Presentation from 2015 Association of Dressings and Sauces Technical Meeting by Dr. Claire Sand titled: GFSI, BRC, SQF and beyond where food safety is heading and packaging’s role in getting us there.
With 30 years of experience across the food science and packaging spectrum, Dr Claire Sand through her company, Packaging Technology & Research, offers clients solutions using Strategy, Technology, Consulting and coaching.
Want to know more about items reviewed in this presentation? Reach out to Dr Sand on Linked In - https://www.linkedin.com/in/clairekoelschsand
Want to keep learning? View more presentations at http://www.packagingtechnologyandresearch.com/thought-leadership.html
Dr. Claire Sand | Owner, Packaging Technology & Research, LLC; Adjunct Professor, Michigan State University; Columnist for Food Technology Magazine
http://www.packagingtechnologyandresearch.com/
FDA's Case for Quality: What, Why, and How? Changing the Regulatory ParadigmGreenlight Guru
Top-quality medical devices help the FDA better protect and promote public health. And one of the top priorities for FDA's medical devices center is a focus on quality.
The FDA launched the Case for Quality in 2011 following an in-depth review of device quality data and feedback from both FDA and industry stakeholders.
This program allows the FDA to recognize device manufacturers that are capable of consistently producing high-quality devices and continuously improving.
Greenlight Guru is partnering with FDA CDRH to help spread the word and promote the Case for Quality initiative and its benefits to the medical device industry. This is the first of four presentations, learn about the others at greenlight.guru.
Key points in this presentation:
-Learn about CfQ – What it is, why we are doing it, and how we are engaging
-Introduce pilot programs – Provide summary detail on various pilots at CDRH and associated with CfQ
-Regulatory paradigm – How is FDA rethinking the regulatory engagement
Watch this presentation, by Franciso Vicenty, the Case for Quality Manager of the FDA, here: https://www.greenlight.guru/webinar/fda-case-for-quality
Is your fleet prepared to meet the new food safety requirements under FSMA? Learn about the regulations and how to keep food safe in the supply chain from end to end.
Presentation from 2015 Association of Dressings and Sauces Technical Meeting by Dr. Claire Sand titled: GFSI, BRC, SQF and beyond where food safety is heading and packaging’s role in getting us there.
With 30 years of experience across the food science and packaging spectrum, Dr Claire Sand through her company, Packaging Technology & Research, offers clients solutions using Strategy, Technology, Consulting and coaching.
Want to know more about items reviewed in this presentation? Reach out to Dr Sand on Linked In - https://www.linkedin.com/in/clairekoelschsand
Want to keep learning? View more presentations at http://www.packagingtechnologyandresearch.com/thought-leadership.html
Dr. Claire Sand | Owner, Packaging Technology & Research, LLC; Adjunct Professor, Michigan State University; Columnist for Food Technology Magazine
http://www.packagingtechnologyandresearch.com/
FDA's Case for Quality: What, Why, and How? Changing the Regulatory ParadigmGreenlight Guru
Top-quality medical devices help the FDA better protect and promote public health. And one of the top priorities for FDA's medical devices center is a focus on quality.
The FDA launched the Case for Quality in 2011 following an in-depth review of device quality data and feedback from both FDA and industry stakeholders.
This program allows the FDA to recognize device manufacturers that are capable of consistently producing high-quality devices and continuously improving.
Greenlight Guru is partnering with FDA CDRH to help spread the word and promote the Case for Quality initiative and its benefits to the medical device industry. This is the first of four presentations, learn about the others at greenlight.guru.
Key points in this presentation:
-Learn about CfQ – What it is, why we are doing it, and how we are engaging
-Introduce pilot programs – Provide summary detail on various pilots at CDRH and associated with CfQ
-Regulatory paradigm – How is FDA rethinking the regulatory engagement
Watch this presentation, by Franciso Vicenty, the Case for Quality Manager of the FDA, here: https://www.greenlight.guru/webinar/fda-case-for-quality
Is your fleet prepared to meet the new food safety requirements under FSMA? Learn about the regulations and how to keep food safe in the supply chain from end to end.
