FBIF2015 is taking place on 13th – 15th May, 2015 in Shanghai, we are looking forward to your participation, please pay attention to our site for the latest event info.
Key Considerations & Case Study for Building a cGMP Biomanufacturing FacilityMilliporeSigma
Every biopharma executive must make important decisions early in clinical development. One of these decisions includes defining the commercial manufacturing strategy for their biopharmaceutical and whether it makes business sense to build their own cGMP biomanufacturing facility. We have gained significant expertise throughout the design, build and ongoing operations of the Biodevelopment Center in Martillac, France that could prove invaluable to companies that are considering whether to build their own cGMP facility or outsource to a contract manufacturing organization. In this webinar, our experts share some key considerations for designing, building and operating an agile and flexible cGMP biomanufacturing facility successfully, safely, and profitably.
In this webinar, you will learn:
- How to design and build a flexible and agile facility
- The regulatory requirements for the facility
- How we have converted a stainless steel cGMP bioproduction facility in Martillac, France into a state-of-the-art, fully single-use cGMP facility
Beyond Bioprocessing 4.0: The Convergence of IT, OT and Processing Technolog...Merck Life Sciences
Watch the interactive on-demand webinar here: https://bit.ly/2G8KSMu
The cost to develop and manufacture monoclonal antibodies has been highlighted as a substantial hurdle towards the widespread availability of these effective therapies for patients. Facility costs, utilization and labor are key contributing factors to the overall cost of these critical medicines. A proven method to increase utilization of a facility, increase process and quality robustness and lower overall costs of manufacturing is through the automation of a manufacturing process. The transformative impact that digital technologies have had on other industries’ manufacturing operations through IT and OT can be applied to the evolution happening in biopharma today. Examples of commonly used unit operations such as bioreactor, mixing and chromatography will be presented to illustrate incremental improvements that can be achieved today, and what the future looks like with the convergence of Operational Technology (OT), Information Technology (IT) and existing processing technologies.
In this webinar, you will learn:
- Incremental improvements that can be achieved today using process automation
- Practical examples of commonly used operations to illustrate the impact of automation
- How the automated facility will look like in the future
FBIF2015 is taking place on 13th – 15th May, 2015 in Shanghai, we are looking forward to your participation, please pay attention to our site for the latest event info.
Key Considerations & Case Study for Building a cGMP Biomanufacturing FacilityMilliporeSigma
Every biopharma executive must make important decisions early in clinical development. One of these decisions includes defining the commercial manufacturing strategy for their biopharmaceutical and whether it makes business sense to build their own cGMP biomanufacturing facility. We have gained significant expertise throughout the design, build and ongoing operations of the Biodevelopment Center in Martillac, France that could prove invaluable to companies that are considering whether to build their own cGMP facility or outsource to a contract manufacturing organization. In this webinar, our experts share some key considerations for designing, building and operating an agile and flexible cGMP biomanufacturing facility successfully, safely, and profitably.
In this webinar, you will learn:
- How to design and build a flexible and agile facility
- The regulatory requirements for the facility
- How we have converted a stainless steel cGMP bioproduction facility in Martillac, France into a state-of-the-art, fully single-use cGMP facility
Beyond Bioprocessing 4.0: The Convergence of IT, OT and Processing Technolog...Merck Life Sciences
Watch the interactive on-demand webinar here: https://bit.ly/2G8KSMu
The cost to develop and manufacture monoclonal antibodies has been highlighted as a substantial hurdle towards the widespread availability of these effective therapies for patients. Facility costs, utilization and labor are key contributing factors to the overall cost of these critical medicines. A proven method to increase utilization of a facility, increase process and quality robustness and lower overall costs of manufacturing is through the automation of a manufacturing process. The transformative impact that digital technologies have had on other industries’ manufacturing operations through IT and OT can be applied to the evolution happening in biopharma today. Examples of commonly used unit operations such as bioreactor, mixing and chromatography will be presented to illustrate incremental improvements that can be achieved today, and what the future looks like with the convergence of Operational Technology (OT), Information Technology (IT) and existing processing technologies.
In this webinar, you will learn:
- Incremental improvements that can be achieved today using process automation
- Practical examples of commonly used operations to illustrate the impact of automation
- How the automated facility will look like in the future
Conheça e veja porque que a VersaFlex é a líder Mundial na tecnologia de poliureia. Conheça a equipe, as instalações, os processos, certificados. VersaFlex a empresa que orgulhosamente representamos com exclusividade no Brasil.
