10 Steps To Import Seafood Into the United States From China 进口水产品到美国的十大步骤： FDA进口检验流程
•
2 likes•1,469 views
Presentation given at the 2011 Chinese Seafood and Fisheries Expo 2011, Qingdao China. "This seminar will provide an introduction to U.S. FDA Requirements and Procedures and the 2011 Food Safety Modernization Act for seafood exporters. Mr. Quinn is an attorney with expertise in FDA HACCP, food label reviews, FDA inspections and FDA import alerts." "此次研讨会将向水产品出口商详细介绍美国FDA的法律法规要求和 进口步骤，以及2011年食品安全现代化法案的相关政策。昆天佑 律师精通FDA 的HACCP体系合规性、食品标签审核、FDA检测及 FDA进口警示等领域"。 © 2011 http://www.fdaimports.com and http://www.exporttousa.com.cn
Report
Share
Report
Share
![Rick D. Quinn, Esq. ,[object Object],[object Object],[object Object],FINRA 分析师 资产管理 资深律师 FDAImports.com and ExportToUsa.com.cn](data:image/gif;base64,R0lGODlhAQABAIAAAAAAAP///yH5BAEAAAAALAAAAAABAAEAAAIBRAA7)
Recommended
1.a introducción a la fda
The FDA's Latin America Office (LAO) aims to advance the FDA's mission of protecting public health internationally by coordinating activities in Latin America, building relationships with foreign regulators, and leveraging information to better monitor imported products and ensure safety; key challenges include rising imports and more complex global supply chains, and future opportunities include increasing inspections, product mapping, and collaboration with industry and foreign governments.
The U.S. FDA Food Safety Modernization Act (For Exporters To The Us)
The Food Safety Modernization Act (FSMA) was signed into law in 2011, amending the Food, Drug and Cosmetic Act. It shifts responsibility for food safety to food processors and importers and requires facilities to register with the FDA. FSMA implements new regulations around foreign supplier verification, preventive controls for food facilities, produce safety, and third party auditors. It also imposes new fees for facility reinspections, product reconditioning, and import refusals. FSMA will be implemented in phases through 2016 with increased foreign food facility inspections.
U.S. FDA Food Safety Modernization Act (FSMA) Seminar (English)
The U.S. Food and Drug Administration (FDA) Food Safety Modernization Act (FSMA) presents many important changes for companies exporting food to the United States.
US FDA Food Safety Modernization Act-Future Impact on Asia
This document provides an overview of the U.S. Food and Drug Administration's Food Safety Modernization Act and its future impact on food importers and manufacturers in Asia. It discusses key components of the act related to prevention, inspections and compliance, import safety, and enhanced partnerships. The act aims to shift the U.S. food safety focus from response to prevention. It establishes standards for food production and imports and increases inspections of domestic and foreign facilities. Foreign manufacturers will face greater oversight and responsibility to meet new food safety requirements.
1.b alcances de la nueva ley de inocuidad de alimentos del fda
The document summarizes the Food Safety Modernization Act and the FDA's proposed produce safety regulations. It discusses why the law was needed due to issues like globalization and the increasing complexity of the food supply. It then outlines key provisions of the law around prevention, inspections/compliance, imports, and partnerships. It focuses on new requirements for importers to verify the safety of foreign suppliers and facilities. Finally, it discusses the FDA's approach to implementing the new rules through education, outreach, and flexibility.
U.S. FDA Food Safety Modernization Act (FSMA) for Customs Brokers
Learn about the new regulations under the U.S. FDA Food Safety Modernization Act (FSMA), including new requirements for U.S. Agents.
Dietary Supplements, Combination Products, and Veterinary Medicine
This document summarizes a presentation about solving FDA legal challenges for life sciences companies. It discusses dietary supplements, combination products, and veterinary medicine. For dietary supplements, it covers basics like definitions; new dietary ingredients and notification requirements; labeling rules for claims, ingredients, and nutrition; good manufacturing practices; and adverse event reporting. For combination products, it discusses primary mode of action determination, the request for designation process, applicable regulations, and application requirements. Veterinary medicine topics are also briefly mentioned.
David Acheson's Webinar Slides on Food Safety Legislation
The Food Safety Modernization Act is the most sweeping reform of U.S. food safety laws since 1938. It seeks to shift the focus from responding to contamination to preventing it. Key provisions include mandatory inspection frequencies for food facilities based on risk, expanded access to food facility records, and new mandatory recall authority for FDA. The act increases regulation and oversight of both domestic and imported food. Full implementation will require additional resources and take time. Facilities, importers, laboratories and other stakeholders must understand and prepare for coming changes to food safety laws and oversight.
Recommended
1.a introducción a la fda
The FDA's Latin America Office (LAO) aims to advance the FDA's mission of protecting public health internationally by coordinating activities in Latin America, building relationships with foreign regulators, and leveraging information to better monitor imported products and ensure safety; key challenges include rising imports and more complex global supply chains, and future opportunities include increasing inspections, product mapping, and collaboration with industry and foreign governments.
The U.S. FDA Food Safety Modernization Act (For Exporters To The Us)
The Food Safety Modernization Act (FSMA) was signed into law in 2011, amending the Food, Drug and Cosmetic Act. It shifts responsibility for food safety to food processors and importers and requires facilities to register with the FDA. FSMA implements new regulations around foreign supplier verification, preventive controls for food facilities, produce safety, and third party auditors. It also imposes new fees for facility reinspections, product reconditioning, and import refusals. FSMA will be implemented in phases through 2016 with increased foreign food facility inspections.
U.S. FDA Food Safety Modernization Act (FSMA) Seminar (English)
The U.S. Food and Drug Administration (FDA) Food Safety Modernization Act (FSMA) presents many important changes for companies exporting food to the United States.
US FDA Food Safety Modernization Act-Future Impact on Asia
This document provides an overview of the U.S. Food and Drug Administration's Food Safety Modernization Act and its future impact on food importers and manufacturers in Asia. It discusses key components of the act related to prevention, inspections and compliance, import safety, and enhanced partnerships. The act aims to shift the U.S. food safety focus from response to prevention. It establishes standards for food production and imports and increases inspections of domestic and foreign facilities. Foreign manufacturers will face greater oversight and responsibility to meet new food safety requirements.
1.b alcances de la nueva ley de inocuidad de alimentos del fda
The document summarizes the Food Safety Modernization Act and the FDA's proposed produce safety regulations. It discusses why the law was needed due to issues like globalization and the increasing complexity of the food supply. It then outlines key provisions of the law around prevention, inspections/compliance, imports, and partnerships. It focuses on new requirements for importers to verify the safety of foreign suppliers and facilities. Finally, it discusses the FDA's approach to implementing the new rules through education, outreach, and flexibility.
U.S. FDA Food Safety Modernization Act (FSMA) for Customs Brokers
Learn about the new regulations under the U.S. FDA Food Safety Modernization Act (FSMA), including new requirements for U.S. Agents.
Dietary Supplements, Combination Products, and Veterinary Medicine
This document summarizes a presentation about solving FDA legal challenges for life sciences companies. It discusses dietary supplements, combination products, and veterinary medicine. For dietary supplements, it covers basics like definitions; new dietary ingredients and notification requirements; labeling rules for claims, ingredients, and nutrition; good manufacturing practices; and adverse event reporting. For combination products, it discusses primary mode of action determination, the request for designation process, applicable regulations, and application requirements. Veterinary medicine topics are also briefly mentioned.
