5263 UPC CERTIFICATE
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IAPMO Research and Testing, Inc. tests samples of fill valves from Xiamen Vib Industry & Trade Co., Ltd. to verify compliance with plumbing codes and standards. They also inspect the factory and quality assurance system through periodic surveillance. This listing certificate is valid from June 2015 through June 2016 and certifies that the listed fill valve models comply with standards for anti-siphon devices and can be installed according to code. The listing is contingent upon the company maintaining the same material, design, and quality standards and is not a guarantee of acceptance by local authorities.
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5264 UPC CERTIFICATE
IAPMO Research and Testing, Inc. tests samples of flush valves with dual flush devices from Xiamen Vib Industry & Trade Co., Ltd. to verify compliance with plumbing codes and standards. IAPMO conducts periodic inspections of the factory and assesses the quality assurance system. This listing confirms the products meet requirements but does not guarantee acceptance by local authorities. The listing is valid until June 2016 and may be revoked if the product design, manufacturing, or compliance changes without approval.
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5264 UPC CERTIFICATE
IAPMO Research and Testing, Inc. tests samples of flush valves with dual flush devices from Xiamen Vib Industry & Trade Co., Ltd. to verify compliance with plumbing codes and standards. IAPMO conducts periodic inspections of the factory and assesses the quality assurance system. This listing confirms the products meet requirements but does not guarantee acceptance by local authorities. The listing is valid until June 2016 and may be revoked if the product design, manufacturing, or compliance changes without approval.
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Ccc工厂检查简介
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systems – Requirements for regulatory
Purposes. ISO is an organization that develops Standards for use
worldwide.
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consumers and users of medical devices.
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Management System (QMS).
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• Set Quality goals
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- The registration process involves documentation, sample testing, and obtaining a unique registration number from BIS. Products must display the BIS mark and comply with labeling requirements.
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This certificate certifies that B-F Mold Technology Co., Ltd. has a quality management system that complies with the ISO 9001:2008 standard. The certificate is valid from December 9, 2016 to September 14, 2018 for plastic production, plastic mold, die casting mold, and stamping mold making. The certificate must be maintained through periodic surveillance audits by Beijing Zhongding Hengchang Certification Co., Ltd. and is invalid if assessments are overdue.
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2. New standards specify that laboratories must be committed to impartiality and minimize risks to impartiality. Personnel must keep information confidential, unless legally required. Laboratories must define their organizational structure and personnel responsibilities.
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This document provides information on various pharmaceutical certification systems including WHO-GMP, ISO 9000, ISO 14000, and the WHO certification scheme. It explains that GMP certification focuses on consistent production of quality products according to standards, while ISO 9000 certification focuses on quality management across an organization. ISO 14000 provides environmental management standards. The WHO certification scheme facilitates international trade of pharmaceuticals between countries by issuing certificates for products, licensing status, and batches. Overall the document gives an overview of important certification systems for the pharmaceutical industry.
Auditing of vendors and production department
The document discusses vendor audits in the pharmaceutical industry. It provides details on the objectives, parameters, and steps of conducting a vendor audit. The key points are:
- Vendor audits assess a vendor's quality management system, practices, documentation, and adherence to standards to ensure their products and services meet requirements.
- Important parameters reviewed include ISO certifications, manufacturing facilities, packaging and labeling standards, and data handling procedures.
- The goals are to evaluate quality control measures and management commitment to quality standards required by regulations.
- Conducting vendor audits helps reduce costs and risks by gaining insight into supplier processes and compliance.
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This document provides information on pilot plants and scale-up in the pharmaceutical industry. It defines pilot plants as where lab-scale formulas are transformed into viable products through reliable manufacturing procedures. The significance of pilot plants is that they allow examination of formulas to determine suitability for batch scale-up and process modification. General considerations for pilot plants include having appropriate personnel, space, equipment, and procedures to support good manufacturing practices and product validation. The document also discusses advantages like quality control observation and material sourcing, as well as disadvantages such as potential reduced interaction between formulation and production teams.
Introduction Travetco
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1/5 Veterinary Medicine Company (TRAVETCO) was established in 1998, specializing in manufacturing and trading veterinary pharmaceutical products which meet the international standard.
Situated in Tra Noc 2 Industrial Zone of Can Tho City, the factory has modern equipment and machinery for production, inspection, and development of products with no-ceasing.
Thanks to the great efforts of the Board of Directors and well-trained workers, in March 2013, the factory of 1/5 Veterinary Medicine Company has been officially verified by the Veterinary Department and issued GMP-WHO certificates consisting of GMP ( Good Manufacturing Practices), GLP (Good Laboratory Practices),and GSP ( Good Storage Practices).
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systems – Requirements for regulatory
Purposes. ISO is an organization that develops Standards for use
worldwide.
ISO 13485 helps companies do their share in protecting
consumers and users of medical devices.
