This document summarizes a presentation on improving operations performance through electronic guides (eGuides) in regulated industries. It discusses how traditional manufacturing documentation is often paper-based, including standard operating procedures, work orders, and quality records. An eGuide moves this documentation to a digital system, with contents and documents converted to digital files interconnected in a plant operations model. Implementing an eGuide provides benefits like centralized access to documents, version control, electronic signatures, and improved traceability and reporting. The presentation provides examples of how eGuides can model production processes and guide operators through work orders. It also discusses resources for defining, approving, executing, tracking, and analyzing manufacturing operations using eGuides.
Osama EL Sayed Ahmed has over 20 years of experience in dairy and food manufacturing. He holds various roles including Quality Control Manager, Quality Assurance/Control Manager, and Lab & Quality Manager. He has extensive experience developing and implementing quality management systems and food safety programs. He also has expertise in analytical testing, new product development, and customer relations.
The Intertek Quality & Performance Mark is a certification mark that provides third-party validation that a product meets baseline quality and performance levels through independent testing. The mark is designed to help manufacturers and retailers differentiate their products and build consumer trust by demonstrating a product's durability, functionality, lifespan, usability, and workmanship through standardized testing methods. Certification is valid for one year and provides marketing support through product labeling, packaging, displays, and an online listing.
Data analytics to accelerate food product development and innovationinewtrition
Let's start building "Food-as-a-Software" model, where foods are engineered by scientists at a molecular level and uploaded to databases that can be accessed by food designers anywhere in the world. This will result in a far more distributed, localized food-production system that is more stable and resilient than the one it replaces. The new production system will be shielded from volume and price volatility due to the vagaries of seasonality, weather, drought, disease and other natural, economic, and political factors. Geography will no longer offer any competitive advantage. We will move from a centralized system dependent on scarce resources to a distributed system based on abundant resources
Gmp cgmp qa considerations- by Mr. Kailash VilegaveKailash Vilegave
The document discusses good manufacturing practices (GMP) for the pharmaceutical industry. It covers several key points, including that GMP aims to ensure products are consistently manufactured to quality standards, GMP guidelines are established by various international organizations like WHO and FDA, and that GMP compliance involves proper facilities, equipment, documentation, trained personnel, and quality control systems.
I am Seeking an opportunity in gulf area & Egypt , multinational organization
where I can gain practical experience and develop my skills to achieve professional and personal targets.
I have got advanced experiences at QMS ( ISO9001-ISO17025- ISO22000 / HACCP ) and processes establishing, compliance verification and systems auditing
Quality and Food Safety Auditor, GLP, GMP, Hygiene.
. I am14 year Experienced in Quality, HSE, R&D & Manufacturing Operations , Exposure in Multiproduct category i.e Pure natural Mineral water , Juices Beverages,Dairy, Fruit & Vegetable canning, Tomato concentrate processing,
I am Seeking an opportunity in Gulf area & Egypt , multinational organization where I can utilize my experience and my skills to enrich and develop my professional and personal targets."
A Dynamic Professional with over 14 years’ experience in Quality Management, Food Safety & Lab & CHAMICAL & MicrobiologyFOOD, innovation Management, , Cost saving & Supplier Development, Packaging Development, Co- manufacture & Co-Pacer Health and Nutrition, Food Regulations, Crisis Management, Contours improvement and People Management, leadership management, Team work
Expert in Quality Management Systems, GMP, HACCP,ISO 22000, Crisis Management,Risk Assessment,, Innovation, Management, Consumer Complaint, Product & Process Validation & Supplier development & Compliance and Regulatory
Smooth functioning of Microbiology section. Ensure quality of analytical tests performed. Provides technical assistance to market on Microbiology issues
FDA and other governing bodies controlling the standards of medical devices are reaching deeper into the supply chains that support OEMs. As a result, OEMs are now re-evaluating their supplier quality strategies to ensure that every machined component and piece of raw material entering their production floor is 100 percent validated – making quality management a more complex undertaking. Evaluating material suppliers from a risk mitigation standpoint has become a challenging, and somewhat elusive, undertaking for manufacturers of medical devices. The session will answer the questions: What is risk mitigation as it applies to raw material suppliers in the medical device industry? How can orthopaedic device companies combat it?
Raymond Hopkinson has over 20 years of experience in quality assurance roles across various industries including engineering, food processing, chemicals manufacturing, and plastics. He is currently the Quality Systems Lead for an engineering company, where he develops and implements quality plans and inspection test plans to ensure compliance. Previously he held roles as Quality Assurance Coordinator and ISO Auditor for other companies. He has a diploma in Chemical Technology and a degree in Chemistry.
This document summarizes a presentation on improving operations performance through electronic guides (eGuides) in regulated industries. It discusses how traditional manufacturing documentation is often paper-based, including standard operating procedures, work orders, and quality records. An eGuide moves this documentation to a digital system, with contents and documents converted to digital files interconnected in a plant operations model. Implementing an eGuide provides benefits like centralized access to documents, version control, electronic signatures, and improved traceability and reporting. The presentation provides examples of how eGuides can model production processes and guide operators through work orders. It also discusses resources for defining, approving, executing, tracking, and analyzing manufacturing operations using eGuides.