How to Prepare for the New EU In Vitro Diagnostics RegulationsGreenlight Guru
Agreement was reached on the eagerly awaited new EU In Vitro Diagnostic Regulations (IVDR) earlier this year.
The IVDR will significantly change the way IVDs bear the CE mark, and it will include a completely new risk-based classification system.
Now 80% of all IVDs will need to be certified by a notified body under the IVDR where as before, only 20% needed to under the IVD Directive.
The new IVDR is expected to be formally published in late 2016 or early 2017, and there will be a five-year transition period to be compliant.
Many forward thinking IVD companies are already developing their plans for compliance now to gain strategic advantages over their competitors.
This presentation includes:
-Why the European regulations are changing
-What does the new regulation mean for IVD manufactures
-How to classify your IVD using the new risk-based classification system
-How to evaluate your existing clinical evidence to know if new studies will be needed to support your CE mark
-An overview of all the most significant changes brought by the IVDR
-What IVD manufactures can do to start preparing now
Watch the presentation here: https://www.greenlight.guru/webinar/eu-in-vitro-diagnostic-regulations-ivdr
In today’s complex global supply chain, proper supplier qualification is essential for avoiding supply chain failures and maintaining traceability of products.
There have been numerous public health crises in various industries regulated by the US Food and Drug Administration (FDA) related to contamination or adulteration of material along the supply chain.
Under Food Safety modernization Act (FSMA) Food and Drug Administration (FDA) issued final rule for Foreign Supplier Verification Programs (FSVP) on November 13, 2015
Consumers more than ever are looking for businesses to take more responsibility for problems that exist deep within the global supplier network, from worker exploitation, sustainable sourcing to single-use disposable products.
Join SAI Global and Verisio for a free 1-hour webinar, to learn how to embed an ethical approach to your business. To request the recording link please email information@saiglobal.com.
5 Predictions for the Medical Device Industry in 2018 (and how you can prepare)Greenlight Guru
What should the medical device industry expect in 2018?
Great question.
From ISO 13485 being revised in 2016, the EU MDR / IVDR being revised in 2017, and the MDSAP program going live in 2017, regulatory changes have been rampant and significant for medical device professionals.
This presentation covers:
- Why you should expect it to be harder for devices to get to market and stay there in the EU
- How to avoid the mad dash to update ISO 13485 certification before the deadline
- Where the latest revision of ISO 14971 is and when to expect the next update
- About Health Canada and their MDSAP deadline
- Why companies are shifting from being compliance-focused to quality-focused
Watch the presentation, commentated by Greenlight Guru's founder Jon Speer, here: https://www.greenlight.guru/webinar/2018-medical-device-industry-predictions
Building A Global Pharmaceutical Traceability FoundationSupplyScape
Traceability of pharmaceutical products as they move through the global supply chain. Regulations, technology standards, trading partner interoperability can all be barriers for companies seeking to gain the benefits of supply chain visibility and collaboration. Join SupplyScape in reviewing the key considerations and common misconceptions about pharmaceutical traceability.
Your Best Recall is the One You Never Have to DoSparta Systems
Regardless of industry, the best recalls are the ones that never happen. Recalls are not only costly to a company’s bottom line, but also to its reputation. Since so many entities are involved in the process of manufacturing, packaging, and distributing a finished product, it’s crucial to have insight into each link in the supply chain to avoid a costly recall.
Learn how the disclosure landscape is constantly changing, improving and then changing again – and the effects these new regulations and trends have on your business’s Disclosure Management Cycle.
How to Prepare for the New EU In Vitro Diagnostics RegulationsGreenlight Guru
Agreement was reached on the eagerly awaited new EU In Vitro Diagnostic Regulations (IVDR) earlier this year.
The IVDR will significantly change the way IVDs bear the CE mark, and it will include a completely new risk-based classification system.
Now 80% of all IVDs will need to be certified by a notified body under the IVDR where as before, only 20% needed to under the IVD Directive.
The new IVDR is expected to be formally published in late 2016 or early 2017, and there will be a five-year transition period to be compliant.
Many forward thinking IVD companies are already developing their plans for compliance now to gain strategic advantages over their competitors.