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?
Colder Products Company-Aseptic Connections for Single Use ApplicationsLynzee Perdaris
Single Use Technology Integration with Aseptic Connections to Meet Sterility, Dependability, Quality and Traceability! For more information contact Lynzee Perdaris at lperdaris@stiflow.com.
Quality System Expectations : Single-Use Materialsgueste42f6b5
Single-Use technologies supply materials to the biomanufacturing process that replace the need for stainless steel and traditional manufacturing processes which require extensive validation and process development.
Dry ice cleaning for foundry catalog cold jetCold Jet Polska
W Odlewnictwie jednym z problemów są przestoje spowodowane czyszczeniem stałych form aluminiowych, kanałów odpowietrzeń, rdzennic i maszyn odlewniczych. Tradycyjne formy czyszczenia wymagają schłodzenia, demontażu urządzeń, wielu bezproduktywnych godzin czyszczenia i ponownego ich złożenia.
Czyszczenie suchym lodem skraca czas czyszczenia o 60% oraz eliminuje uszkodzenia sprzętu i powstawanie odpadów produkcyjnych. Pozwala czyścić on-line w temperaturze roboczej i nie wymaga demontażu maszyn!
A major issue for the foundry and forging industries is the downtime caused when cleaning permanent aluminum molds, core box vents, semi-solid castings and die casting machines. Typical manual cleaning methods require cool down, disassembly, unproductive hours of messy hand cleaning or bead blast cleaning and then reassembly. In addition, most traditional cleaning methods are not fully effective and often result in damage to the part or equipment.
Dry ice cleaning offers significant improvement in cleaning times (up to 60%) as well as reduction of damage to equipment and resulting scrap product. Dry ice blast cleaning is a non-conductive, in-place method to clean parts and even touch-up cleaning is safe and easy.
009 what are the systems validation protocol methods at atl 05 28-2015atlmarketing
If your product must meet the requirements of FDA cGMP, 21 CFR 210, 211, 820, ISO-9000, ISO-13485, or MDD/93/42/EEC (for the CE Mark), there are three very critical elements you must have to be in regulatory compliance. First, you must have a sound and strong Quality Management System (QMS). This is an expression of WHAT you do (your quality policies and structure). Second, you must have reliable Standard Operating Procedures (SOP’s). These are expressions of HOW YOU DO THINGS.
Missing in the above two items is an expression of HOW WELL YOU DO WHAT YOU DO? This is where you must establish your “Systems Validation Protocol” (SVP). Your SVP is an expression of how well your system is working (for example, this can be expressed in overall product conformance percentage or in defects per million for your various products). The SVP is a living and continuous document based on your quality records. The ATL White Paper “What Are The Systems Validation Protocol Methods At ATL?” is our attempt to share with you a sound approach to Systems Validation and the various protocols that you can use.
Automated Packaging Systems, Inc. has been a world leader in designing and manufacturing flexible bag packaging systems since 1962. We are the original inventor of Autobag® bagging machines and pre-opened bags.
In addition to genuine Autobag bags-on-a-roll, we manufacture SidePouch® specialty bags, AirPouch® void-fill pillows and protective packaging, AutoSleeve Stretch Sleeve labels and a variety of bag packaging equipment.
ALT Technologies company presentation d1m07y21v01 carlosBeata Linz (Kis)
ALT Technologies is your cutting-edge solutions partner for occupant safety components, custom-made labels, RFID labels, EMI shielding, as well as thermal, protective and functional parts.
Our solutions accelerate your success.
Conheça e veja porque que a VersaFlex é a líder Mundial na tecnologia de poliureia. Conheça a equipe, as instalações, os processos, certificados. VersaFlex a empresa que orgulhosamente representamos com exclusividade no Brasil.
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?
Colder Products Company-Aseptic Connections for Single Use ApplicationsLynzee Perdaris
Single Use Technology Integration with Aseptic Connections to Meet Sterility, Dependability, Quality and Traceability! For more information contact Lynzee Perdaris at lperdaris@stiflow.com.