David Acheson's Webinar Slides on Food Safety Legislation
The Food Safety Modernization Act is the most sweeping reform of U.S. food safety laws since 1938. It seeks to shift the focus from responding to contamination to preventing it. Key provisions include mandatory inspection frequencies for food facilities based on risk, expanded access to food facility records, and new mandatory recall authority for FDA. The act increases regulation and oversight of both domestic and imported food. Full implementation will require additional resources and take time. Facilities, importers, laboratories and other stakeholders must understand and prepare for coming changes to food safety laws and oversight.
Fda
This document outlines the FDA's proposed plans and programs for regulating halal products in the Philippines. It discusses establishing a Halal Unit within the FDA to oversee licensing of halal establishments, registration of halal products, and post-market surveillance. Products that would be regulated include food, cosmetics, pharmaceuticals, and medical devices. The FDA plans to coordinate with other agencies like the NCMF and ensure its halal policies are consistent with national standards. Challenges include developing clear interagency policies and regulations on halal as well as expanding laboratory testing capabilities for halal products.
US FDA Regs & Modernization Act 2012
The document provides an overview of U.S. FDA regulations for exporting food and beverages to the U.S., including the Food Safety Modernization Act. It discusses the FDA's jurisdiction and structure, key food regulations on labeling, ingredients and claims. It also summarizes provisions of the FSMA relating to prevention of food hazards, mandatory inspections, import safety through programs like the Foreign Supplier Verification Program. The seminar aims to help exporters understand and comply with complex U.S. food safety rules.
Kerr, Jason Final Poster
Gilead Sciences prepares a Certificate of Pharmaceutical Product (CPP) application to submit to the FDA to export their drug Harvoni to Mongolia. A CPP provides essential information about a drug product for countries without strong regulatory systems. Gilead submits documentation about Harvoni's registration, formulation, labeling, and manufacturing to the FDA. If approved, the FDA issues an authenticated CPP valid for 24 months. Mongolia then reviews Gilead's drug application including the CPP to determine if Harvoni can be sold in their country. CPPs help ensure imported drugs meet good manufacturing practice standards and quality when countries lack regulatory capacity to verify this themselves.
FDA Export Certificates
Manufacturers that export FDA-regulated products such as drugs and medical devices from the US are oftentimes required to provide a certificate prepared by the FDA which confirms the product’s regulatory and marketing status...
AmCham Seminar
The document discusses new legislation and regulations around food safety in the United States. It outlines the Food Safety Modernization Act, which aims to modernize the food safety system by shifting from reactive to preventative response. Key points of the new law include increased mandatory inspections of domestic and foreign facilities by the FDA, requiring food safety plans and prevention controls, and more import certification requirements for foreign exporters. The changes are expected to significantly impact Chinese exporters through new registration, record access, inspection and food safety standard requirements.
DSHEA
1) The Dietary Supplement Health and Education Act of 1994 (DSHEA) defines and regulates dietary supplements in the US, placing them in the food category and requiring manufacturers to ensure safety and accurate labeling.
2) Use of dietary supplements increased after DSHEA, with over half of US adults regularly using supplements by 2003-2006, especially women.
3) DSHEA aimed to ensure continued consumer access to supplements while providing more information, without changing their status as foods regulated by FDA for safety.
Are you ready to implement FDA Food Safety Modernization Act?
The document discusses the Food Safety Modernization Act (FSMA), which establishes new rules for food safety in the United States. It was signed into law in 2011 to better protect public health by strengthening the food safety system from farm to table. The FSMA impacts farmers, food manufacturers, transporters, importers and others. Its major components establish requirements for preventive controls, inspections and compliance, imported food safety, and enhanced partnerships between food safety agencies. Compliance dates vary depending on business size, with larger businesses required to comply sooner.
Acheson / Bode Food Safety Law 01-06-11
The Food Safety Modernization Act grants the FDA new authorities to regulate food safety, including mandatory recall authority, expanded access to facility records, and increased oversight of imported foods. Key changes include increased inspection frequencies for domestic and foreign facilities based on risk factors. The FDA will also be able to require certification of imported foods by third-party auditors. Facilities that produce, process or distribute food will need to implement food safety plans and be prepared for greater regulatory scrutiny of their operations and records. The new law aims to shift the FDA's focus from response to prevention of foodborne illness outbreaks.
Avoiding Pitfalls in the Regulatory Path - MaRS Best Practices
Innovating in the life sciences and health-care sector? You can’t escape the regulators! Before you make a costly mistake, learn from the experts who have been through the process before.
Whether you’re working on a therapeutic, an in vitro diagnostic or a medical device, come find out how to identify and mitigate challenges along the path to regulatory approval.
FDA Globalization Act (Dingell Bill) Summary Jan 2009
The Food and Drug Administration Globalization Act of 2009 strengthens oversight of food, drug, medical device, and cosmetic safety. It requires facilities in the US and abroad to register annually with the FDA and pay fees to fund increased inspections. Safety plans and compliance with good manufacturing practices are also mandated. The Act aims to prevent foodborne illness and improve traceback of contaminated products. It provides the FDA with new enforcement authorities while preserving its field laboratory infrastructure.
Introduction to Pharma regulatory affairs
Regulatory affairs is a profession that developed to oversee the regulation of products like pharmaceuticals, medical devices, and cosmetics by government agencies to ensure public health and safety. Regulatory affairs departments act as the interface between companies in regulated industries and regulatory agencies around the world. They track changing legislation, submit registration documents to agencies, and provide strategic and technical advice to other departments like R&D, manufacturing, and quality assurance.
Thailand Food Additives
By Chitra Settaudom, Senior Expert in Food Standards, Thaik Food & Drug Administration (date of publication unknown)
Spotless food-safety-standards-for-suppliers-issue-4
This document outlines Spotless' Food Safety Standard for Suppliers. It establishes Spotless' commitment to ensuring food and beverages purchased throughout the business are sourced from reputable suppliers that meet the requirements of Food Standards Australia New Zealand (FSANZ).
The standard applies to all Spotless approved food and beverage suppliers. It provides clear requirements for suppliers to meet based on the FSANZ Food Standards Code and state/territory food acts and regulations. Suppliers are expected to comply with the standard and will undergo inspections and audits by Spotless and approved certification agencies.
High, medium, and low risk suppliers will be categorized based on purchase groups and audited annually or biannually depending on
China new food safety law comprehensive compliance guidance part ii
This document summarizes the key impacts of China's new Food Safety Law on infant formula, health foods, and special dietary foods. It discusses increased regulations for infant formula, including whole process quality control, product registration, and restrictions on sub-packaging and using the same formula for different brands. It also outlines the import process for infant formula and challenges import companies may face, such as ensuring formulas are registered and formulations comply with local policies.
8_5x10-CDNReg
To legally sell dietary supplements, natural health products, foods, cosmetics, or over-the-counter drugs in Canada, various regulatory requirements must be met including obtaining licenses, submitting notifications, and ensuring label compliance. Quality Smart Solutions assists companies in navigating these regulations by reviewing product formulas and labels, preparing and submitting necessary license and notification applications to Health Canada, and providing importation services where required.