This presentation includes:
-Why the European regulations are changing
-What does the new regulation mean for IVD manufactures
-How to classify your IVD using the new risk-based classification system
-How to evaluate your existing clinical evidence to know if new studies will be needed to support your CE mark
-An overview of all the most significant changes brought by the IVDR
-What IVD manufactures can do to start preparing now
Watch the presentation here: https://www.greenlight.guru/webinar/eu-in-vitro-diagnostic-regulations-ivdr
In today’s complex global supply chain, proper supplier qualification is essential for avoiding supply chain failures and maintaining traceability of products.
There have been numerous public health crises in various industries regulated by the US Food and Drug Administration (FDA) related to contamination or adulteration of material along the supply chain.
Under Food Safety modernization Act (FSMA) Food and Drug Administration (FDA) issued final rule for Foreign Supplier Verification Programs (FSVP) on November 13, 2015
Consumers more than ever are looking for businesses to take more responsibility for problems that exist deep within the global supplier network, from worker exploitation, sustainable sourcing to single-use disposable products.
Join SAI Global and Verisio for a free 1-hour webinar, to learn how to embed an ethical approach to your business. To request the recording link please email information@saiglobal.com.
5 Predictions for the Medical Device Industry in 2018 (and how you can prepare)Greenlight Guru
What should the medical device industry expect in 2018?
Great question.
From ISO 13485 being revised in 2016, the EU MDR / IVDR being revised in 2017, and the MDSAP program going live in 2017, regulatory changes have been rampant and significant for medical device professionals.
This presentation covers:
- Why you should expect it to be harder for devices to get to market and stay there in the EU
- How to avoid the mad dash to update ISO 13485 certification before the deadline
- Where the latest revision of ISO 14971 is and when to expect the next update
- About Health Canada and their MDSAP deadline
- Why companies are shifting from being compliance-focused to quality-focused
Watch the presentation, commentated by Greenlight Guru's founder Jon Speer, here: https://www.greenlight.guru/webinar/2018-medical-device-industry-predictions
Building A Global Pharmaceutical Traceability FoundationSupplyScape
Traceability of pharmaceutical products as they move through the global supply chain. Regulations, technology standards, trading partner interoperability can all be barriers for companies seeking to gain the benefits of supply chain visibility and collaboration. Join SupplyScape in reviewing the key considerations and common misconceptions about pharmaceutical traceability.
Your Best Recall is the One You Never Have to DoSparta Systems
Regardless of industry, the best recalls are the ones that never happen. Recalls are not only costly to a company’s bottom line, but also to its reputation. Since so many entities are involved in the process of manufacturing, packaging, and distributing a finished product, it’s crucial to have insight into each link in the supply chain to avoid a costly recall.
Learn how the disclosure landscape is constantly changing, improving and then changing again – and the effects these new regulations and trends have on your business’s Disclosure Management Cycle.
Top Risks in Global Supply Chains: Primary-Source Intelligence and Recommenda...Sustainable Brands
The globalization of supply chains, occurring in many industries these days, has created unforeseen challenges in ensuring the workers and environments by which products are now manufactured are treated ethically and responsibly. For a long time supplier audits used to be just paper- or spreadsheet-based, without much accompanying data analysis, aggregation or trending. That is now beginning to change, leading to new levels of sophistication in extracting intelligence from supply chain data. For this session, we are joined by two organization leading this shift: Intertek, the largest and longest running CSR auditing body conducting over 60,000 such audits each year and author of the Intertek Workplace Conditions Assessment (WCA), the fastest growing CSR audit report with over 15,000 participating factories to date; and Sedex, the world's largest collaborative platform for sharing supply chain data, with over 36,000 participating organizations representing 30 industry sectors and more than 24 million workers in more than 160 countries. The two will combine their latest observations for an analysis of critical supply chain risks around the world that executives should keep top of mind.
Experience guide to or implementation and compliance 2015Edifecs Inc
Ready to kick-off a compliance project? Don’t miss this webinar; leverage our experience to accelerate your compliance programs. Understand the certification options. Gain insight to assist your organization maintain compliance after project completion. Understand how certification and partner communication can protect your organization.
Blockchain is constantly revolutionizing various industries, and supply chain is one of the major ones. Many companies are already using blockchain in supply chain to reap the benefits of blockchain technology. But why is it necessary to use blockchain for supply chain management?