Quality System Expectations : Single-Use Materialsgueste42f6b5
Single-Use technologies supply materials to the biomanufacturing process that replace the need for stainless steel and traditional manufacturing processes which require extensive validation and process development.
Dry ice cleaning for foundry catalog cold jetCold Jet Polska
W Odlewnictwie jednym z problemów są przestoje spowodowane czyszczeniem stałych form aluminiowych, kanałów odpowietrzeń, rdzennic i maszyn odlewniczych. Tradycyjne formy czyszczenia wymagają schłodzenia, demontażu urządzeń, wielu bezproduktywnych godzin czyszczenia i ponownego ich złożenia.
Czyszczenie suchym lodem skraca czas czyszczenia o 60% oraz eliminuje uszkodzenia sprzętu i powstawanie odpadów produkcyjnych. Pozwala czyścić on-line w temperaturze roboczej i nie wymaga demontażu maszyn!
A major issue for the foundry and forging industries is the downtime caused when cleaning permanent aluminum molds, core box vents, semi-solid castings and die casting machines. Typical manual cleaning methods require cool down, disassembly, unproductive hours of messy hand cleaning or bead blast cleaning and then reassembly. In addition, most traditional cleaning methods are not fully effective and often result in damage to the part or equipment.
Dry ice cleaning offers significant improvement in cleaning times (up to 60%) as well as reduction of damage to equipment and resulting scrap product. Dry ice blast cleaning is a non-conductive, in-place method to clean parts and even touch-up cleaning is safe and easy.
009 what are the systems validation protocol methods at atl 05 28-2015atlmarketing
If your product must meet the requirements of FDA cGMP, 21 CFR 210, 211, 820, ISO-9000, ISO-13485, or MDD/93/42/EEC (for the CE Mark), there are three very critical elements you must have to be in regulatory compliance. First, you must have a sound and strong Quality Management System (QMS). This is an expression of WHAT you do (your quality policies and structure). Second, you must have reliable Standard Operating Procedures (SOP’s). These are expressions of HOW YOU DO THINGS.
Missing in the above two items is an expression of HOW WELL YOU DO WHAT YOU DO? This is where you must establish your “Systems Validation Protocol” (SVP). Your SVP is an expression of how well your system is working (for example, this can be expressed in overall product conformance percentage or in defects per million for your various products). The SVP is a living and continuous document based on your quality records. The ATL White Paper “What Are The Systems Validation Protocol Methods At ATL?” is our attempt to share with you a sound approach to Systems Validation and the various protocols that you can use.
Automated Packaging Systems, Inc. has been a world leader in designing and manufacturing flexible bag packaging systems since 1962. We are the original inventor of Autobag® bagging machines and pre-opened bags.
In addition to genuine Autobag bags-on-a-roll, we manufacture SidePouch® specialty bags, AirPouch® void-fill pillows and protective packaging, AutoSleeve Stretch Sleeve labels and a variety of bag packaging equipment.
ALT Technologies company presentation d1m07y21v01 carlosBeata Linz (Kis)
ALT Technologies is your cutting-edge solutions partner for occupant safety components, custom-made labels, RFID labels, EMI shielding, as well as thermal, protective and functional parts.
Our solutions accelerate your success.
This presentation discusses the laboratory test method UN Manual of Tests and Criteria, Part III, Section 37.1 - Corrosion to Metals.
Dell Tech is an ISO 17025 accredited laboratory that can test your product for corrosion to metals. Contact Dell Tech today to schedule testing for your product.
AS A LEADING-EDGE INDUSTRIAL INTEGRATOR,
BOCCARD DESIGNS AND BUILDS UNIQUE
PHARMACEUTICAL AND BIOTECHNOLOGY
LABORATORIES THAT FACILITATE THE PRODUCTION
OF ALL LIQUIDS AND SEMI-LIQUID
FORMS, GELS AND CREAMS. BOCCARD IS THE
INDUSTRIAL INTEGRATOR THAT BRINGS YOUR
PROJECTS TO LIFE – ON TIME AND ON BUDGET
Innovations in Energy Efficiency
Energy Efficiency by Design
Only those who use energy will be successful in the long
run.
Whether in energy distribution, automation, building
services or IT infrastructure – there is savings potential
waiting to be uncovered in every corner of a company.