8. Feed/FSMA/FDA Update
The document provides an update on the Food Safety Modernization Act (FSMA). It summarizes key FSMA rules including current good manufacturing practice and preventive controls for animal and human food. It discusses FDA inspection activity and top citations. It outlines shipper responsibilities under the sanitary transportation rule and answers common questions about FSMA compliance. The document is intended to help grain and feed industry members understand FSMA requirements and FDA oversight activities.
Study of Marketing Conditions for Marketing Authorization of Over The Counter...
Study of Marketing Conditions for Marketing Authorization of Over The
Counter (OTC) and Homeopathic Products in US.
India Food Licensing & Registration: Impact to Industry
The document discusses the Food Safety and Standards Act (FSSA) 2006 and its impact on the food industry in India. It outlines some key issues with the previous multiplicity of food laws such as varied quality standards. It then summarizes some of the major features of the FSSA including provisions for licensing and registration, enforcement, adjudication, penalties, and regulations developed under the Act. Overall, the FSSA aims to establish a single reference point for all issues related to food safety and standards in India.
Regulatory opportunities for IP attorneys 2010
This document outlines topics related to compliance and intellectual property in the pharmaceutical industry. It discusses the FDA structure, drug development process, and key issues that affect IP lawyers, such as advertising, feedback loops during drug development, service agreements, drug naming, patent extensions and exclusivity, lifecycle management, and generic drug approval challenges. The document provides an overview of these topics at a high level and is intended to familiarize IP lawyers with compliance and regulatory considerations.
Rak presentation
The document discusses regulatory affairs and the regulatory environment in the Middle East pharmaceutical market. It provides an overview of regulatory affairs, the approval process for drugs, and highlights opportunities and challenges in major Middle Eastern markets like UAE, Saudi Arabia, and GCC countries. Regulations are evolving in the region and harmonizing with international standards to improve access to medicines while ensuring safety and efficacy.
The Food Safety Modernization Act
The recently enacted Food Safety Modernization Act is the greatest expansion of FDA’s food regulatory authority since the enactment in 1938 of the Federal Food, Drug, and Cosmetic Act. This presentation discuses the scope, impact and implementation of the Act. Presented by FDAImports.com Founder and CEO, Benjamin England.
For more on the Food Safety Modernization Act and how it affects companies, manufacturers and importers please visit:
http://www.fdaimports.com/FSMA
2011 GMA Conference: A Bit(e) of History
Food safety attorney Bill Marler's presentation at the 2011 Grocery Manufacturers Association Foodborne Illness Litigation Conference in Chicago in which he reviews the history of foodborne illness policy in the United States and how the culmination of numerous factors ultimately lead to the passage of The Food Safety Modernization Act in 2010.
More Related Content
What's hot
Fda
This document outlines the FDA's proposed plans and programs for regulating halal products in the Philippines. It discusses establishing a Halal Unit within the FDA to oversee licensing of halal establishments, registration of halal products, and post-market surveillance. Products that would be regulated include food, cosmetics, pharmaceuticals, and medical devices. The FDA plans to coordinate with other agencies like the NCMF and ensure its halal policies are consistent with national standards. Challenges include developing clear interagency policies and regulations on halal as well as expanding laboratory testing capabilities for halal products.
US FDA Regs & Modernization Act 2012
The document provides an overview of U.S. FDA regulations for exporting food and beverages to the U.S., including the Food Safety Modernization Act. It discusses the FDA's jurisdiction and structure, key food regulations on labeling, ingredients and claims. It also summarizes provisions of the FSMA relating to prevention of food hazards, mandatory inspections, import safety through programs like the Foreign Supplier Verification Program. The seminar aims to help exporters understand and comply with complex U.S. food safety rules.
Kerr, Jason Final Poster
Gilead Sciences prepares a Certificate of Pharmaceutical Product (CPP) application to submit to the FDA to export their drug Harvoni to Mongolia. A CPP provides essential information about a drug product for countries without strong regulatory systems. Gilead submits documentation about Harvoni's registration, formulation, labeling, and manufacturing to the FDA. If approved, the FDA issues an authenticated CPP valid for 24 months. Mongolia then reviews Gilead's drug application including the CPP to determine if Harvoni can be sold in their country. CPPs help ensure imported drugs meet good manufacturing practice standards and quality when countries lack regulatory capacity to verify this themselves.
FDA Export Certificates
Manufacturers that export FDA-regulated products such as drugs and medical devices from the US are oftentimes required to provide a certificate prepared by the FDA which confirms the product’s regulatory and marketing status...
AmCham Seminar
The document discusses new legislation and regulations around food safety in the United States. It outlines the Food Safety Modernization Act, which aims to modernize the food safety system by shifting from reactive to preventative response. Key points of the new law include increased mandatory inspections of domestic and foreign facilities by the FDA, requiring food safety plans and prevention controls, and more import certification requirements for foreign exporters. The changes are expected to significantly impact Chinese exporters through new registration, record access, inspection and food safety standard requirements.
DSHEA
1) The Dietary Supplement Health and Education Act of 1994 (DSHEA) defines and regulates dietary supplements in the US, placing them in the food category and requiring manufacturers to ensure safety and accurate labeling.
2) Use of dietary supplements increased after DSHEA, with over half of US adults regularly using supplements by 2003-2006, especially women.
3) DSHEA aimed to ensure continued consumer access to supplements while providing more information, without changing their status as foods regulated by FDA for safety.
Are you ready to implement FDA Food Safety Modernization Act?
The document discusses the Food Safety Modernization Act (FSMA), which establishes new rules for food safety in the United States. It was signed into law in 2011 to better protect public health by strengthening the food safety system from farm to table. The FSMA impacts farmers, food manufacturers, transporters, importers and others. Its major components establish requirements for preventive controls, inspections and compliance, imported food safety, and enhanced partnerships between food safety agencies. Compliance dates vary depending on business size, with larger businesses required to comply sooner.
Acheson / Bode Food Safety Law 01-06-11
The Food Safety Modernization Act grants the FDA new authorities to regulate food safety, including mandatory recall authority, expanded access to facility records, and increased oversight of imported foods. Key changes include increased inspection frequencies for domestic and foreign facilities based on risk factors. The FDA will also be able to require certification of imported foods by third-party auditors. Facilities that produce, process or distribute food will need to implement food safety plans and be prepared for greater regulatory scrutiny of their operations and records. The new law aims to shift the FDA's focus from response to prevention of foodborne illness outbreaks.
Avoiding Pitfalls in the Regulatory Path - MaRS Best Practices
Innovating in the life sciences and health-care sector? You can’t escape the regulators! Before you make a costly mistake, learn from the experts who have been through the process before.
Whether you’re working on a therapeutic, an in vitro diagnostic or a medical device, come find out how to identify and mitigate challenges along the path to regulatory approval.
FDA Globalization Act (Dingell Bill) Summary Jan 2009
The Food and Drug Administration Globalization Act of 2009 strengthens oversight of food, drug, medical device, and cosmetic safety. It requires facilities in the US and abroad to register annually with the FDA and pay fees to fund increased inspections. Safety plans and compliance with good manufacturing practices are also mandated. The Act aims to prevent foodborne illness and improve traceback of contaminated products. It provides the FDA with new enforcement authorities while preserving its field laboratory infrastructure.