At the moment, the supply chain industries deal with a lot of issues. Among them, rapid changes in the market, issues with compliance and quality, lack of transparency, increasing corruption, high costs, etc., are prominent problems. This is where blockchain steps in.
Using blockchain in supply chain management comes with its fair share of benefits - peer-to-peer transaction settlement, audit transparency, tracking products, and consumer feedbacks, accurate costing info, better shipping data, etc. In fact, there are already many blockchain supply chain projects live at the moment working perfectly.
We at 101 Blockchains are driven to help you educate on blockchain technology with high-quality courses and certifications. Therefore, we offer specific courses geared to supply chain management as well. At present, we have two prominent courses that can help you understand the concepts better - Enterprise Blockchains and Supply Chain Management Course and Enterprise Blockchains and Trade Finance Course.
Learn more about these courses from here ->
https://academy.101blockchains.com/courses/blockchain-and-scm
https://academy.101blockchains.com/courses/enterprise-blockchains-and-trade-finance
Other than these, we have certification courses to help you become a skilled professional in no time. Learn more about these courses from here ->
Certified Enterprise Blockchain Professional (CEBP) course https://academy.101blockchains.com/courses/blockchain-expert-certification
Certified Enterprise Blockchain Architect (CEBA) course
https://academy.101blockchains.com/courses/certified-enterprise-blockchain-architect
Certified Blockchain Security Architect (CBSE) course
https://academy.101blockchains.com/courses/certified-blockchain-security-expert
Responsible Procurement: general status, trends and implementation. | Albert ...Albert Vilariño
Post published on Medium on 01/01/2017.
https://medium.com/@albert.vilarino/responsible-procurement-general-status-trends-and-implementation-7a3efbee2cfe#.9k4yx4yxn
In the Adani-Hindenburg case, what is SEBI investigating.pptxAdani case
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Kseniya Leshchenko: Shared development support service model as the way to ma...Lviv Startup Club
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Kyiv PMDay 2024 Summer
Website – www.pmday.org
Youtube – https://www.youtube.com/startuplviv
FB – https://www.facebook.com/pmdayconference
The world of search engine optimization (SEO) is buzzing with discussions after Google confirmed that around 2,500 leaked internal documents related to its Search feature are indeed authentic. The revelation has sparked significant concerns within the SEO community. The leaked documents were initially reported by SEO experts Rand Fishkin and Mike King, igniting widespread analysis and discourse. For More Info:- https://news.arihantwebtech.com/search-disrupted-googles-leaked-documents-rock-the-seo-world/
VAT Registration Outlined In UAE: Benefits and Requirementsuae taxgpt
Vat Registration is a legal obligation for businesses meeting the threshold requirement, helping companies avoid fines and ramifications. Contact now!
https://viralsocialtrends.com/vat-registration-outlined-in-uae/
Premium MEAN Stack Development Solutions for Modern BusinessesSynapseIndia
Stay ahead of the curve with our premium MEAN Stack Development Solutions. Our expert developers utilize MongoDB, Express.js, AngularJS, and Node.js to create modern and responsive web applications. Trust us for cutting-edge solutions that drive your business growth and success.
Know more: https://www.synapseindia.com/technology/mean-stack-development-company.html
Company Valuation webinar series - Tuesday, 4 June 2024FelixPerez547899
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Recruiting in the Digital Age: A Social Media MasterclassLuanWise
In this masterclass, presented at the Global HR Summit on 5th June 2024, Luan Wise explored the essential features of social media platforms that support talent acquisition, including LinkedIn, Facebook, Instagram, X (formerly Twitter) and TikTok.
Putting the SPARK into Virtual Training.pptxCynthia Clay
This 60-minute webinar, sponsored by Adobe, was delivered for the Training Mag Network. It explored the five elements of SPARK: Storytelling, Purpose, Action, Relationships, and Kudos. Knowing how to tell a well-structured story is key to building long-term memory. Stating a clear purpose that doesn't take away from the discovery learning process is critical. Ensuring that people move from theory to practical application is imperative. Creating strong social learning is the key to commitment and engagement. Validating and affirming participants' comments is the way to create a positive learning environment.