Osama EL Sayed Ahmed has over 20 years of experience in dairy and food manufacturing. He holds various roles including Quality Control Manager, Quality Assurance/Control Manager, and Lab & Quality Manager. He has extensive experience developing and implementing quality management systems and food safety programs. He also has expertise in analytical testing, new product development, and customer relations.
The Intertek Quality & Performance Mark is a certification mark that provides third-party validation that a product meets baseline quality and performance levels through independent testing. The mark is designed to help manufacturers and retailers differentiate their products and build consumer trust by demonstrating a product's durability, functionality, lifespan, usability, and workmanship through standardized testing methods. Certification is valid for one year and provides marketing support through product labeling, packaging, displays, and an online listing.
Data analytics to accelerate food product development and innovationinewtrition
Let's start building "Food-as-a-Software" model, where foods are engineered by scientists at a molecular level and uploaded to databases that can be accessed by food designers anywhere in the world. This will result in a far more distributed, localized food-production system that is more stable and resilient than the one it replaces. The new production system will be shielded from volume and price volatility due to the vagaries of seasonality, weather, drought, disease and other natural, economic, and political factors. Geography will no longer offer any competitive advantage. We will move from a centralized system dependent on scarce resources to a distributed system based on abundant resources
Gmp cgmp qa considerations- by Mr. Kailash VilegaveKailash Vilegave
The document discusses good manufacturing practices (GMP) for the pharmaceutical industry. It covers several key points, including that GMP aims to ensure products are consistently manufactured to quality standards, GMP guidelines are established by various international organizations like WHO and FDA, and that GMP compliance involves proper facilities, equipment, documentation, trained personnel, and quality control systems.
I am Seeking an opportunity in gulf area & Egypt , multinational organization
where I can gain practical experience and develop my skills to achieve professional and personal targets.
I have got advanced experiences at QMS ( ISO9001-ISO17025- ISO22000 / HACCP ) and processes establishing, compliance verification and systems auditing
Quality and Food Safety Auditor, GLP, GMP, Hygiene.
. I am14 year Experienced in Quality, HSE, R&D & Manufacturing Operations , Exposure in Multiproduct category i.e Pure natural Mineral water , Juices Beverages,Dairy, Fruit & Vegetable canning, Tomato concentrate processing,
I am Seeking an opportunity in Gulf area & Egypt , multinational organization where I can utilize my experience and my skills to enrich and develop my professional and personal targets."
A Dynamic Professional with over 14 years’ experience in Quality Management, Food Safety & Lab & CHAMICAL & MicrobiologyFOOD, innovation Management, , Cost saving & Supplier Development, Packaging Development, Co- manufacture & Co-Pacer Health and Nutrition, Food Regulations, Crisis Management, Contours improvement and People Management, leadership management, Team work
Expert in Quality Management Systems, GMP, HACCP,ISO 22000, Crisis Management,Risk Assessment,, Innovation, Management, Consumer Complaint, Product & Process Validation & Supplier development & Compliance and Regulatory
Smooth functioning of Microbiology section. Ensure quality of analytical tests performed. Provides technical assistance to market on Microbiology issues
FDA and other governing bodies controlling the standards of medical devices are reaching deeper into the supply chains that support OEMs. As a result, OEMs are now re-evaluating their supplier quality strategies to ensure that every machined component and piece of raw material entering their production floor is 100 percent validated – making quality management a more complex undertaking. Evaluating material suppliers from a risk mitigation standpoint has become a challenging, and somewhat elusive, undertaking for manufacturers of medical devices. The session will answer the questions: What is risk mitigation as it applies to raw material suppliers in the medical device industry? How can orthopaedic device companies combat it?
Raymond Hopkinson has over 20 years of experience in quality assurance roles across various industries including engineering, food processing, chemicals manufacturing, and plastics. He is currently the Quality Systems Lead for an engineering company, where he develops and implements quality plans and inspection test plans to ensure compliance. Previously he held roles as Quality Assurance Coordinator and ISO Auditor for other companies. He has a diploma in Chemical Technology and a degree in Chemistry.
Catheter Research, Inc. (CRI) is a medical device contract manufacturer and developer specializing in catheters and tubing. It has over 130 employees and was established in 1987. CRI provides cost-effective product development and quality OEM manufacturing services. It has a fully integrated quality system and earned ISO 13485 certification. CRI focuses on lean manufacturing, customer service, and community involvement.
Next-Generation Bioprocessing Monitoring to Enable Smart Data Management and ...MilliporeSigma
Watch this webinar here: https://bit.ly/2ZpV3GU
Biopharmaceutical processes are complex and highly variable in nature. This can result in inconsistent and unpredictable process outcomes. To manage complexity and better understand causes of variability, in-depth knowledge and thorough understanding of the process is critical. Bio4C™ ProcessPad provides the data integration, analysis and sharing across the manufacturing network and end-to-end data management throughout the process lifecycle required for continued process verification, reporting, and analytics.
Bio4C™ ProcessPad is a data visualization, analytics, and process monitoring platform that enables bioprocess lifecycle management, reporting, investigations, and continued process verification (CPV). Intelligently combining process data from batches, Enterprise Resource Planning (ERP), Manufacturing Execution System (MES), Laboratory Information Management System (LIMS), Historian, process equipment, and manual sources into a single, validated data source, Bio4C™ ProcessPad ensures data is current, complete, and contextual throughout the product lifecycle.