Introduction to Pharma regulatory affairs
Regulatory affairs is a profession that developed to oversee the regulation of products like pharmaceuticals, medical devices, and cosmetics by government agencies to ensure public health and safety. Regulatory affairs departments act as the interface between companies in regulated industries and regulatory agencies around the world. They track changing legislation, submit registration documents to agencies, and provide strategic and technical advice to other departments like R&D, manufacturing, and quality assurance.
Thailand Food Additives
By Chitra Settaudom, Senior Expert in Food Standards, Thaik Food & Drug Administration (date of publication unknown)
Spotless food-safety-standards-for-suppliers-issue-4
This document outlines Spotless' Food Safety Standard for Suppliers. It establishes Spotless' commitment to ensuring food and beverages purchased throughout the business are sourced from reputable suppliers that meet the requirements of Food Standards Australia New Zealand (FSANZ).
The standard applies to all Spotless approved food and beverage suppliers. It provides clear requirements for suppliers to meet based on the FSANZ Food Standards Code and state/territory food acts and regulations. Suppliers are expected to comply with the standard and will undergo inspections and audits by Spotless and approved certification agencies.
High, medium, and low risk suppliers will be categorized based on purchase groups and audited annually or biannually depending on
China new food safety law comprehensive compliance guidance part ii
This document summarizes the key impacts of China's new Food Safety Law on infant formula, health foods, and special dietary foods. It discusses increased regulations for infant formula, including whole process quality control, product registration, and restrictions on sub-packaging and using the same formula for different brands. It also outlines the import process for infant formula and challenges import companies may face, such as ensuring formulas are registered and formulations comply with local policies.
8_5x10-CDNReg
To legally sell dietary supplements, natural health products, foods, cosmetics, or over-the-counter drugs in Canada, various regulatory requirements must be met including obtaining licenses, submitting notifications, and ensuring label compliance. Quality Smart Solutions assists companies in navigating these regulations by reviewing product formulas and labels, preparing and submitting necessary license and notification applications to Health Canada, and providing importation services where required.
8. Feed/FSMA/FDA Update
The document provides an update on the Food Safety Modernization Act (FSMA). It summarizes key FSMA rules including current good manufacturing practice and preventive controls for animal and human food. It discusses FDA inspection activity and top citations. It outlines shipper responsibilities under the sanitary transportation rule and answers common questions about FSMA compliance. The document is intended to help grain and feed industry members understand FSMA requirements and FDA oversight activities.
Study of Marketing Conditions for Marketing Authorization of Over The Counter...
Study of Marketing Conditions for Marketing Authorization of Over The
Counter (OTC) and Homeopathic Products in US.
India Food Licensing & Registration: Impact to Industry
The document discusses the Food Safety and Standards Act (FSSA) 2006 and its impact on the food industry in India. It outlines some key issues with the previous multiplicity of food laws such as varied quality standards. It then summarizes some of the major features of the FSSA including provisions for licensing and registration, enforcement, adjudication, penalties, and regulations developed under the Act. Overall, the FSSA aims to establish a single reference point for all issues related to food safety and standards in India.
Regulatory opportunities for IP attorneys 2010
This document outlines topics related to compliance and intellectual property in the pharmaceutical industry. It discusses the FDA structure, drug development process, and key issues that affect IP lawyers, such as advertising, feedback loops during drug development, service agreements, drug naming, patent extensions and exclusivity, lifecycle management, and generic drug approval challenges. The document provides an overview of these topics at a high level and is intended to familiarize IP lawyers with compliance and regulatory considerations.
Rak presentation
The document discusses regulatory affairs and the regulatory environment in the Middle East pharmaceutical market. It provides an overview of regulatory affairs, the approval process for drugs, and highlights opportunities and challenges in major Middle Eastern markets like UAE, Saudi Arabia, and GCC countries. Regulations are evolving in the region and harmonizing with international standards to improve access to medicines while ensuring safety and efficacy.
What's hot (20)
Are you ready to implement FDA Food Safety Modernization Act?
Are you ready to implement FDA Food Safety Modernization Act?
Avoiding Pitfalls in the Regulatory Path - MaRS Best Practices
Avoiding Pitfalls in the Regulatory Path - MaRS Best Practices
FDA Globalization Act (Dingell Bill) Summary Jan 2009
FDA Globalization Act (Dingell Bill) Summary Jan 2009
Spotless food-safety-standards-for-suppliers-issue-4
Spotless food-safety-standards-for-suppliers-issue-4
China new food safety law comprehensive compliance guidance part ii
China new food safety law comprehensive compliance guidance part ii
Study of Marketing Conditions for Marketing Authorization of Over The Counter...
Study of Marketing Conditions for Marketing Authorization of Over The Counter...
India Food Licensing & Registration: Impact to Industry
India Food Licensing & Registration: Impact to Industry
Viewers also liked
The Food Safety Modernization Act
The recently enacted Food Safety Modernization Act is the greatest expansion of FDA’s food regulatory authority since the enactment in 1938 of the Federal Food, Drug, and Cosmetic Act. This presentation discuses the scope, impact and implementation of the Act. Presented by FDAImports.com Founder and CEO, Benjamin England.
For more on the Food Safety Modernization Act and how it affects companies, manufacturers and importers please visit:
http://www.fdaimports.com/FSMA
2011 GMA Conference: A Bit(e) of History
Food safety attorney Bill Marler's presentation at the 2011 Grocery Manufacturers Association Foodborne Illness Litigation Conference in Chicago in which he reviews the history of foodborne illness policy in the United States and how the culmination of numerous factors ultimately lead to the passage of The Food Safety Modernization Act in 2010.
Foreign Supplier Verification Programs [FSVP]
Under Food Safety modernization Act (FSMA) Food and Drug Administration (FDA) issued final rule for Foreign Supplier Verification Programs (FSVP) on November 13, 2015
Foreign Supplier Verification Programs (FSVP) applies to all imported food, beverages, and dietary supplements/ingredients unless the importer or foreign supplier is exempted by FSMA, or it the food is under the exclusive jurisdiction of USDA.
FSVP Rule requires importers to share responsibility for ensuring safety of imported product!
“Importer” is U.S. owner or consignee of a food at time of U.S. entry.
If no U.S. owner or consignee at entry, importer is U.S. agent or representative of the foreign owner or consignee, as confirmed in signed statement of consent.
Mo agri business marketing forum
The document discusses the benefits of exporting for agricultural businesses. It outlines how exporting can increase sales and income by accessing the 95% of consumers living outside the US. Exporting also helps diversify markets and offsets domestic demand fluctuations. The Food Export Association of the Midwest promotes exports of Midwestern food products. It partners with USDA agencies and state organizations to help small and medium companies enter new markets through programs providing education, market intelligence, trade missions and reimbursements for branded product promotions overseas.
Food safety us
The document discusses Ontario's Food Safety Modernization Act and the impact of food recalls in the US and Canada. It proposes creating a private-public partnership to implement a new approach and disruptive technology using RFID, barcodes, and geomapping to track food through the supply chain in real-time. This would empower consumers, producers and the government to contain product failures. It suggests forming a working group to develop a software pilot program to propose to the Ontario Ministry of Agriculture for $1 million.
