Sealing Machine
*subject to customization
TECHNICAL SPECIFICATION:
Model HMPL–TFS
Tube Diameter 12 mm Ø to 50 mm Ø (Standard)
Tube Length 50 mm to 200 mm
Filling Capacity 20gms to 250gms Aluminium / LAMI / PVC Tubes
(With the help of required change parts)
Output Speed 20 to 150 Tubes/Minute (Depending on viscosity of material, manual loading)
Power Consumption 2 HP Main Motor / 1 HP Stirrer Motor / 1 KW Jacketed Water Heater (Total 3 KW)
Compressed Air 4 to 5 Bar 100 L/Minute (If have sticky material)
SALIENT FEATURES:
The unit is made compact & Versatile as per GMP Norms.
Ø
Structure is made of MS cladded with SS 304.
Ø
This machine is specially designed to fill, seal and code the
Ø
Aluminium / LAMI / PVC Tubes.
It can be used to fill viscous as well as semi viscous materials
Ø
in LAMI / PVC Tubes.
Machine preset with 20gms to 100gms Piston & Cylinder.
Ø
All the contact parts are made of SS 316 (GMP Model).
Ø
Tube holders are made of nylon for different diameter of tube.
Ø
Relay electrical control systems operating panel with START,
Ø
STOP and INCH.
SENSOR BASE NO TUBE NO FILLS MECHANISM.
Ø
Specially designed hot air sealing unit to seal PVC tubes.
Ø
Motor with variable speed.
Ø
All moving parts are guarded / enclosed.
Ø
Coding Device with 10 letters for one side.
Ø
Hopper temperature thermocouple with digital display.
Ø
40. Next to you,
Before, During and after
the sale in
and around the
INDIA
WORLD
H T E C
R
S
E
C
I
V
R
E
S
E
L
BAILER
www.harikrushna.com 40
41. DOMESTIC / OVERSEAS ASSOCIATE:
Office: Plot No. 513, Phase IV,
G. I. D. C., Vatva, Ahmedabad
382 445, Gujarat (INDIA)
Cell: +91 98250 49429
E-mail: marketing@harikrushna.com
The Only direction for leaders
P
R
O
G
R
E
S
S
www.harikrushna.com 41