In this webinar, you will learn:
• Introduction to Next Generation BioContinuum™ Digital Platform and Bio4C™ Software Suite
• Overview of Bioprocess lifecycle and present biomanufacturing data management challenges
• Introduction to the Bio4C™ ProcessPad digital platform and its modules and features
• Benefits of Bio4C™ ProcessPad in investigations, process monitoring, continued process verification (CPV) and CDMO operations
This document discusses pilot plant scale up in the pharmaceutical industry. It defines a pilot plant as transforming a lab scale formula into a viable product through developing a reliable manufacturing process. Conducting pilot plant studies is important as effects of large scale production cannot be predicted from lab data alone. A pilot plant allows investigating products and processes on an intermediate scale before full production. It permits examining formulas' ability to withstand scale changes and modifying equipment, materials, and production rates. The document outlines pilot plant design, operations including validation, training, engineering support, maintenance, quality assurance, and quality control. The significance of a pilot plant is to refine formulas and determine equipment and materials that can consistently meet specifications for reliable manufacturing.
Ithos Global Best Practices In Supplier Quality And Risk Mgmtkbubeck
This document summarizes a presentation about enhancing supplier quality and risk management at Golden State Foods. It discusses the need to improve vendor management, collect detailed ingredient data, and ensure regulatory compliance when exporting to over 30 countries. The solution implemented was Ithos-Sphere, a platform that provides ingredient archiving, document management, content management, and screening for regulatory compliance. Demo workflows illustrate how to perform tasks like administering users, managing supplier campaigns, conducting advanced searches, and reviewing suppliers. The conclusion encourages learning how similar solutions can boost supplier quality and risk management at other companies.
Pilot Plant Scale Up Techniques Used in Pharmaceutical Manufacturing, Prof. Dr. Basavaraj K. Nanjwade, KLE University College of Pharmacy, Belgaum/Belagavi
Introduction, Objective; Significance; General consideration; Pilot plant scale up technique for solid, liquid and semi solids; SUPAC Guidelies; Introduction to platform technology
validation of blister packaging machineNilesh Utpure
The document discusses validation of packaging machines. It outlines the objectives, importance, and responsibilities of process validation. Validation establishes that a machine meets installation, operational, and performance qualification requirements. The document describes user requirement specifications that cover mandatory parts to guarantee final product quality and compliance. It details the scope, steps in the machine's lifecycle, types of packaging machines, their detailed assembly, key parameters, and the validation SOP.
The document discusses the history and development of copyright law from its origins in the Statute of Anne in 1710 to modern times. It outlines how copyright law has expanded over the centuries to cover new forms of creative works and extend the term of protection. Current US copyright law provides protection for original works fixed in a tangible medium of expression for the life of the author plus 70 years.
Margaret Thatcher became the first female prime minister of the United Kingdom in 1979. She argued for reducing the role of government in the economy and lowering taxes. In 1982, she ordered British troops to defend the Falkland Islands from Argentine invasion. France worked to expand international trade under President Pompidou but economic problems in the 1970s halted renovations of Paris. President Mitterand increased the role of government through nationalizing industries and raising taxes on the wealthy. Arab immigration became a source of tension in France in the 1990s. Germany pursued better relations with communist nations of Eastern Europe under Chancellor Willy Brandt's Ostpolitik policy. The Berlin Wall fell in 1989, ending the division of Germany.
The document describes steps to create a web service in JDeveloper that allows changing passwords for Weblogic users in OBIEE 11g. It then details creating an agent in OBIEE to invoke the web service and a hidden dashboard page for launching the agent to provide a password change functionality accessible from the OBIEE user menu. Configuration changes are also outlined to integrate the password change page into the OBIEE header.
Social Media Workshop at Jordan UniversityDigiArabs
The document provides information about social media platforms and best practices for using them. It discusses major platforms like Facebook, Twitter, LinkedIn and Pinterest. For each platform, it provides key statistics on user numbers and growth. It also offers tips for businesses on how to engage audiences and create effective content for each channel, such as posting at peak hours, using questions to generate discussion, and focusing on stories and visual content for Pinterest.
Zephyr attends a therapy session where he discusses his recent marriage to Liz. The therapist questions whether they truly know each other and communicate well given Zephyr's reluctance to discuss his past trauma. Their session is cut short when Zephyr storms out.
Taz and Dagmar go on a fifth date that ends with them kissing. Taz admits to falling in love with Dagmar, though he seems unsure.
Aerith continues her research at the House of Fallen Leaves but grows bored. Wesley interrupts to talk, though his intentions seem less than pure given his flirtatious remarks toward Aerith.
Masakazu Takasu, Technical Evangelist, TeamLab
http://theconference.se/
Masakazu will show how ingenious technology and art is made in Japan today.
Our next event is MakerFaire trondheim 2014
and ALS Electronica 2014!
http://prix2014.aec.at/prixwinner/13489/
PROTOTYPING EVERYTHING
We grow up exploring ourselves and our surroundings. We learn how to interact with the community we live in. In our early days it’s ok to ask a lot of questions and to learn by doing and failing. Somewhere along the way we become less inclined to play and test to learn how things work, and it seems like we are supposed to know everything about what we do (listen to a politician interviewed on telly). A lot of us forget that craft of testing our way forward.