Food Safety Modernization Act Webinar
A webinar presented by the Food & Beverage Industry Alliance, covering the legal, IT and business perspectives of the FDA's Food Safety Modernization Act
Food Safety Modernization Act: What Does It Mean For Importers?
Learn the new regulations for food safety import. Understand how FSMA requires importers to conduct risk-based preventive controls and verification activities.
Food Safety Modernization Act
The document provides an overview of a presentation about the Food Safety Modernization Act. It discusses the impetus for the act due to health risks from foodborne illness. It outlines key provisions such as requiring food facilities to evaluate hazards and have preventative control plans, increasing traceability and inspection requirements, and giving FDA mandatory recall authority. It also discusses how an ERP system called S2K Enterprise can help companies comply with the new regulations through features like import tracking, lot control, quality testing, and recall reporting.
U.S. Food Safety Modernization Act: A Primer
The first overhaul of the U.S. food manufacturing process in more than 80 years, the federal Food Safety Modernization Act (FSMA) law updates the role of the government in verifying the safety and availability of our food supply. FSMA, as it rolls out, has implications for both domestic manufacturers and those that distribute goods made abroad, in foreign facilities. The Food Institute analyzed the intersection of daily food production and regulatory compliance in this first in a series of 3 presentations on FSMA.
USA Sanitary Food Transportation Act
The Food Safety Modernization Act (FSMA) includes changes related to sanitary transportation that will affect retailers and wholesalers with distribution centers; and retailers and wholesalers with distribution centers and truck fleets. This is the first time FDA has proposed comprehensive rules related to transportation so the proposed changes impose significant new requirements for food retailers.
For example, FDA includes requirements related to the design and maintenance of vehicles and transportation equipment to ensure that it does not cause the food that it transports to become contaminated. (Reference: Stephanie Barnes, Regulatory Counsel, Food Marketing Institute)
Food Safety Modernization Act: for importers
The Food Safety Modernization Act is the largest overhaul of the U.S. food processing system in more than 80 years. Thought it impacts domestic and foreign producers, there are quite a few changes in the new law important for Importers & foreign food manufacturers. Here is a highlight on how FSMA impacts Imported foods.
2016 Business of Farming Conference: FDA Food Safety Modernization Act Produc...
The document discusses the FDA Food Safety Modernization Act Produce Rule and how it will affect farms. It provides information on:
- Coverage of the rule, including which farms and produce are covered based on factors like annual produce sales and whether produce is eaten raw.
- Key requirements of the rule for covered farms, including requirements around agricultural water and biological soil amendments.
- Exemptions from parts of the rule for qualified exempt farms that meet sales thresholds for direct consumer sales within a certain distance. Requirements for exempt farms include recordkeeping, labeling and annual reviews.
Infusionsoft Lifecycle Marketing
This document discusses how Infusionsoft helps small businesses succeed through lifecycle marketing. It begins by introducing Ramon Ray and Infusionsoft. It then discusses how many small businesses fail due to using disjointed, survival-based marketing tactics. In contrast, lifecycle marketing focuses on treating leads and customers like individuals through targeted, relationship-based communications. This approach helps small businesses attract more visitors, capture more leads, nurture prospects, increase sales and customer satisfaction.
Interpretation of Administrative Measure on Health Food Registration Filing, ...
Interpretation of Administrative Measure on Health Food Registration Filing, ...Asian Food Regulation Information Service
This document provides an overview of health food regulations in China. It discusses the key definitions and classifications of health foods, the major regulations governing health foods, and the processes for registration and filing of health foods. It also describes the document requirements, testing scopes, and differences between registration and filing. Registration involves more extensive dossier requirements, testing, and a longer timeline than filing. The document aims to help companies understand the regulatory landscape for placing health foods in the Chinese market.How to Successfully Import Natural Products to the USA
How to import natural and organic products to the United States.
• Foods and Dietary Supplements
• How FDA, USDA and Customs interact
• Import Compliance
• Import Alerts and FDA detentions
• Organic and Natural claims
• Food Safety Modernization Act
Originally presented by Rick Quinn, Principal, at the 2012 Natural Products Expo Asia in Hong Kong.
© 2012 FDAImports.com and ExportToUsa.com.cn
http://www.fdaimports.com
http://www.exporttousa.com.cn
Viewers also liked (15)
Food Safety Modernization Act: What Does It Mean For Importers?
Food Safety Modernization Act: What Does It Mean For Importers?
2016 Business of Farming Conference: FDA Food Safety Modernization Act Produc...
2016 Business of Farming Conference: FDA Food Safety Modernization Act Produc...
Interpretation of Administrative Measure on Health Food Registration Filing, ...
Interpretation of Administrative Measure on Health Food Registration Filing, ...
How to Successfully Import Natural Products to the USA
How to Successfully Import Natural Products to the USA
Similar to 10 Steps To Import Seafood Into the United States From China 进口水产品到美国的十大步骤： FDA进口检验流程
FDA & Health Canada (CFIA) Requirements to Sell Foods in North America
This food compliance webinar focuses on food labelling requirements, TMAL, requirements to import or export food. U.S Agent, FSVP agent and more.
Visit:
https://qualitysmartsolutions.com/food-beverage-regulatory-compliance-canada/
https://qualitysmartsolutions.com/food-beverage-regulatory-compliance-canada/
Mas Hori Presentation at FDA LOS
Regulatory audits enforce food safety regulations and ensure compliance, while customer-driven audits are conducted by third parties to meet customer requirements. Regulatory audits require more documentation and adherence to preventive controls, HACCP, SSOP, and GMP regulations. Customer audits also require documentation of food safety programs but may not require all the same preventive controls and hazard analyses as regulatory audits. Food companies will need both types of audits to comply with regulations and meet customer food safety standards.
FSMA Requirements For Exporting Food to the United States
What are the FSMA rules, how does FSMA affect foreign food facilities, and what are the FDA requirements for food export?
Trust, but Verify - Tips & Tools for FSMA's Foreign Supplier Verification
The FDA’s Food Safety Modernization Act (FSMA) rule on Foreign Supplier Verification Programs (FSVP) for Importers of Food for Humans and Animals is now final, and compliance dates for some businesses begin in 18 months. To help the food supply chain prepare, TraceGains’ will zero-in on the FSVP in its upcoming webinar: “Trust, but Verify – Tips and Tools for Foreign Supplier Verification (FSV).”
TraceGains will host FDA attorney Marc Sanchez as its guest speaker for the webinar. The session is designed to give an overview of the key provisions and tips and tools you can use to simplify compliance with the new requirements and establish a world-class FSVP.
Specifically, the webinar will cover:
Examining your current supplier program and how to identify gaps in hazard analysis;
What the FDA says about electronic record-keeping for FSV;
What involvement is expected from the executive and management level;
Third-party verification of foreign suppliers;
Risk management best practices for FSV; and,
Tips & tools to simplify compliance with FSV.
Us food safety systems
The document provides background information on the U.S. food safety system. It discusses the main federal regulatory agencies that oversee food safety - the USDA and FDA. The USDA regulates meat and poultry products while the FDA regulates all other foods, including imports. Other agencies like CDC and EPA also play roles. The agencies have different statutory authorities that influence their oversight approaches. The U.S. system relies on cooperation between federal, state, and local authorities.