ISO 13485 Outlines criteria for a good Quality
Management System (QMS).
QMS criteria are good business practices ...
for example:
• Set Quality goals
• Ensure that regulations and other requirements are
understood and met
• Train employees
• Control your production processes
• Purchase from suppliers that can provide products that
meet your requirements
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2. NABL and ISO Principles
3. Need of NABL
4. Recognition of NABL in International Level
5. Scope of NABL
6. Advantages of NABL
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The document discusses the importance of written procedures, records, and quality control processes for ensuring Good Manufacturing Practices (GMP) compliance. It emphasizes that written procedures provide clear guidance, consistency, and help attain high quality standards. Maintaining thorough records is also essential as they document the manufacturing process and can be referenced in the event of complaints. The key aspects discussed are performance, pride in one's work, and having proof through documentation to demonstrate GMP compliance.
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ISO 17065 .pdf
Product certification or product qualification is the process of certifying that a certain
product has passed performance tests and quality assurance tests, and meets
qualification criteria stipulated in contracts, regulations, or specifications (sometimes
called "certification schemes" in the product certification industry).
Most product certification bodies (or product certifiers) are accredited to or aligned with
ISO/IEC 17065 Conformity assessment -- Requirements for bodies certifying products,
processes and services (previously ISO/IEC Guide 65:1996) an international standard
for ensuring competence in those organizations performing product, process and service
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standard. In India Product certification is being monitored by BUREAU OF INDIAN
STANDARDS.
Examples of some certification schemes include the Safety Equipment Institute for
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A Guide to Selling Compliant & Safe Children's Toys in The United States. Regional Product Safety Attaché (Asia-Pacific)
U.S. Embassy, BeijingVendor selection
Vendor selection and certification is important for pharmaceutical companies to ensure quality control and regulatory compliance. It involves categorizing vendors based on risk level and monitoring them accordingly. The key steps are:
1) Evaluating vendors based on criteria like quality, delivery, facilities, financials, and compliance history.
2) Classifying them into categories from 1 to 4 based on risk, with category 1 needing minimal oversight and category 4 requiring intense monitoring.
3) Qualifying vendors through assessing processes, specifications, changes, and customer inspections to ensure quality standards are met.
4) Conducting periodic audits and follow-up visits to ensure continued compliance. This helps build confidence and trust in the vendor-customer relationship.
validation ppt.pptx
The document discusses pharmaceutical validation requirements according to various regulatory bodies like USFDA, EU, WHO and cGMP. It explains the manufacturing process model involving three stages - process design, process qualification and continued process verification. It also describes the user requirement specification document and the different phases of qualification - design qualification, installation qualification, operational qualification and performance qualification. The qualifications are methods to demonstrate that equipment and processes will consistently produce products meeting quality standards.
Testing and Certification of Consumer Products (English)
This document provides an overview of the Consumer Product Safety Commission's third party testing program requirements. It discusses the requirements for initial certification testing, component part testing, material change testing, and periodic testing that manufacturers must follow to certify that children's products comply with safety standards. It also outlines the recordkeeping responsibilities and reasonable testing program best practices for non-children's products. The presentation emphasizes exercising due care in relying on third party test results and avoiding any undue influence on testing laboratories.
modulo-6-como-comprar-en-china.pdf
This document discusses various topics related to purchasing products from Alibaba and China, including:
- What Alibaba is and whether it is trustworthy
- Whether products from China are good
- How to contact potential suppliers on Alibaba
- Tips for safe purchasing on Alibaba such as using trade assurance
- Different shipping options like air vs sea freight
The document provides advice and answers frequently asked questions for importing products from China using Alibaba.
Cqe preparation | supplier management
Define, select, and apply various techniques including supplier qualification, certification, evaluation, ratings, performance
improvement, and so on.
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Vendor qualification
1) Vendor qualification is the process used by finished dosage form manufacturers to approve vendors for active pharmaceutical ingredients (APIs) that will be used in products. It involves selecting vendors based on criteria like quality, delivery, price, and auditing them.
2) Vendors are categorized as A, B, or C depending on which tests they perform on APIs. Category A vendors perform all tests, B vendors are well-known and certified, and C vendors undergo full testing by the manufacturer.
3) The vendor qualification process determines if a vendor is suitable and can consistently supply quality APIs. It aims to develop long-term supplier relationships and ensure regulatory expectations are met.
Si quality manual
This document describes a 4-level quality inspection system for Shareway Industries that meets the requirements of MIL-I-45208A. The primary purpose is to establish a quality control system to ensure acceptable product quality. Quality Assurance and management are responsible for implementing and maintaining the quality manual, which is reviewed annually and updated as needed. All revisions must be approved by the Quality Assurance Manager and company president.