But it will likely go unnoticed without close scrutiny of the
overarching processes and correlations.Energy Efficiency by Design
Rittal offers integrated solutions with tangible savings
potential, from analysis and planning through to
implementation.
All from a single source – that is what we mean by
RITTAL – THE SYSTEM
Similar to CDF Cheertainer Bag-in-Box Flexible Packaging (20)
Overview of rigid containers- ranges and styles, filling equipment, considerations when filling rigid containers and Flexible filling review- types of flexible packaging, types of filling equipment, considerations when selecting flexible packaging, considerations when selecting filling equipment
History of drum liners, benefits of using drum liners, break down of typical drum liner markets, styles of drum liners, typical liner manufacturing processes.
The Cheer Pack pouch features an easy-flow straw with a reclosable, tamper-evident, screw-on top. The pouch is made from a multi-layer laminate material, with 3-4 layers in a standard configuration. An outer layer of glossy polyester is used to protect our high quality Rotogravure printing. The next layer is selected based on the barrier properties required. An additional layer of nylon is added to increase the strength properties of larger package formats. The internal or final layer is a polyethylene or polypropelene sealing layer.
"𝑩𝑬𝑮𝑼𝑵 𝑾𝑰𝑻𝑯 𝑻𝑱 𝑰𝑺 𝑯𝑨𝑳𝑭 𝑫𝑶𝑵𝑬"
𝐓𝐉 𝐂𝐨𝐦𝐬 (𝐓𝐉 𝐂𝐨𝐦𝐦𝐮𝐧𝐢𝐜𝐚𝐭𝐢𝐨𝐧𝐬) is a professional event agency that includes experts in the event-organizing market in Vietnam, Korea, and ASEAN countries. We provide unlimited types of events from Music concerts, Fan meetings, and Culture festivals to Corporate events, Internal company events, Golf tournaments, MICE events, and Exhibitions.
𝐓𝐉 𝐂𝐨𝐦𝐬 provides unlimited package services including such as Event organizing, Event planning, Event production, Manpower, PR marketing, Design 2D/3D, VIP protocols, Interpreter agency, etc.
Sports events - Golf competitions/billiards competitions/company sports events: dynamic and challenging
⭐ 𝐅𝐞𝐚𝐭𝐮𝐫𝐞𝐝 𝐩𝐫𝐨𝐣𝐞𝐜𝐭𝐬:
➢ 2024 BAEKHYUN [Lonsdaleite] IN HO CHI MINH
➢ SUPER JUNIOR-L.S.S. THE SHOW : Th3ee Guys in HO CHI MINH
➢FreenBecky 1st Fan Meeting in Vietnam
➢CHILDREN ART EXHIBITION 2024: BEYOND BARRIERS
➢ WOW K-Music Festival 2023
➢ Winner [CROSS] Tour in HCM
➢ Super Show 9 in HCM with Super Junior
➢ HCMC - Gyeongsangbuk-do Culture and Tourism Festival
➢ Korean Vietnam Partnership - Fair with LG
➢ Korean President visits Samsung Electronics R&D Center
➢ Vietnam Food Expo with Lotte Wellfood
"𝐄𝐯𝐞𝐫𝐲 𝐞𝐯𝐞𝐧𝐭 𝐢𝐬 𝐚 𝐬𝐭𝐨𝐫𝐲, 𝐚 𝐬𝐩𝐞𝐜𝐢𝐚𝐥 𝐣𝐨𝐮𝐫𝐧𝐞𝐲. 𝐖𝐞 𝐚𝐥𝐰𝐚𝐲𝐬 𝐛𝐞𝐥𝐢𝐞𝐯𝐞 𝐭𝐡𝐚𝐭 𝐬𝐡𝐨𝐫𝐭𝐥𝐲 𝐲𝐨𝐮 𝐰𝐢𝐥𝐥 𝐛𝐞 𝐚 𝐩𝐚𝐫𝐭 𝐨𝐟 𝐨𝐮𝐫 𝐬𝐭𝐨𝐫𝐢𝐞𝐬."
Attending a job Interview for B1 and B2 Englsih learnersErika906060
It is a sample of an interview for a business english class for pre-intermediate and intermediate english students with emphasis on the speking ability.
Business Valuation Principles for EntrepreneursBen Wann
This insightful presentation is designed to equip entrepreneurs with the essential knowledge and tools needed to accurately value their businesses. Understanding business valuation is crucial for making informed decisions, whether you're seeking investment, planning to sell, or simply want to gauge your company's worth.