Safe Food for Canadians Regulations (SFCR)
Safe Food for Canadians Regulation – Are You Ready?
The Safe Food Canadians Act is a bit of a ‘sleeping’ giant, as the regulations came into effect January 15, 2019. Many food companies both within Canada and outside its borders are still trying to figure out what they need to do in order to comply.
This informative webinar featuring Cameron Prince with The Acheson Group discusses:
- Top 3 pillars of the Safe Food Canadians Regulations and how they compare to FSMA
- What companies should have in place, or work towards quickly, to ensure compliance – relative to licensing, traceability and preventive controls
- The long term impact these regulations will have on food companies, and predictions on enforcement
Learn more at https://safetychain.com
Safe Food for Canadians Regulation (SFCR) - Are You Ready?
This document provides an overview and summary of Canada's new Safe Food for Canadians Regulation (SFCR) which comes into effect on January 15, 2019. It outlines the key elements of the new regulation including licensing requirements, preventive control measures, traceability rules, and the steps companies need to take to transition. The regulation aims to modernize and consolidate Canada's food safety rules and better protect consumers from foodborne illness.
Food Importers Have a Special Requirment that Must be Met.
The FDA's Foreign Supplier Verification Program (FSVP) requires US companies importing food to designate a US representative to maintain supply chain records. FSVP applies to facilities manufacturing, processing, packing, or holding food for human or animal consumption in the US, except for certain regulated foods like seafood and juice. Janel helps clients identify FSVP compliance responsibilities and create strategies to meet them, offering assistance from their Director of Compliance.
Driving Profitable Growth Despite All the Landmines in the Food & Beverage In...
Webinar presented by the Food & Beverage Industry Alliance
- How to navigate the complex regulatory environment
- How to stand out in today's crowded marketplace
- How to use Business Intelligence Systems to make superior decisions to drive growth and profitability
-
Attend the Industry’s Premier Legal, Regulatory & Compliance Dietary Suppleme...
Attend the Industry’s Premier Legal, Regulatory & Compliance Dietary Suppleme...American Conference Institute
American Conference Institute (ACI) in collaboration with the Council for Responsible Nutrition (CRN) is pleased to present ACI’s 4th annual Legal, Regulatory, and Compliance Forum on Dietary Supplements.Health Canada Compliance Solution | FDA Compliance Solution
Are you searching for a Regulatory Compliance Consultant that can help you acquire a Natural Product Number (NPN) for your NHP product? If so, Quality Smart Solutions is the right place. QSS is a renowned global consulting firm with a successful track record of registering more than 5,000 NPNs since inception. This company helps meet compliant bilingual label requirements and an Importer of Recorder. Get assistance in preparing a Product license application (PLA), Electronic Product License Application (ePLA) for a class 1 or 2 NHP, Electronic Product License Application for a class 3 NHP, an Evidence Summary Report (it includes information for safety and efficacy support) and a finished product specification form.
For more information about Regulatory Compliance Service at Quality Smart Solutions, visit the official website https://qualitysmartsolutions.com/.
Good clinical practices tutorial- v7.015--shehnaz_june-10_v 3.0
- The document discusses regulatory issues related to conducting clinical trials in India, including the regulatory framework, applicable local regulations, advantages of conducting trials in India, and key challenges.
- Some advantages include reasonable regulatory approvals, high incidence of diseases common in Western countries, large treatment-naïve populations, and English as the primary business language.
- However, challenges include a shortage of GCP-trained investigators, documentation practices like back-dating records, busy investigator schedules, and variable infrastructure across sites.
Imminent Labeling Changes: A TraceGains Webinar with Food Directions
If you have any questions or comments, please send them to connect@tracegains.com. We look forward to hearing from you.
Meeting Description:
Consumers are often confused by food labels. Yet the entire food production industry is facing proposed labeling changes that can affect packaging design, ingredient choices, sourcing decisions, and so on. Many of these pending requirements could add even more confusion in the consumer marketplace.
Join us for a webinar with food policy expert Beth Johnson, MS, RD, founder and principal of Food Directions LLC, a boutique government relations firm headquartered in Washington, D.C. Johnson will discuss imminent labeling initiatives including:
-Genetically modified organism labeling debates
-Nutrition facts panel reform
-Gluten free labeling
-Menu and vending labeling
Learn what your company or organization can anticipate in terms of content and timing and how it can begin to prepare for the many changes ahead.
About Food Directions:
Food Directions operates at the intersection where public affairs meets food policy. With a thorough understanding of the interconnectedness of the legislative and regulatory process, Food Directions follows all issues related to agriculture, food safety, and nutrition policy at the federal, state, and international level. Headquartered in Washington, with deep relationships within federal agencies like Food and Drug Administration (FDA) and United States Department of Agriculture (USDA), and on Capitol Hill, Food Directions is plugged into the ever-changing dynamic.
Fda gmp compliance for the Life Science Industry
The document discusses good manufacturing practices (GMP) required by the FDA for life science companies. It provides an overview of GMP regulations for drugs, medical devices, and combination products. It explains that the FDA focuses on a "state of control" during inspections to assess compliance. While drug GMPs and device quality system regulations differ in some details, the overall systems are similar. The document reviews how the regulations address statistical techniques and quality systems. It also outlines the FDA's systems-based approach to inspections.
Losses due non-compliance with China food regulation and how to overcome Chi...
As the world’s largest imported food market, China imported totally 38 billion US dollars food products from187 countries in 2016.
The growing China market has attracted a lot of interest from different countries over the world. Meanwhile China government has, over the last years, developed a tougher and tougher food regulation regime to regulate the market and ensure food safety.
Due to various challenges (languages, resources, information accessibility etc.), foreign SMEs learned a lot lessons and experienced big losses due to non-compliance with Chinese regulations.
Actually majority of these losses due non-compliance can be easily prevented if SMEs have reliable regulatory information in hand.
As a leading Chinese food regulation consulting company, FoodMate developed “Compliance Excellence” information service product for foreign SMEs with target to minimize your losses due regulatory non-compliance by assessing reliable and tailor made regulatory information.
FDA Enforcement: The Cop is Back – How Enhanced Enforcement Can Impact You a...
December 15, 2010 webinar sponsored by The Weinberg Group on increased FDA enforcement activity under the Obama administration, with a focus on:
Enforcement Trends Prior to Obama Administration
Commissioner Hamburg Revives FDA’s Compliance Culture –The August 6, 2009 Speech and its Impact
Key FDA Enforcement Actions
How to Prepare for Increased Enforcement
How to Respond if Targeted
Consequences of Non-Compliance
FDA’s Record under Enhanced Compliance
Proactive FSMA Compliance: What 2022 Taught Us to Better Plan Ahead
With the second half of 2022 before us, we will look back at how food manufacturers navigated recent shifts in FDA requirements to help better prepare for compliance deadlines later this year.
Join Eric Edmunds, Food Safety Director at The Acheson Group, as he walks through FDA enforcement discretion for labeling issues caused by supply chain disruptions and new FDA sesame declaration requirements, how the FDA is enforcing FSVP after COVID, what food manufacturers can learn from the recent Delta 8 ruling impacting the 2018 Farm Bill, and how to become more “recall ready” in line with FDA’s recent guidance for voluntary recalls.