But, there is a global maker movement that is all about trying things out and building prototypes to understand if an idea works and if there’s a market for it. In this session you will learn about how you can prototype everything from business models to technology.
http://togetter.com/li/708899
The document discusses the views expressed by a speaker in their presentation. It notes repeatedly that these views are those of the speaker and not the organization NAQQAET. It explores various frameworks related to education including Delors' Pillars of learning to know, to do, to live together and to be. It also discusses objectives of business and information technology education such as developing critical thinking skills, preparing students for careers, and graduating future scholars.
The document discusses common student writing problems faced by faculty and potential solutions. It identifies 4 main student problems: 1) poor performance on writing assignments, 2) being unresponsive to assignment instructions, 3) plagiarism and poor use of citations, and 4) not improving from feedback. For each, it lists associated writing issues and challenges faculty may face in addressing them, along with recommended solutions like making instructions explicit, using scaffolds and drafts, and providing targeted feedback.
The Sustainable Living Lab was founded in 2011 as the first makerspace in Singapore. It focuses on social innovation, technology, and sustainability. Since its opening, it has impacted over 15,000 people through various programs like make-a-thons, maker camps, and practicums aimed at helping people discover their skills and talents.
The document discusses an upcoming Singapore Mini Makers Faire on July 25, 2014 where Nick Lewty from the Centre for Quantum Technologies will present on atom-light interaction, experimental setups, optical spectrums, and the Meissner effect in superconductors.
Catheter Research, Inc. (CRI) is a medical device contract manufacturer and developer specializing in catheters and tubing. It has over 130 employees and was established in 1987. CRI provides cost-effective product development and quality OEM manufacturing services. It has a fully integrated quality system and earned ISO 13485 certification. CRI focuses on lean manufacturing, customer service, and community involvement.
Next-Generation Bioprocessing Monitoring to Enable Smart Data Management and ...MilliporeSigma
Watch this webinar here: https://bit.ly/2ZpV3GU
Biopharmaceutical processes are complex and highly variable in nature. This can result in inconsistent and unpredictable process outcomes. To manage complexity and better understand causes of variability, in-depth knowledge and thorough understanding of the process is critical. Bio4C™ ProcessPad provides the data integration, analysis and sharing across the manufacturing network and end-to-end data management throughout the process lifecycle required for continued process verification, reporting, and analytics.
Bio4C™ ProcessPad is a data visualization, analytics, and process monitoring platform that enables bioprocess lifecycle management, reporting, investigations, and continued process verification (CPV). Intelligently combining process data from batches, Enterprise Resource Planning (ERP), Manufacturing Execution System (MES), Laboratory Information Management System (LIMS), Historian, process equipment, and manual sources into a single, validated data source, Bio4C™ ProcessPad ensures data is current, complete, and contextual throughout the product lifecycle.
In this webinar, you will learn:
• Introduction to Next Generation BioContinuum™ Digital Platform and Bio4C™ Software Suite
• Overview of Bioprocess lifecycle and present biomanufacturing data management challenges
• Introduction to the Bio4C™ ProcessPad digital platform and its modules and features
• Benefits of Bio4C™ ProcessPad in investigations, process monitoring, continued process verification (CPV) and CDMO operations
This document discusses pilot plant scale up in the pharmaceutical industry. It defines a pilot plant as transforming a lab scale formula into a viable product through developing a reliable manufacturing process. Conducting pilot plant studies is important as effects of large scale production cannot be predicted from lab data alone. A pilot plant allows investigating products and processes on an intermediate scale before full production. It permits examining formulas' ability to withstand scale changes and modifying equipment, materials, and production rates. The document outlines pilot plant design, operations including validation, training, engineering support, maintenance, quality assurance, and quality control. The significance of a pilot plant is to refine formulas and determine equipment and materials that can consistently meet specifications for reliable manufacturing.
Ithos Global Best Practices In Supplier Quality And Risk Mgmtkbubeck
This document summarizes a presentation about enhancing supplier quality and risk management at Golden State Foods. It discusses the need to improve vendor management, collect detailed ingredient data, and ensure regulatory compliance when exporting to over 30 countries. The solution implemented was Ithos-Sphere, a platform that provides ingredient archiving, document management, content management, and screening for regulatory compliance. Demo workflows illustrate how to perform tasks like administering users, managing supplier campaigns, conducting advanced searches, and reviewing suppliers. The conclusion encourages learning how similar solutions can boost supplier quality and risk management at other companies.
Pilot Plant Scale Up Techniques Used in Pharmaceutical Manufacturing, Prof. Dr. Basavaraj K. Nanjwade, KLE University College of Pharmacy, Belgaum/Belagavi
Introduction, Objective; Significance; General consideration; Pilot plant scale up technique for solid, liquid and semi solids; SUPAC Guidelies; Introduction to platform technology
validation of blister packaging machineNilesh Utpure
The document discusses validation of packaging machines. It outlines the objectives, importance, and responsibilities of process validation. Validation establishes that a machine meets installation, operational, and performance qualification requirements. The document describes user requirement specifications that cover mandatory parts to guarantee final product quality and compliance. It details the scope, steps in the machine's lifecycle, types of packaging machines, their detailed assembly, key parameters, and the validation SOP.