Personal Brand Statement:
As an Army veteran dedicated to lifelong learning, I bring a disciplined, strategic mindset to my pursuits. I am constantly expanding my knowledge to innovate and lead effectively. My journey is driven by a commitment to excellence, and to make a meaningful impact in the world.
[Note: This is a partial preview. To download this presentation, visit:
https://www.oeconsulting.com.sg/training-presentations]
Sustainability has become an increasingly critical topic as the world recognizes the need to protect our planet and its resources for future generations. Sustainability means meeting our current needs without compromising the ability of future generations to meet theirs. It involves long-term planning and consideration of the consequences of our actions. The goal is to create strategies that ensure the long-term viability of People, Planet, and Profit.
Leading companies such as Nike, Toyota, and Siemens are prioritizing sustainable innovation in their business models, setting an example for others to follow. In this Sustainability training presentation, you will learn key concepts, principles, and practices of sustainability applicable across industries. This training aims to create awareness and educate employees, senior executives, consultants, and other key stakeholders, including investors, policymakers, and supply chain partners, on the importance and implementation of sustainability.
LEARNING OBJECTIVES
1. Develop a comprehensive understanding of the fundamental principles and concepts that form the foundation of sustainability within corporate environments.
2. Explore the sustainability implementation model, focusing on effective measures and reporting strategies to track and communicate sustainability efforts.
3. Identify and define best practices and critical success factors essential for achieving sustainability goals within organizations.
CONTENTS
1. Introduction and Key Concepts of Sustainability
2. Principles and Practices of Sustainability
3. Measures and Reporting in Sustainability
4. Sustainability Implementation & Best Practices
To download the complete presentation, visit: https://www.oeconsulting.com.sg/training-presentations
LA HUG - Video Testimonials with Chynna Morgan - June 2024Lital Barkan
Have you ever heard that user-generated content or video testimonials can take your brand to the next level? We will explore how you can effectively use video testimonials to leverage and boost your sales, content strategy, and increase your CRM data.🤯
We will dig deeper into:
1. How to capture video testimonials that convert from your audience 🎥
2. How to leverage your testimonials to boost your sales 💲
3. How you can capture more CRM data to understand your audience better through video testimonials. 📊
RMD24 | Debunking the non-endemic revenue myth Marvin Vacquier Droop | First ...BBPMedia1
Marvin neemt je in deze presentatie mee in de voordelen van non-endemic advertising op retail media netwerken. Hij brengt ook de uitdagingen in beeld die de markt op dit moment heeft op het gebied van retail media voor niet-leveranciers.
Retail media wordt gezien als het nieuwe advertising-medium en ook mediabureaus richten massaal retail media-afdelingen op. Merken die niet in de betreffende winkel liggen staan ook nog niet in de rij om op de retail media netwerken te adverteren. Marvin belicht de uitdagingen die er zijn om echt aansluiting te vinden op die markt van non-endemic advertising.
Enterprise Excellence is Inclusive Excellence.pdfKaiNexus
Enterprise excellence and inclusive excellence are closely linked, and real-world challenges have shown that both are essential to the success of any organization. To achieve enterprise excellence, organizations must focus on improving their operations and processes while creating an inclusive environment that engages everyone. In this interactive session, the facilitator will highlight commonly established business practices and how they limit our ability to engage everyone every day. More importantly, though, participants will likely gain increased awareness of what we can do differently to maximize enterprise excellence through deliberate inclusion.
What is Enterprise Excellence?
Enterprise Excellence is a holistic approach that's aimed at achieving world-class performance across all aspects of the organization.
What might I learn?
A way to engage all in creating Inclusive Excellence. Lessons from the US military and their parallels to the story of Harry Potter. How belt systems and CI teams can destroy inclusive practices. How leadership language invites people to the party. There are three things leaders can do to engage everyone every day: maximizing psychological safety to create environments where folks learn, contribute, and challenge the status quo.
Who might benefit? Anyone and everyone leading folks from the shop floor to top floor.