Implementation of GMP’s for Cosmetics in a Changing Global Environment Traini...
Implementation of GMP’s for Cosmetics in a Changing Global Environment Traini...Atlantic Training, LLC.
This document provides an overview of GMP regulations for cosmetics in the US, EU, and ASEAN regions. It discusses key aspects of GMPs including quality systems, standard operating procedures, production processes, equipment cleaning, quality control testing, and auditing. The goals of GMPs are to prevent contamination and errors, ensure product quality and safety, and comply with various regulatory requirements for cosmetics. While the US does not have explicit GMP regulations for cosmetics, the FDA provides GMP guidelines and can take action if a product is deemed adulterated or misbranded.FSMA FOR US IMPORTERS OF CHINESE FOOD
The document discusses how the Food Safety Modernization Act (FSMA) will affect food imports from China into the US. Some key ways include:
1) Requiring importers to verify that foreign suppliers, including those in China, comply with new food safety standards through a Foreign Supplier Verification Program.
2) Subjecting high-risk foods from China to new import certification requirements.
3) Providing a voluntary program for qualified importers to expedite food imports, but this will require third-party certifications showing compliance with FSMA standards.
4) Increasing the number of FDA inspections of foreign food facilities, including in China, and allowing FDA to deny imports from facilities that
Process guidelines for foreign companies exporting infant formula to China
As a leading China food regulation consulting company, FoodMate developed this report to outline challenges for foreign companies exporting product to China. An in depth regulation mapping and step by step compliance guideline of exporting infant formula to China is also interpreted in this report.
Similar to 10 Steps To Import Seafood Into the United States From China 进口水产品到美国的十大步骤： FDA进口检验流程 (20)
FDA & Health Canada (CFIA) Requirements to Sell Foods in North America
FDA & Health Canada (CFIA) Requirements to Sell Foods in North America
FSMA Requirements For Exporting Food to the United States
FSMA Requirements For Exporting Food to the United States
Trust, but Verify - Tips & Tools for FSMA's Foreign Supplier Verification
Trust, but Verify - Tips & Tools for FSMA's Foreign Supplier Verification
Safe Food for Canadians Regulation (SFCR) - Are You Ready?
Safe Food for Canadians Regulation (SFCR) - Are You Ready?
Food Importers Have a Special Requirment that Must be Met.
Food Importers Have a Special Requirment that Must be Met.
Driving Profitable Growth Despite All the Landmines in the Food & Beverage In...
Driving Profitable Growth Despite All the Landmines in the Food & Beverage In...
Attend the Industry’s Premier Legal, Regulatory & Compliance Dietary Suppleme...
Attend the Industry’s Premier Legal, Regulatory & Compliance Dietary Suppleme...
Health Canada Compliance Solution | FDA Compliance Solution
Health Canada Compliance Solution | FDA Compliance Solution
Good clinical practices tutorial- v7.015--shehnaz_june-10_v 3.0
Good clinical practices tutorial- v7.015--shehnaz_june-10_v 3.0
Imminent Labeling Changes: A TraceGains Webinar with Food Directions
Imminent Labeling Changes: A TraceGains Webinar with Food Directions
Losses due non-compliance with China food regulation and how to overcome Chi...
Losses due non-compliance with China food regulation and how to overcome Chi...
FDA Enforcement: The Cop is Back – How Enhanced Enforcement Can Impact You a...
FDA Enforcement: The Cop is Back – How Enhanced Enforcement Can Impact You a...
Proactive FSMA Compliance: What 2022 Taught Us to Better Plan Ahead
Proactive FSMA Compliance: What 2022 Taught Us to Better Plan Ahead
Implementation of GMP’s for Cosmetics in a Changing Global Environment Traini...
Implementation of GMP’s for Cosmetics in a Changing Global Environment Traini...
Process guidelines for foreign companies exporting infant formula to China
Process guidelines for foreign companies exporting infant formula to China
Recently uploaded
Kirill Klip GEM Royalty TNR Gold Lithium Presentation
Lithium Will Power Us For The Next 50 Years And Then Robots: Kirill Klip GEM Royalty TNR Gold Lithium Presentation
Prescriptive analytics BA4206 Anna University PPT
Business analysis - Prescriptive analytics Introduction to Prescriptive analytics
Prescriptive Modeling
Non Linear Optimization
Demonstrating Business Performance Improvement
一比一原版(QMUE毕业证书)英国爱丁堡玛格丽特女王大学毕业证文凭如何办理
永久可查学历认证【微信：A575476】【(QMUE毕业证书)英国爱丁堡玛格丽特女王大学毕业证成绩单Offer】【微信：A575476】（留信学历认证永久存档查询）采用学校原版纸张、特殊工艺完全按照原版一比一制作（包括：隐形水印，阴影底纹，钢印LOGO烫金烫银，LOGO烫金烫银复合重叠，文字图案浮雕，激光镭射，紫外荧光，温感，复印防伪）行业标杆！精益求精，诚心合作，真诚制作！多年品质 ,按需精细制作，24小时接单,全套进口原装设备，十五年致力于帮助留学生解决难题，业务范围有加拿大、英国、澳洲、韩国、美国、新加坡，新西兰等学历材料，包您满意。
【业务选择办理准则】
一、工作未确定，回国需先给父母、亲戚朋友看下文凭的情况，办理一份就读学校的毕业证【微信：A575476】文凭即可
二、回国进私企、外企、自己做生意的情况，这些单位是不查询毕业证真伪的，而且国内没有渠道去查询国外文凭的真假，也不需要提供真实教育部认证。鉴于此，办理一份毕业证【微信：A575476】即可
三、进国企，银行，事业单位，考公务员等等，这些单位是必需要提供真实教育部认证的，办理教育部认证所需资料众多且烦琐，所有材料您都必须提供原件，我们凭借丰富的经验，快捷的绿色通道帮您快速整合材料，让您少走弯路。
留信网认证的作用:
1:该专业认证可证明留学生真实身份
2:同时对留学生所学专业登记给予评定
3:国家专业人才认证中心颁发入库证书
4:这个认证书并且可以归档倒地方
5:凡事获得留信网入网的信息将会逐步更新到个人身份内，将在公安局网内查询个人身份证信息后，同步读取人才网入库信息
6:个人职称评审加20分
7:个人信誉贷款加10分
8:在国家人才网主办的国家网络招聘大会中纳入资料，供国家高端企业选择人才
→ 【关于价格问题（保证一手价格）
我们所定的价格是非常合理的，而且我们现在做得单子大多数都是代理和回头客户介绍的所以一般现在有新的单子 我给客户的都是第一手的代理价格，因为我想坦诚对待大家 不想跟大家在价格方面浪费时间
对于老客户或者被老客户介绍过来的朋友，我们都会适当给一些优惠。
选择实体注册公司办理，更放心，更安全！我们的承诺：可来公司面谈，可签订合同，会陪同客户一起到教育部认证窗口递交认证材料，客户在教育部官方认证查询网站查询到认证通过结果后付款，不成功不收费！
Dpboss Matka Guessing Satta Matta Matka Kalyan Chart Indian Matka
Dpboss Matka Guessing Satta Matta Matka Kalyan Chart Indian Matka➒➌➎➏➑➐➋➑➐➐Dpboss Matka Guessing Satta Matka Kalyan Chart Indian Matka
9356872877Sattamatka.satta.matka.satta matka.kalyan weekly chart.kalyan chart.kalyan jodi chart.kalyan penal chart.kalyan today.kalyan open.fix satta.fix fix fix Satta matka nambar.Kirill Klip GEM Royalty TNR Gold Copper Presentation
Tesla Energy rEVolution And The Golden Age For Copper: Kirill Klip GEM Royalty TNR Gold Copper Presentation
AI Transformation Playbook: Thinking AI-First for Your Business
I dive into how businesses can stay competitive by integrating AI into their core processes. From identifying the right approach to building collaborative teams and recognizing common pitfalls, this guide has got you covered. AI transformation is a journey, and this playbook is here to help you navigate it successfully.