The document discusses the history and development of copyright law from its origins in the Statute of Anne in 1710 to modern times. It outlines how copyright law has expanded over the centuries to cover new forms of creative works and extend the term of protection. Current US copyright law provides protection for original works fixed in a tangible medium of expression for the life of the author plus 70 years.
Margaret Thatcher became the first female prime minister of the United Kingdom in 1979. She argued for reducing the role of government in the economy and lowering taxes. In 1982, she ordered British troops to defend the Falkland Islands from Argentine invasion. France worked to expand international trade under President Pompidou but economic problems in the 1970s halted renovations of Paris. President Mitterand increased the role of government through nationalizing industries and raising taxes on the wealthy. Arab immigration became a source of tension in France in the 1990s. Germany pursued better relations with communist nations of Eastern Europe under Chancellor Willy Brandt's Ostpolitik policy. The Berlin Wall fell in 1989, ending the division of Germany.
The document describes steps to create a web service in JDeveloper that allows changing passwords for Weblogic users in OBIEE 11g. It then details creating an agent in OBIEE to invoke the web service and a hidden dashboard page for launching the agent to provide a password change functionality accessible from the OBIEE user menu. Configuration changes are also outlined to integrate the password change page into the OBIEE header.
Social Media Workshop at Jordan UniversityDigiArabs
The document provides information about social media platforms and best practices for using them. It discusses major platforms like Facebook, Twitter, LinkedIn and Pinterest. For each platform, it provides key statistics on user numbers and growth. It also offers tips for businesses on how to engage audiences and create effective content for each channel, such as posting at peak hours, using questions to generate discussion, and focusing on stories and visual content for Pinterest.
Zephyr attends a therapy session where he discusses his recent marriage to Liz. The therapist questions whether they truly know each other and communicate well given Zephyr's reluctance to discuss his past trauma. Their session is cut short when Zephyr storms out.
Taz and Dagmar go on a fifth date that ends with them kissing. Taz admits to falling in love with Dagmar, though he seems unsure.
Aerith continues her research at the House of Fallen Leaves but grows bored. Wesley interrupts to talk, though his intentions seem less than pure given his flirtatious remarks toward Aerith.
Masakazu Takasu, Technical Evangelist, TeamLab
http://theconference.se/
Masakazu will show how ingenious technology and art is made in Japan today.
Our next event is MakerFaire trondheim 2014
and ALS Electronica 2014!
http://prix2014.aec.at/prixwinner/13489/
PROTOTYPING EVERYTHING
We grow up exploring ourselves and our surroundings. We learn how to interact with the community we live in. In our early days it’s ok to ask a lot of questions and to learn by doing and failing. Somewhere along the way we become less inclined to play and test to learn how things work, and it seems like we are supposed to know everything about what we do (listen to a politician interviewed on telly). A lot of us forget that craft of testing our way forward.
But, there is a global maker movement that is all about trying things out and building prototypes to understand if an idea works and if there’s a market for it. In this session you will learn about how you can prototype everything from business models to technology.
http://togetter.com/li/708899
The document discusses the views expressed by a speaker in their presentation. It notes repeatedly that these views are those of the speaker and not the organization NAQQAET. It explores various frameworks related to education including Delors' Pillars of learning to know, to do, to live together and to be. It also discusses objectives of business and information technology education such as developing critical thinking skills, preparing students for careers, and graduating future scholars.
The document discusses common student writing problems faced by faculty and potential solutions. It identifies 4 main student problems: 1) poor performance on writing assignments, 2) being unresponsive to assignment instructions, 3) plagiarism and poor use of citations, and 4) not improving from feedback. For each, it lists associated writing issues and challenges faculty may face in addressing them, along with recommended solutions like making instructions explicit, using scaffolds and drafts, and providing targeted feedback.
The Sustainable Living Lab was founded in 2011 as the first makerspace in Singapore. It focuses on social innovation, technology, and sustainability. Since its opening, it has impacted over 15,000 people through various programs like make-a-thons, maker camps, and practicums aimed at helping people discover their skills and talents.
The document discusses an upcoming Singapore Mini Makers Faire on July 25, 2014 where Nick Lewty from the Centre for Quantum Technologies will present on atom-light interaction, experimental setups, optical spectrums, and the Meissner effect in superconductors.
Pop art emerged in the 1950s-60s as a reaction to abstract expressionism, using imagery from popular culture like advertisements, comics, and mass-produced objects. Artists like Andy Warhol, Richard Hamilton, Roy Lichtenstein, Claes Oldenburg, and David Hockney employed techniques like silkscreening to critique or celebrate mass media and consumer culture through icons of the everyday. Warhol in particular became famous for his repeated images of Campbell's soup cans and celebrities.
FERRIS WHEEL ILLUSTRATIONS by pupils of 4th grade (Spain)02101954
Ali wakes up early excited for the carnival. He wakes his sister Ayşe who is initially reluctant to get up. They get dressed and have breakfast quickly. On the way there, Ayşe stops to smell flowers and tie her shoes, slowing them down. When they arrive, Ayşe is scared to ride the Ferris wheel but agrees to the bumper cars first. After, she tries to hit a target to win a prize but misses. Ali asks if she's ready for the Ferris wheel now and she keeps her eyes closed during the ride. At the end, Ali suggests the rollercoaster next but Ayşe refuses that ride too.