Dr. William Harvey is a seasoned Operations Leader with extensive experience in chemical processing, manufacturing, and operations management. At Michelman, he currently oversees multiple sites, leading teams in strategic planning and coaching/practicing continuous improvement. William is set to start his eighth year of teaching at the University of Cincinnati where he teaches marketing, finance, and management. William holds various certifications in change management, quality, leadership, operational excellence, team building, and DiSC, among others.
Affordable Stationery Printing Services in Jaipur | Navpack n PrintNavpack & Print
Looking for professional printing services in Jaipur? Navpack n Print offers high-quality and affordable stationery printing for all your business needs. Stand out with custom stationery designs and fast turnaround times. Contact us today for a quote!
Memorandum Of Association Constitution of Company.pptseri bangash
www.seribangash.com
A Memorandum of Association (MOA) is a legal document that outlines the fundamental principles and objectives upon which a company operates. It serves as the company's charter or constitution and defines the scope of its activities. Here's a detailed note on the MOA:
Contents of Memorandum of Association:
Name Clause: This clause states the name of the company, which should end with words like "Limited" or "Ltd." for a public limited company and "Private Limited" or "Pvt. Ltd." for a private limited company.
https://seribangash.com/article-of-association-is-legal-doc-of-company/
Registered Office Clause: It specifies the location where the company's registered office is situated. This office is where all official communications and notices are sent.
Objective Clause: This clause delineates the main objectives for which the company is formed. It's important to define these objectives clearly, as the company cannot undertake activities beyond those mentioned in this clause.
www.seribangash.com
Liability Clause: It outlines the extent of liability of the company's members. In the case of companies limited by shares, the liability of members is limited to the amount unpaid on their shares. For companies limited by guarantee, members' liability is limited to the amount they undertake to contribute if the company is wound up.
https://seribangash.com/promotors-is-person-conceived-formation-company/
Capital Clause: This clause specifies the authorized capital of the company, i.e., the maximum amount of share capital the company is authorized to issue. It also mentions the division of this capital into shares and their respective nominal value.
Association Clause: It simply states that the subscribers wish to form a company and agree to become members of it, in accordance with the terms of the MOA.
Importance of Memorandum of Association:
Legal Requirement: The MOA is a legal requirement for the formation of a company. It must be filed with the Registrar of Companies during the incorporation process.
Constitutional Document: It serves as the company's constitutional document, defining its scope, powers, and limitations.
Protection of Members: It protects the interests of the company's members by clearly defining the objectives and limiting their liability.
External Communication: It provides clarity to external parties, such as investors, creditors, and regulatory authorities, regarding the company's objectives and powers.
https://seribangash.com/difference-public-and-private-company-law/
Binding Authority: The company and its members are bound by the provisions of the MOA. Any action taken beyond its scope may be considered ultra vires (beyond the powers) of the company and therefore void.
Amendment of MOA:
While the MOA lays down the company's fundamental principles, it is not entirely immutable. It can be amended, but only under specific circumstances and in compliance with legal procedures. Amendments typically require shareholder
2. CDF Corporation
CDF Corporation is an international company that specializes in the manufacture
and sale of high quality liners and flexible packaging. Our diverse technical and
production capabilities make CDF the international leader in the production of liners
for pails, drums, bag-in-box and intermediate bulk containers.
3. CDF Corporation
CDF’s engineering and sales teams collaborate with each customer to design new
products or modify existing ones. Our involvement can range from liner selection
to full systems integration. We’ve been in business for over 40 years - with that
level of experience we can offer a variety of package designs for a wide array of
industries.
4. Global Capabilities
As an international company, CDF has ready access to the latest in design and
emerging technologies. While our primary manufacturing base is in the United
States, CDF also has production facilities in Europe for the EU.
5. CDF Products for Drums & Pails
CDF offers the industry's most comprehensive selection of liners, strainers, dust
caps, cover sheets and lids for drums and pails.
6. CDF Products for IBCs
CDF manufactures intermediate bulk container liners using the most advanced
technology in the industry.
7. Cheer Pack® Consumer Packaging
The Cheer Pack is a flexible pouch for packaging liquids, such as food,
beverages, cosmetics, industrial inks and gels, etc.
8. Cheertainer® Bag in Box
A smart alternative to traditional packaging, the Cheertainer is an innovative,
flexible package that flattens the competition. It is a gusseted, form-fit multi-ply
bag that gives you the best of both worlds; the flexibility of a bag-in-box, as well as
the benefits of a rigid container.
