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Ongoing, monthly FSMA webcast series featuring The Acheson Group. In the April 2018 session, Cameron Prince, Senior Food Safety Director with The Acheson Group, joined us for an update on current FSMA activities and to discuss the Safe Food For Canadians Act. Cameron provided an overview of the key elements of the act and proposed regulations and the impact on current food safety environment. To learn more about this ongoing series, visit www.FSMAFridays.com.
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SQF has added an unannounced audit requirement making it more important than ever for food industry operations to be aware of common mistakes that could influence not only SQF audit results, but also food quality and safety. SQF’s LeAnn Chuboff and Alchemy Systems' Holly Mockus outline: How to identify SQF non-conformances from desk audits. How to address the top 10 SQF non-conformances. How to mitigate food safety risks from non-conformances.
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Ongoing, monthly FSMA webcast series featuring The Acheson Group. In the April 2018 session, Cameron Prince, Senior Food Safety Director with The Acheson Group, joined us for an update on current FSMA activities and to discuss the Safe Food For Canadians Act. Cameron provided an overview of the key elements of the act and proposed regulations and the impact on current food safety environment. To learn more about this ongoing series, visit www.FSMAFridays.com.
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SQF has added an unannounced audit requirement making it more important than ever for food industry operations to be aware of common mistakes that could influence not only SQF audit results, but also food quality and safety. SQF’s LeAnn Chuboff and Alchemy Systems' Holly Mockus outline: How to identify SQF non-conformances from desk audits. How to address the top 10 SQF non-conformances. How to mitigate food safety risks from non-conformances.
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Validation of preventive controls is where the rubber meets the road in terms of prevention. You can develop a food safety plan, implement the plan and verify the plan, but if your data does not prove that you are actually preventing food safety problems
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The Process Validation Guidelines (January 2011) and the EU Annex 15: Qualification and Validation (October 2015) outline the general principles and approaches the two regulatory bodies consider appropriate elements of process validation for the manufacture of human and animal drugs and biological products, including Active Pharmaceutical Ingredients (APIs).
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Semelhante a Business Cont Pres041209
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.
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An effective complaint handling system is an extremely important part of any quality system. Manufacturers should understand that any complaint received on a product shall be evaluated and, if necessary, thoroughly investigated and analyzed, and corrective action shall be taken. The results of this evaluation should lead to a conclusion regarding whether the complaint was valid, what the root cause of the complaint was, and what action is necessary to prevent further occurrences.
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An effective complaint handling system is an extremely important part of any quality system. Manufacturers should understand that any complaint received on a product shall be evaluated and, if necessary, thoroughly investigated and analyzed, and corrective action shall be taken.
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Many regulated companies preparing for FDA inspections are not prepared and the outcome can be negative as we see all the time with enforcement actions. This seminar provides the fundamentals and the ground rules on how to prepare for and survive an FDA inspection no matter if you are a Class I, II, III device or a pharmaceutical or biologics manufacturer.
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Many regulated companies preparing for FDA inspections are not prepared and the outcome can be negative as we see all the time with enforcement actions. This seminar provides the fundamentals and the ground rules on how to prepare for and survive an FDA inspection no matter if you are a Class I, II, III device or a pharmaceutical or biologics manufacturer.
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Many regulated companies preparing for FDA inspections are not prepared and the outcome can be negative as we see all the time with enforcement actions. This seminar provides the fundamentals and the ground rules on how to prepare for and survive an FDA inspection no matter if you are a Class I, II, III device or a pharmaceutical or biologics manufacturer.
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FDA recently endorsed the Risk Management approach described in ICH Q9. I presented this a year ago to ASQ Philadelphia. Still relevant today!
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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.