The document discusses Tata Nano, India's cheapest car. It provides details on its features such as its small size, low price enabled by use of plastics instead of metal, and lack of luxury features to keep costs minimal. The Nano created a new market segment and shattered myths that an inexpensive car can't be safe, spacious or efficient. It generated much controversy during its launch due to protests over its proposed manufacturing plant in West Bengal.
Alliance Semiconductor's clock and timing products include EMI reduction devices, zero delay buffers (ZDB), and frequency multipliers. The portfolio addresses requirements for various applications including PCs, displays, memory modules, consumer devices, networking, and wireless. The products are available in industrial, automotive, and commercial temperature ranges and various package options.
RCM Technologies helped a medical device client implement an electronic medical device reporting (eMDR) system within their existing TrackWise quality management system (QMS). This involved upgrading complaint forms to comply with eMDR standards, configuring TrackWise to allow for electronic submission to the FDA, and validating the new system. The project was completed on time and on budget, reducing costs associated with medical device reporting and ensuring all reports were submitted in compliance with regulations.
The document discusses qualifying critical utilities like HVAC and water systems. It provides an overview of qualification stages including process design, qualification, and continued verification. The presentation emphasizes building quality into systems through a risk-based approach and using tools like Quality by Design, Process Analytical Technology, and corrective action systems. Regulatory guidance recommends understanding processes scientifically and focusing validation on highest risk areas.
This document summarizes a presentation on qualifying critical utilities like HVAC and water systems. It discusses the three stages of process validation according to FDA guidance: process design, process qualification, and continued process verification. It emphasizes building quality into the process from the beginning through understanding risk and science. Utilities and equipment must be qualified before process validation. Monitoring ensures the process remains in control.
Maetrics has over 30 years of experience helping life sciences companies manage regulatory changes and achieve lean compliance. They offer a range of services including regulatory strategies, audits and inspections, quality systems implementation and documentation, validation services, and software tools and training. Maetrics believes in combining lean manufacturing methodologies with industry best practices to solve regulatory, quality, and engineering challenges for their clients.
PAT and QbD concepts in designing the LiMS and other Electronic systems in La...balakrishna t
This document provides an overview of BizBites, a business intelligence and technology solutions provider based in the UK and India since 2004 and 2011 respectively. It also describes tQmlab, one of BizBites' premier management systems for GxP operations and enabling regulatory submissions. tQmlab delivers improved productivity for QA/QC labs through customized workflows for quality control, stability testing, product release testing, and post-release quality testing. It also enables process analytical technology controls in pharmaceutical manufacturing and analytical processes.
The document discusses new product development strategies and processes. It covers identifying opportunities, generating ideas, developing concepts, screening concepts, developing marketing plans, testing products, and commercializing products. Key aspects include establishing cross-functional teams, conducting market research like focus groups, and using stage gates to evaluate concepts and progress new products through the development cycle. The overall process moves from the fuzzy front end of identifying opportunities through developing and launching new products.
The document discusses new product development strategies and processes. It begins by outlining reasons for new product failures, such as overestimating market size. It then describes various NPD strategies including developing original products, acquisitions, and product improvements. The core of the document focuses on the multi-stage NPD process, from opportunity identification and concept development to testing, marketing planning, and commercialization. Cross-functional teams and market research methods like focus groups are also emphasized.
The document discusses strategies for new product development. It outlines the NPD process, including identifying opportunities, generating and screening concepts, developing products, testing concepts and products, and commercializing successful new products. It emphasizes cross-functional collaboration and describes various NPD types, strategies for reducing time to market, and levers for improving the NPD process.
The document discusses new product development strategies and processes. It begins by outlining reasons for new product failures, such as overestimating market size. It then describes various NPD strategies including developing original products, acquisitions, and product improvements. The core of the document focuses on the multi-stage NPD process, from opportunity identification and concept development to testing, marketing planning, and commercialization. Cross-functional teams and market research methods like focus groups are also emphasized.
Quality by Design - Presentation by Naveen PathakWPICPE
This document provides a summary of a presentation on Quality-by-Design (QbD) for biopharmaceuticals. It begins with an overview of QbD and its key principles of product and process understanding and control based on science and risk management. The presentation then discusses applying QbD concepts to coffee making as an example. Key aspects of coffee quality are identified and process parameters that impact quality are described. The presentation emphasizes using process understanding to develop a control strategy to ensure consistent quality. It also discusses integrating QbD with process validation approaches.
This document provides an overview of quality initiatives in the pharmaceutical industry, including the FDA's Pharmaceutical Quality for the 21st Century initiative and quality tools like Six Sigma. It discusses key dimensions of the FDA's initiative like having a risk-based and science-based approach. The document also summarizes pharmaceutical product lifecycles, Process Analytical Technology (PAT), and how approaches like Six Sigma can help drive continuous improvement in quality.
Ricerca Biosciences is a contract development and manufacturing organization located near Cleveland, Ohio on a 43-acre site. It has facilities for process research and development, analytical testing, and cGMP manufacturing. Ricerca has over 300 employees with extensive experience in chemical development. It provides services from drug discovery through commercial manufacturing, with a focus on developing robust, practical processes and ensuring a continuous supply of API. The document describes Ricerca's capabilities and facilities and provides an example project where it improved an early stage process, reducing costs and increasing supply for clinical trials.