China certificaitons introduction
China requires the China Compulsory Certification (CCC) for electronic equipment sold in China. CCC certification involves testing for safety and EMC standards, an initial factory inspection, and follow-up inspections. It must be renewed every 5 years and each certificate is only valid for a single manufacturer and factory. Products must be tested by an accredited Chinese lab and pass all China's national standards, which are typically harmonized with IEC standards. The CCC process can use previous CB test reports but all product details must match exactly between certificates to avoid delays. Factories are also inspected to ensure product quality and consistency with the certified sample.
CPSC Toy Fair Presentation - Third Party Testing Rules for Children's Product...
CPSC Toy Fair Presentation - Third Party Testing Rules for Children's Product...U.S. Consumer Product Safety Commission
The document summarizes new rules for third party testing of children's products that took effect in 2013. It outlines requirements for initial certification testing, component part testing, material change testing, and periodic testing for continued production. Manufacturers must have products tested by accredited laboratories, issue certificates of compliance, and maintain testing records. The rules aim to provide assurance that children's products meet safety standards for substances like lead and phthalates.Overview Section 1,2,3
This document summarizes sections 1, 2, and 3 of the AS9100C quality management system standard. Section 1 outlines the scope and applicability of the standard. Section 2 discusses exclusions from the standard's requirements. Section 3 defines key terms used in the standard, including special requirements, critical items, and key characteristics, and explains their interrelationships.
Api q1 6 a monogram-iso audit template- blank
This audit report form is used to audit organizations claiming conformity to API Spec Q1 9th Edition and ISO 9001:2015. It documents audit information such as the facility details, audit scope and criteria, license scope if applicable, quality management system requirements, procedures, and audit findings. Requirements specific to ISO 9001:2015 are highlighted. The auditor evaluates objective evidence to verify conformance and notes any nonconformities.
China medical device approval chart - EMERGO
1. The document outlines the regulatory process for medical devices in China, including classification of devices and the approval process for Class I, II, and III devices.
2. Class I devices have the simplest approval process, requiring only an administrative review with no submission fees. Class II and III devices require more extensive technical documentation, testing in China, and clinical evaluations.
3. The approval process can take 12-22 months for Class II and III devices and involves appointing a Chinese agent, submitting documentation and application materials in Chinese, testing, and a review by the China Food and Drug Administration before a registration certificate is issued.
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Selling Compliant & Safe Children's Toys in The United States (English)
Selling Compliant & Safe Children's Toys in The United States (English)
Testing and Certification of Consumer Products (English)
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5263 UPC CERTIFICATE
- 1. IAPMO Research and Testing, Inc. is a product certification body which tests and inspects samples taken from the supplier's stock or from the market or a combination of both to verify compliance to the requirements of applicable codes and standards. This activity is coupled with periodic surveillance of the supplier's factory and warehouses as well as the assessment of the supplier's Quality Assurance System. This listing is subject to the conditions set forth in the characteristics below and is not to be construed as any recommendation, assurance or guarantee by IAPMO Research and Testing, Inc. of the product acceptance by Authorities Having Jurisdiction. This listing period is based upon the last date of the month indicated on the Effective Date and Void After Date shown above. Any change in material, manufacturing process, marking or design without having first obtained the approval of the Product Certification Committee, or any evidence of non-compliance with applicable codes and standards or of inferior workmanship, may be deemed sufficient cause for revocation of this listing. Production of or reference to this form for advertising purposes may be made only by specific written permission of IAPMO Research and Testing, Inc. Any alteration of this certificate could be grounds for revocation of the listing. The most updated information on this Certificate of Listing is available online at pld.iapmo.org Effective Date: June 2015 Void After: June 2016 Product: Fill Valves (Anti-Siphon) File No. 5263 Issued To: XIAMEN VIB INDUSTRY & TRADE CO., LTD. Caitang Industrial Zone, Huli District Xiamen, FU JIAN 361009 China Identification: Manufacturer's name and trademark, model number, "1002" and critical level shall be permanently marked so as to be visible after installation. The product shall also bear the cUPC® certification mark. Characteristics: Anti-Siphon type flush tank fill valves (ballcocks) to be installed in accordance with the manufacturer's instructions and the requirements of the latest edition of the Uniform Plumbing Code®. Products listed on this certificate have been tested by an IAPMO R&T recognized laboratory. This recognition has been granted based upon the laboratory's compliance to the applicable requirements of ISO/IEC 17025. Products are in compliance with the following code(s): Uniform Plumbing Code (UPC®) National Plumbing Code of Canada International Plumbing Code (IPC®)
- 2. Page 2 Void After: June 2016 Product: Fill Valves (Anti-Siphon) File No. 5263 Issued To: XIAMEN VIB INDUSTRY & TRADE CO., LTD. Products are in compliance with the following standard(s): ASSE 1002-2008 and CSA B125.3-2012
- 3. MODELS: J103, J13010, J13011 Page 3 Void After: June 2016 Product: Fill Valves (Anti-Siphon) File No. 5263 Issued To: Xiamen Vib Industry & Trade Co., Ltd.