IMG_20240615_091110.pdf dpboss guessing
Satta matka fixx jodi panna all market dpboss matka guessing fixx panna jodi kalyan and all market game liss cover now 420 matka office mumbai maharashtra india fixx jodi panna
Call me 9040963354
WhatsApp 9040963354
Satta Matka Dpboss Kalyan Matka Results 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 KALYAN CHART
欧洲杯投注-欧洲杯投注外围盘口-欧洲杯投注盘口app|【网址🎉ac22.net🎉】
【网址🎉ac22.net🎉】欧洲杯投注是体育博彩和在线赌场之一，得益于UKGC的三项许可。 成立之初是三名博彩公司将40家博彩商店的合并的结果，共同创建一家名为欧洲杯投注的公司。 欧洲杯投注在线赌场为游戏爱好者提供了300多种游戏，其中200多种老虎机，其他游戏包括二十一点，轮盘，真人荷官和真人赌场等。
Satta Matka Dpboss 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
欧洲杯赌球-欧洲杯赌球买球官方官网-欧洲杯赌球比赛投注官网|【网址🎉ac55.net🎉】
【网址🎉ac55.net🎉】欧洲杯赌球是世界上历史最悠久的博彩公司之一。其历史可以追溯到十九世纪末，确切时间是1886年。这家英国公司拥有超过15000名员工，是博彩行业规模最大的公司。欧洲杯赌球是英国最受欢迎的实体博彩公司之一，其排名仅次于欧洲杯赌球，旗下2800家投注站遍布全英国。
Discover the Beauty and Functionality of The Expert Remodeling Service
Unlock your kitchen's true potential with expert remodeling services from O'Brien Group Inc. Transform your space into a functional, modern, and luxurious haven with their experienced professionals. From layout reconfiguration to high-end upgrades, they deliver stunning results tailored to your style and needs. Visit obriengroupinc.com to elevate your kitchen's beauty and functionality today.
Satta Matka Dpboss 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 INDIA MATKA KALYAN SATTA MATKA 420 INDIAN MATKA SATTA KING MATKA FIX JODI FIX FIX FIX SATTA NAMBAR MATKA INDIA SATTA BATTA
Best Competitive Marble Pricing in Dubai - ☎ 9928909666
Stone Art Hub offers the best competitive Marble Pricing in Dubai, ensuring affordability without compromising quality. With a wide range of exquisite marble options to choose from, you can enhance your spaces with elegance and sophistication. For inquiries or orders, contact us at ☎ 9928909666. Experience luxury at unbeatable prices.
Sustainable Logistics for Cost Reduction_ IPLTech Electric's Eco-Friendly Tra...
Sustainable Logistics for Cost Reduction_ IPLTech Electric's Eco-Friendly Transport Solution
Adani Group's Active Interest In Increasing Its Presence in the Cement Manufa...
Time and again, the business group has taken up new business ventures, each of which has allowed it to expand its horizons further and reach new heights. Even amidst the Adani CBI Investigation, the firm has always focused on improving its cement business.
8328958814KALYAN MATKA | MATKA RESULT | KALYAN
8328958814KALYAN MATKA | MATKA RESULT | KALYAN KALYAN MATKA | MATKA RESULT | KALYAN MATKA TIPS | SATTA MATKA | MATKA.COM | MATKA PANA
Recently uploaded (20)
Kirill Klip GEM Royalty TNR Gold Lithium Presentation
Kirill Klip GEM Royalty TNR Gold Lithium Presentation
Dpboss Matka Guessing Satta Matta Matka Kalyan Chart Indian Matka
Dpboss Matka Guessing Satta Matta Matka Kalyan Chart Indian Matka
Kirill Klip GEM Royalty TNR Gold Copper Presentation
Kirill Klip GEM Royalty TNR Gold Copper Presentation
AI Transformation Playbook: Thinking AI-First for Your Business
AI Transformation Playbook: Thinking AI-First for Your Business
Satta Matka Dpboss Kalyan Matka Results Kalyan Chart
Satta Matka Dpboss Kalyan Matka Results Kalyan Chart
Satta Matka Dpboss Kalyan Matka Results Kalyan Chart
Satta Matka Dpboss Kalyan Matka Results Kalyan Chart
Discover the Beauty and Functionality of The Expert Remodeling Service
Discover the Beauty and Functionality of The Expert Remodeling Service
Satta Matka Dpboss Kalyan Matka Results Kalyan Chart
Satta Matka Dpboss Kalyan Matka Results Kalyan Chart
Best Competitive Marble Pricing in Dubai - ☎ 9928909666
Best Competitive Marble Pricing in Dubai - ☎ 9928909666
Sustainable Logistics for Cost Reduction_ IPLTech Electric's Eco-Friendly Tra...
Sustainable Logistics for Cost Reduction_ IPLTech Electric's Eco-Friendly Tra...
Adani Group's Active Interest In Increasing Its Presence in the Cement Manufa...
Adani Group's Active Interest In Increasing Its Presence in the Cement Manufa...
10 Steps To Import Seafood Into the United States From China 进口水产品到美国的十大步骤： FDA进口检验流程
- 1. 10 Steps to Import Seafood Into the United States: FDA Import Procedures 进口水产品到美国的十大步骤： FDA 进口检验流程 PRESENTED BY: RICK D. QUINN, ESQ. Senior Associate Attorney, FDAImports.com & ExportToUsa.com.cn 昆天佑。
- 3. 1. Facility Registration and U.S. Agency • U.S. Agency and Food Facility Registration: Requirements • New Obligations Under FDA Food Safety Modernization Act • Consequences of Improper Registration 设施注册及美国相关政府单位 美国政府对食品产销企业注册有哪些法规要求 在新的食品安全现代化法规里有什么新要求 如果没有办好食品设施注册会有什么后果
- 4. 2. Prior Notice and Food Facility Verification • Prior Notice and Food Facility Verification Requirement • When to Comply • What are the Consequences of a Failure to Comply 预先通知及食品设施查证 预先通知及食品设施查证有哪些法规要求 何时需要完成法规要求 如果不能达成法规要求会有什么后果
- 13. Questions & Answers 问题与解答
- 14. www.ExportToUsa.com.cn www.FDAImports.com PRESENTED BY: RICK D. QUINN, ESQ. Senior Associate Attorney, FDAImports.com & ExportToUsa.com.cn 昆天佑。