Event Report - SAP Sapphire 2024 Orlando - lots of innovation and old challengesHolger Mueller
Holger Mueller of Constellation Research shares his key takeaways from SAP's Sapphire confernece, held in Orlando, June 3rd till 5th 2024, in the Orange Convention Center.
3.0 Project 2_ Developing My Brand Identity Kit.pptxtanyjahb
A personal brand exploration presentation summarizes an individual's unique qualities and goals, covering strengths, values, passions, and target audience. It helps individuals understand what makes them stand out, their desired image, and how they aim to achieve it.
3.0 Project 2_ Developing My Brand Identity Kit.pptx
The Emerging Use of Community of Interest Networks to Manage Compliance within the Supply Chain
1. The emerging use of COIN (Community of Interest) networks to manage compliance reporting within the supply chain Presented at the 17th Australian HACCP Conference and 5th SQF International Conference August 2010 Melbourne, Australia Nigel Dalton-Brown, iCiX Asia
2. The SQF Code requires Compliance Communication 4.3 Specification and Product Development 4.3.2 Raw Materials 4.3.3 Packaging 4.3.4 Contract Service Providers 4.3.5 Contract Manufacturers 4.3.6 Finished Product Distribution 4.4 Attaining Food Safety 4.4.5 Incoming Goods and Services 4.4.6 Corrective and Preventative Action 4.6 Product Identification, Trace, Withdrawal and Recall 4.6.2 Product Trace 4.6.3 Product Withdrawal and Recall 5.3 Water and Ice Supply 5.3.1 Water Supply 5.3.3 Ice Supply 6.8 Monitoring Water Microbiology and Quality 6.8.3 Analysis 6.10 Supplier Approval 6.10.1 Selecting Approved Suppliers 6.10.2 Approved Supplier Program 6.10.3 Monitoring Approved Suppliers 6.10.4 Register 6.10.5 Records Supply 6.13 Allergen Control 6.13.2 Risk Assessment
3. How does it work in practice? Corrective actions also need to be sent out and actioned Also need to collect Certificates of Analysis from Laboratories and testing houses Buyer sends copies of policies and procedures to all suppliers We also need to carry out mock recalls and Product Withdrawals Distribute Policies and Procedures Collect Compliance Certificates Certificates of Analysis and Audits Corrective Actions Product Withdrawals and Recalls Now need to store and manage multiple certificates from multiple suppliers all with different expiry dates Now have multiple copies of policies and procedures across all suppliers Buyer sets up relationships with suppliers
8. Some open responses from our global survey A number of respondents expressed concern that Supplier Compliance Management was not getting the attention it deserved..... Supplier Compliance is an issue that is at times neglected when minor issue are ignored. However it is the minor issue that eventually contribute to major fallout's Totally ignored till it is too late. As part of the contract commencement, we request the required docs/certs before the contract is signed. Where we are not so good, is managing the document expiry during the life of the contract. My company does not have a central repository for tracking contracts let alone compliance. Each department is allowed to manage or not manage as they deem appropriate A real time system would be very helpful but cost is a constant constraint iCiX/IPcubed Global Survey into the perceived importance of compliance management – May 2010
11. And it’s expensive In 2003 Food Standards ANZ reported example recall costs Major retailer conducting national recall of 17,680 cartons of frozen processed chicken: press advertisements $51,521 stock costs $75,709 cost of recovery $119,425 labour costs $4,000 other associated costs $7,217 Total cost of recall $257,872 FSANZ did not account for consequential loss such as Loss of revenue Damage to brand Data from Food Standards ANZ, 2003
12. The current way of tracking compliance Distribution 64.2% lack coherent standards of what documents actually required 79.6% use a manual, labour intensive, paper based system (excel or a database) 44% deal with over 1,000 documents 50% do not remove suppliers for non-compliance because they could not track it well enough. Staff waste hours chasing missing documents out of date documents Generally inaccurate costly lower quality due to lack of tracking of COPQ exposes the organisation to risk Supply
13. A day in the life of.... “It’s a mind numbing, soul destroying, never ending task”
24. The COIN Approach Buyers post all their policies and procedures to their secure site. May also post technical specifications for suppliers to reference. Only ONE copy is posted on the COIN network. This single copy is then made available to relevant suppliers Each organisation, buyers and suppliers, joins and creates their own secure site The COIN network exists to provide many-to-many connections between trading partners Documents are no longer stored and collected. The key metadata is used to generate reminders and reports in real time. In the same way, suppliers post ONE copy of each relevant compliance certificate, PLUS key metadata, e.g. Type, expiry date, alergens/nutritional data, product specifications...