PHARMACEUTICAL PROCESS VALIDATION CURRENT REGULATORY ASPECTSMd. Saddam Nawaz
The document discusses pharmaceutical process validation and the lifecycle approach. It provides definitions of process validation from regulatory agencies like the FDA and ICH. The lifecycle approach links product and process development, validation of commercial manufacturing, and continued process verification. It emphasizes understanding sources of variation and controlling variation to consistently deliver quality products. The phases of process validation include process design, process qualification with PPQ batches, and continued process verification. Quality by Design approaches like risk assessment, design of experiments, design space, and control strategy are discussed.
This document discusses process quality management. It examines key elements of process management including research and development, design, management of process quality for all work units and suppliers, systematic quality improvement and quality assessment. It also discusses the history of quality control and various quality control tools and techniques like statistical process control, Pareto analysis, quality function deployment, market research, and the benefits of just-in-time. It emphasizes the importance of controlling processes on a daily basis and moving from inspection to process control through problem solving for continuous improvement.
This document provides an overview of Quality by Design (QbD), including its background and definition. It discusses the FDA's initiative on QbD and why the QbD approach is used. Key quality guidance documents such as ICH Q8, Q8(R1), Q9, and Q10 are summarized. The document compares the current and QbD approaches to pharmaceutical development and provides an example of a QbD approach. It also describes several tools used in QbD like design space, design of experiments, quality risk management, and process analytical technology.
This document discusses strategies for orphan biopharmaceutical process development using contract development and manufacturing organizations (CDMOs). It notes that orphan biopharmaceuticals often require smaller scale and more flexible manufacturing. The document outlines considerations for clinical and commercial process development, including using single-use technologies, quality by design principles, and ensuring fidelity between clinical and commercial manufacturing processes. It emphasizes characterizing processes early and getting the process design right the first time for orphan drugs.
The document provides an overview of quality systems for medical device manufacturers. It discusses the components required by the FDA's Quality System Regulation, including management responsibility, design controls, document controls, purchasing controls, production and process controls, and acceptance activities. It emphasizes that quality systems help ensure consistent compliance with requirements and specifications to improve safety and efficacy.
Customer-led services, independence, confidentiality, integrity, and commitment are the core values of the organization. The organization provides technological assistance and applied research and development services to companies in the food, pharma, chemical and cosmetic sectors. It has over 1,100 associated companies, 200 staff members, and 12,000 square meters of facilities including 7 laboratories and 10 pilot plants.
Quality assurance in the pharmaceutical industryfatboysec
This document discusses quality assurance in the pharmaceutical industry. It states that research, development, production and distribution must comply with global and local rules to ensure medicines are pure, safe and effective. Pharmaceutical companies must satisfy directives from the FDA and EMA regarding GMP, GLP, GCP and GDP. Ordina provides quality assurance services including validation and documentation of processes, training, audit services, and optimization of quality management systems. Ordina experts are knowledgeable in relevant legislation and methodologies to design validation approaches focused on critical quality attributes.
KALYAN CHART SATTA MATKA DPBOSS KALYAN MATKA RESULTS KALYAN MATKA MATKA RESULT KALYAN MATKA TIPS SATTA MATKA MATKA COM MATKA PANA JODI TODAY BATTA SATKA MATKA PATTI JODI NUMBER MATKA RESULTS MATKA CHART MATKA JODI SATTA COM INDIA SATTA MATKA MATKA TIPS MATKA WAPKA ALL MATKA RESULT LIVE ONLINE MATKA RESULT KALYAN MATKA RESULT DPBOSS MATKA 143 MAIN MATKA KALYAN MATKA RESULTS KALYAN CHART
Ellen Burstyn: From Detroit Dreamer to Hollywood Legend | CIO Women MagazineCIOWomenMagazine
In this article, we will dive into the extraordinary life of Ellen Burstyn, where the curtains rise on a story that's far more attractive than any script.
SATTA MATKA DPBOSS KALYAN MATKA RESULTS KALYAN CHART KALYAN MATKA MATKA RESULT KALYAN MATKA TIPS SATTA MATKA MATKA COM MATKA PANA JODI TODAY BATTA SATKA MATKA PATTI JODI NUMBER MATKA RESULTS MATKA CHART MATKA JODI SATTA COM INDIA SATTA MATKA MATKA TIPS MATKA WAPKA ALL MATKA RESULT LIVE ONLINE MATKA RESULT KALYAN MATKA RESULT DPBOSS MATKA 143 MAIN MATKA KALYAN MATKA RESULTS KALYAN CHART INDIA MATKA KALYAN SATTA MATKA 420 INDIAN MATKA SATTA KING MATKA FIX JODI FIX FIX FIX SATTA NAMBAR MATKA INDIA SATTA BATTA
During the budget session of 2024-25, the finance minister, Nirmala Sitharaman, introduced the “solar Rooftop scheme,” also known as “PM Surya Ghar Muft Bijli Yojana.” It is a subsidy offered to those who wish to put up solar panels in their homes using domestic power systems. Additionally, adopting photovoltaic technology at home allows you to lower your monthly electricity expenses. Today in this blog we will talk all about what is the PM Surya Ghar Muft Bijli Yojana. How does it work? Who is eligible for this yojana and all the other things related to this scheme?