10. Cheertainer Benefits
Excellent quality due to superior seam strength
Fills without air = no foaming or splashing
Improved cleanliness
Efficient palletizing
Barrier films available
99.9% dispense without surging or glugging
UN certifiable
Accurate flow with no glugging
11. Cheertainer Sustainability Benefits
Ships flat for economical storage and shipping (10 to 1 ratio)
Less plastic than pails, bottles and rigid cubes
Requires less storage space
Reduces transportation and storage costs
Reduces use of fuel and greenhouse gas emissions
13. 20L Bag-in-Box vs. 20L Open Head Pail
Weight: 3.8 oz. Weight: 2.75 lbs.
Qty/TL empty: 64,800 bags Qty/TL empty: 6,500 pails
14. Cheertainer vs. Pillow Style
Filling
Form-fit fills more easily than a pillow as the fitment is always in the proper
position
Flex Cracking
Form-fit reduces flex cracking due to lack of folds in the bag and the perfect fit in
the box
Evacuation
Form-fit allows for full dispensing because
product does not get trapped in the folds
Pillow style Form-fit style
15. World Class Quality Leader
Using state of the art equipment and quality control standards of the highest
caliber, CDF1 Smart Seal Technology™ ensures the ultimate reliability of
Cheertainer and IBC liners.
Proprietary CDF1 Smart Seal Technology optimizes precision and consistency
through monitoring the temperature, time and pressure of every seal on every
liner.
16. CDF Control Plan
Receiving Inspection
Documentation Review
Process Parameter Design
In-Process Audit
100% Inspection Detail
17. Receiving Inspection Details
Certificate of Approval (COA) received with each shipment
Film shipments are certified for:
Tensile and elongation – ASTM D-882
Coefficient of friction (COF) – ASTM D-1894
Film gauge
18. Documentation Review
A cross functional team reviews each job’s documentation package for accuracy
Documents include:
Customer specification
Product specification
Operating work instructions
19. Process Parameter Design
Critical processing parameters are determined by the use of DOE’s (Design of
Experiments) as required
Processing parameters stored within our recipe file and restored for each job
run
Use CDF1 Smart Seal Technology system to monitor our critical processing
characteristics
20. CDF1 Smart Seal Technology
Supervisory Control and Data Acquisition (SCADA)
SCADA software allows CDF to monitor, measure and store data on every seal
of every bag we make
Can recall any of the machine conditions that contributed to the building of the
liner
21. Process Parameters Monitoring -
Tolerance
Component Upper and
Lower Limit
Tolerance Limit Alarm
Indicator
Selectable Machine Control
Stop (due to the tolerance
limits)
22. Process Monitoring
Select Component
Real Time Monitoring of:
» Seal Temperature
» Seal Dwell
» Seal Pressure
»
23. Process Monitoring
SCADA: shows temperature
drop when system stopped
Real-time process
monitoring of every seal
Alarms set if system
deviates from acceptable
System restarted
range
24. In-Process Audit
Perform first piece, last piece and hourly audits
Include the following:
Hydrostatic fitment test
Leak test
Dimensional compliance
100% visual product inspection
25. Defect Data
Defect data is posted real time on our “shared drive”
Employees are trained to react to any unusual process events
Data drives our continuous improvement activities
26. Product Traceability
All liners are printed with a time and date stamp, job number, part number and
sequence
27. Continuous Improvement Techniques
CDF Utilizes
Mistake proofing strategies
Team brainstorming
Cause and Effect Diagrams
Cause and Effect Matrix’s
5 Why’s
Verification of implemented strategies
Process capability studies
Design of Experiments
28. Certifications
ISO 9001:2008-registered company
All liners are made from FDA approved materials for food contact
Kosher certified
Manufacturing facilities comply with Good Manufacturing Practice (GMP)
standards
Multiple certified Six Sigma Black Belts on our manufacturing team
29. Cheertainer, The Total Package
Technical expertise
State of the art technology
Box design & solutions
Fitment solutions
Filling equipment partners
Film expertise & resources
Global capabilities
30. Cheertainer Contact Us
To learn more about becoming sustainable with Cheertainer bag-in-box,
visit CDF's website www.cdf1.com.
To speak with a sales representative,
call 800.443.1920 or 508.591.6732