25. The COIN – COA’s and Audits Auditing and certification companies and laboratories are also part of the COIN. Buyers can request audits with the results posted onto the suppliers sites for viewing by the buyer.
26. The COIN - Recall Customers also join iCiX. This allows for recalls, CAR’s, smartforms, etc Buyers COIN A many to many Community of Interest Third Party Auditors Certification bodies Laboratories Customers Suppliers and subcontractors
27. Key Characteristics Each organisation has it’s own site The responsibility changes from “Buyer collects” to “Supplier publishes and shares” Communication paths created with third parties: Auditors, Laboratories, Customers and Regulators Documents are loaded only once Costs are shared across the industry
28. Follow on benefits of COIN networks Real time reports with high confidence Broadcast messages to suppliers Product Recall/Withdrawl in hours not days or months Corrective action requests with COPQ claims PDF online forms for compliance related work
30. The top three reasons for inaction Insufficient time Inadequate budget Insufficient administrative resources To counter the “no time”, 86% of respondents have decided that someone else (i.e. suppliers themselves or an independent third party) should take on the actual day to day grind of driving supplier participation in the purchasers ethics and compliance initiatives With COIN, suppliers carry out the day to day grind of publish documents. COIN also reduces unnecessary copies by approx 99% To circumvent the “no budget”, 75% of respondents have decided that suppliers should share or bear the cost of participating in the purchasers ethics and compliance initiatives Under COIN systems, everyone pays and so the costs are spread. The emerging solution has a great deal to do with collaboration COIN networks are by definition collaborative Source: Building an ethical supply chain. Michael Levin, 2008 Integrity Interactive Survey, 2008
43. Product recalls/withdrawals using iCiX We have an average completion rate of 77.1% within 2 hrs Client A is achieving 82.1% within 2hrs across 133 recipients
48. Janet, I need a Risk Management Assessment on our suppliers The assessment showed that there was a high risk of no management Risk Management Assessment..... Framework Software (UK)
50. FREE iCiX-RECALL Sign up to receive free use of iCiX-RECALL module for 3 years Thank You Nigel Dalton-Brown, iCiX Asia
Editor's Notes
Effective hourly cost based on annual salary of $60k with 1.5 uplift to account for sick days, leave, PC heating.... etc.
Anecdotal evidence of talking a large number of clients and prospects gives me the following four types of
Research has shown that organisations and individuals fail to comply for various resaons cost of regulatory compliance insufficient resources and expertise to address compliance requirements lack of knowledge of requirements or even indifferenceFrom a 2008 survey by Integrity InteractiveTo counter the “no time”, 86% of respondents have decided that someone else (i.e. Suppliers themselves or and independent third party) should take on the actual day to day grind of driving supplier participation in the purchasers ethics and compliance initiativesTo circumvent the “no budget”, 75% of respondents have decided that suppliers should share or bear the cost of participating in the purchasers ethics and compliance initiatives
From a 2008 survey by Integrity InteractiveTo counter the “no time”, 86% of respondents have decided that someone else (i.e. Suppliers themselves or and independent third party) should take on the actual day to day grind of driving supplier participation in the purchasers ethics and compliance initiativesTo circumvent the “no budget”, 75% of respondents have decided that suppliers should share or bear the cost of participating in the purchasers ethics and compliance initiatives
Effective hourly cost based on annual salary of $60k with 1.5 uplift to account for sick days, leave, PC heating.... etc.
Research has shown that organisations and individuals fail to comply for various resaons cost of regulatory compliance insufficient resources and expertise to address compliance requirements lack of knowledge of requirements or even indifferenceOur recetn survey, 64.2% of respondants said they were Partially or not fully aware of their regulatory responsibilities for managing supplier compliance