SATTA MATKA DPBOSS KALYAN MATKA RESULTS KALYAN MATKA MATKA RESULT KALYAN MATKA TIPS SATTA MATKA MATKA COM MATKA PANA JODI TODAY BATTA SATKA MATKA PATTI JODI NUMBER MATKA RESULTS MATKA CHART MATKA JODI SATTA COM INDIA SATTA MATKA MATKA TIPS MATKA WAPKA ALL MATKA RESULT LIVE ONLINE MATKA RESULT KALYAN MATKA RESULT DPBOSS MATKA 143 MAIN MATKA KALYAN MATKA RESULTS KALYAN CHART KALYAN CHART
The Steadfast and Reliable Bull: Taurus Zodiac Signmy Pandit
Explore the steadfast and reliable nature of the Taurus Zodiac Sign. Discover the personality traits, key dates, and horoscope insights that define the determined and practical Taurus, and learn how their grounded nature makes them the anchor of the zodiac.
DPBOSS NET SPBOSS SATTA MATKA RESULT KALYAN MATKA GUESSING FREE KALYAN FIX JO...essorprof62
DPBOSS NET SPBOSS SATTA MATKA RESULT KALYAN MATKA GUESSING FREE KALYAN FIX JODI ANK LEAK FIX GAME BY DP BOSS MATKA SATTA NUMBER TODAY LUCKY NUMBER FREE TIPS ...
SATTA MATKA DPBOSS KALYAN MATKA RESULTS KALYAN CHART KALYAN MATKA MATKA RESULT KALYAN MATKA TIPS SATTA MATKA MATKA COM MATKA PANA JODI TODAY BATTA SATKA MATKA PATTI JODI NUMBER MATKA RESULTS MATKA CHART MATKA JODI SATTA COM INDIA SATTA MATKA MATKA TIPS MATKA WAPKA ALL MATKA RESULT LIVE ONLINE MATKA RESULT KALYAN MATKA RESULT DPBOSS MATKA 143 MAIN MATKA KALYAN MATKA RESULTS KALYAN CHART
SATTA MATKA DPBOSS KALYAN MATKA RESULTS KALYAN CHART KALYAN MATKA MATKA RESULT KALYAN MATKA TIPS SATTA MATKA MATKA COM MATKA PANA JODI TODAY BATTA SATKA MATKA PATTI JODI NUMBER MATKA RESULTS MATKA CHART MATKA JODI SATTA COM INDIA SATTA MATKA MATKA TIPS MATKA WAPKA ALL MATKA RESULT LIVE ONLINE MATKA RESULT KALYAN MATKA RESULT DPBOSS MATKA 143 MAIN MATKA KALYAN MATKA RESULTS KALYAN CHART
7. Restaurant
Operations
Restaurants Cost Reduction
Performance
Optimization
Food Safety / Quality
Control System Risk
IT
Industry Assessment, Manufacturing (MES) IT
Systems
Selection &
Visionaries Integration Supply Chain
Management
Business Process
Consulting
Executive Business Analytics
Activity Based
Costing
8. Industry Visionaries
• Product Commercialization
• Operations GAP Assessment
Restaurants • Equipment Effectiveness Assessment
• Operations KPI Development
• Quality Systems
9. Industry Visionaries
Real-Time Manufacturing (Operations) Performance
Management™ (RTMPM)
Manufacturing Consulting
• Lean Six Sigma Manufacturing
• PROCAM™ Manufacturing Process Cost Analysis at SKU Level
• Lean Logistics
• Kanban & Flow Technology
• ISA S88 & S95 Standards Compliance
IT • Supply Chain Operations Simulation Modeling
Assessment, • KPI Reporting
System Integrations
Selection & • MES (Manufacturing Execution Systems) Plant-to-ERP
• Finite Capacity Planning & Scheduling
Integration • Plant Automation
• Supply Chain Management
• QSR/Retail Grocery/C-Store Bar Code Food Tracking
Independent Assessments
• Demand Planning
• Supply Planning
• Plant Maintenance Management “GAP Assessments”
• MES “GAP Assessments”
10. Industry Visionaries
• Business Process Management & Mapping
• R&D/Marketing Strategy Synchronization
Executive • Seminars & Workshops
− Food Innovation Processes
− Manufacturing Systems
− Supply Chain Strategy
− KPI Development
16. New Product
Innovation
International Marketing Consulting
Technical Consulting
Training
Product & Education
Seminars &
Workshops
Process Organic Certification
Experts Recalls
Expertise Crisis Management
Legal Expert Witness
Consulting
17. Product & Process Experts
• International Supply Chain Development
• Sales & Marketing
• “Target Customer” Sales Strategies
International • “Micro-Marketing™” Strategies for New Products
• Country of Origin Food Plant Audit Certification
• U.S. COOL Labeling Facilitation
• New Restaurant Food Sourcing
18. Product & Process Experts
• Innovation Workshops
• Batter & Breading Workshops
• Manufacturing IT Systems Selected Topics
Education • Green Sustainability
• Supply Chain Management Systems
• HACCP Programs
• Global Food Safety Initiative