Building A Global Pharmaceutical Traceability Foundation
Building A Global Pharmaceutical Traceability Foundation
SupplyScape
Regulatory and Compliance Seminars | Courses | Conferences - Globalcompliancepanel
Documenting software for fda submissions
Documenting software for fda submissions
GlobalCompliancePanel
Laboratory Medicine Best Practices (LMBP)
Laboratory Medicine Best Practices (LMBP)
Sherese Bleechington Garrett
In the food industry, along with the demanding quality requirements, manufacturers need to serve growing customer expectations, food quality management software offers numerous benefits in this case. Check this presentation to dive in the details
Quality Management System For Food Manufacturing Industry
Quality Management System For Food Manufacturing Industry
BM QualityMaster
When medical device companies consider Agile development methods, they often run into the key criticism that Agile groups produce little to no documentation, and that Agile stands in contradiction to the lifecycle standards outlined in IEC 62304.
documenting software for fda submissions
documenting software for fda submissions
GlobalCompliancePanel
food safe level 1 that shows up totally fine can contain microorganisms — illness causing microbes, infections, or parasites — that can make you wiped out. You ought to never taste a food safe course to decide whether it is protected to eat.
Food safety rules and regulations.pdf
Food safety rules and regulations.pdf
SuperStudyLearningCe
inspecao graos
Grain handling eng_hb_web
Grain handling eng_hb_web
wagner campagnaro
Semelhante a Business Cont Pres041209
(20)
Your Best Recall is the One You Never Have to Do
Your Best Recall is the One You Never Have to Do
Deploying A Crisis Management and Business Continuity Approach to Product Tam...
Deploying A Crisis Management and Business Continuity Approach to Product Tam...
Complaint handling-management-denmark
Complaint handling-management-denmark
Complaint handling-management-denmark
Complaint handling-management-denmark
Fda at-my-facility-cape-town
Fda at-my-facility-cape-town
why FDA at my Facility is, and what do I do During an Inspection
why FDA at my Facility is, and what do I do During an Inspection
IFC+Guidelines+for+Coaching+on+Food+Safety_ENG.pdf
IFC+Guidelines+for+Coaching+on+Food+Safety_ENG.pdf
Complaint handling-management-cape-town
Complaint handling-management-cape-town
Fda at-my-facility-singapore
Fda at-my-facility-singapore
An Introduction To Risk Management Professional Societies
An Introduction To Risk Management Professional Societies
Meditech Written Case Analysis
Meditech Written Case Analysis
Session for Introduction to Quality Improvement By Lisa
Session for Introduction to Quality Improvement By Lisa
Requirements for Establishing an Effective Cleaning Validation Program
Requirements for Establishing an Effective Cleaning Validation Program
Building A Global Pharmaceutical Traceability Foundation
Building A Global Pharmaceutical Traceability Foundation
Documenting software for fda submissions
Documenting software for fda submissions
Laboratory Medicine Best Practices (LMBP)
Laboratory Medicine Best Practices (LMBP)
Quality Management System For Food Manufacturing Industry
Quality Management System For Food Manufacturing Industry
documenting software for fda submissions
documenting software for fda submissions
Food safety rules and regulations.pdf
Food safety rules and regulations.pdf
Grain handling eng_hb_web
Grain handling eng_hb_web
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Transformation is even harder than we thought “Only 22% of companies successfully carry out transformation. The failure rate was 78%.” “Often the business value of digital transformation is not realized. One of the most common causes is an abundance of technology projects, not a true business culture transformation” - Phil Le-Brun, Enterprise Strategist, AWS
Organizational Transformation Lead with Culture
Organizational Transformation Lead with Culture
Seta Wicaksana
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How to Get Started in Social Media for Art League City
Eric T. Tung
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Uneak White's Personal Brand Exploration Presentation
Uneak White's Personal Brand Exploration Presentation
uneakwhite
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Phases of Negotiation .pptx
Phases of Negotiation .pptx
nandhinijagan9867
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Insurers' journeys to build a mastery in the IoT usage
Insurers' journeys to build a mastery in the IoT usage
Matteo Carbone
Value proposition canvas Jobs to be done Customer pains Customer gains Gain creators Pain relievers
Value Proposition canvas- Customer needs and pains
Value Proposition canvas- Customer needs and pains
P&CO
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Cracking the Cultural Competence Code.pptx
Cracking the Cultural Competence Code.pptx
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Business Model Canvas (BMC)- A new venture concept
P&CO
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How to Get Started in Social Media for Art League City
Uneak White's Personal Brand Exploration Presentation
Uneak White's Personal Brand Exploration Presentation
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Insurers' journeys to build a mastery in the IoT usage
Insurers' journeys to build a mastery in the IoT usage
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Business Cont Pres041209
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