Certification locations

Certified testing and approval for control-valve devices used in hazardous locations is normally procured by the manufacturer of the device. The manufacturer often goes to a third party laboratory for testing and certification. Applicable approval standards are available from CSA, CENELEC, EM, SAA, and UL. 

Certification of motors used in hazardous locations 11/266 Further reading 11 /272... 

While some video display screens such as liquid crystal, gas plasma or vacuum fluorescent displays do not present the same charged screen hazards as CRTs, this does not imply that they are safe for use in hazardous locations. This requires special design and certification for use with a given flammable atmosphere. Non-certified equipment used in locations classified as hazardous under Article 500 of NFPA 70 National Electrical Code require a purged or pressurized enclosure to control ignition hazards as described in NFPA 496 Standard for Purged and Pressurized Enclosures for Electrical Equipment. The screen in this case is located behind a window in the enclosure. 

Most of the information required In Part I and all of the Information required In Part II of Form R can be filled In and photocopied and attached to each chemical-specific report. Part I must have an original signature on the certification statement and the trade secret designation must be entered as appropriate. You have the option to complete Part II for only the off-site locations that apply to the Individual chemical cited In the report g you can list all off-site locations that apply to all chemicals being reported and Include a photostatic copy of this Part II with each individual report. Part III must be completed separately for each chemical. Part IV provides additional space, if needed, to complete the information required by the preceding sections of the form. Include Part IV In your report, even it it Is blank. 

Enter the name and telephone number (including area code) of a technical representative whom EPA or State officials may contact for clarification of the information reported on Form R. This contact person does not have to be the same person who prepares the report or signs the certification statement and does not necessarily need to be someone at the location of the reporting facility however, this person must be familiar with the details of the report so that he or she can answer questions about the information provided. 

Certification to the standard will only be awarded to a site that has the capability to meet all the applicable requirements of ISO/TS 16949 for the products and services concerned. If some operations are carried at remote locations (e.g. design centers and corporate headquarters), such locations cannot receive separate certification and must be included within the certification awarded to the parent site possessing production capability. 

Remote locations shall be audited as they support a site but cannot obtain independent ISO/TS 16949 certification. A division that does not have the capability to meet all requirements cannot seek ISO/TS 16949 certification e.g. Personnel, Purchasing divisions cannot be registered separately as they could be under ISO 10011. 

The entire quality system shall be assessed at a minimum of once every three years. The audit plan for a supplier has to cover all requirements, all sites, all locations, all operations, all functions, all customers, all processes, all procedures at least once in a three-year cycle, unless it is an upgrade certification (see clause 4.6). Hence the sample of operations taken on each audit has to cover at least Veth of the whole. 

If testing involves a new product that is not yet in commercial trade, the manufacturer should ship products from the same batch of the same formulation to each test location. The most recent product quality analysis and an appropriate Material Safety Data Sheet (MSDS) must accompany the product shipment. The shipping documents and the certificate of analysis for each shipment must be archived in the raw data for the report. If the residue testing is being done to register a new use for a commercial product, the Study Director must make sure that the product available in each location is the same formulation and that each different batch encountered has its own certificate of analysis to be archived along with a copy of the label and product quality analysis of the material used for the test. Material shipped in noncommercial containers must... 

In spite of the rigorous design requirements and the need for certification, instrinsically safe electrical circuits offer many advantages which the other hazardous location electrical techniques do not. 

Located additional documents and manufacturer s certificates and placed them In the proper locatlon(s), as specified In this protocol ... 

The only study located regarding developmental effects reported no adverse effects on human fetal development following transplacental exposure to heptachlor based on birth certificate information and hospital discharge data (Le Marchand et al. 1986). The study was conducted on women of child-bearing age from Oahu, Hawaii, who ingested milk containing heptachlor for 27-29 months. 

Where is it possible or desirable to locate the near-infrared analyzer modnle What hazardous area certification requirements apply to both analyzer and sampling system ... 

Each item listed in this section of your resume should include the name of the educational institution you attended, the date of completion, the degree or certificate earned, and the city and state where the institution is located. 

Both samples are in the form of pellets containing antioxidants as specified on the certificates. They have also been examined for sample homogeneity by dilute-solution viscosity. In the case of the linear material, SRM 1475, although the lot is uniform with respect to location, a measurable pellet-to-pellet variation exists. To make certain that a uniform sample is obtained, at least one gram of pellets should be blended to reduce the expectation of error from pellet variability to less than 0.5%. The branched material on the other hand is quite uniform and does not show pellet-to-pellet variation. Both materials have low ash and volatile content. 

Location of personal papers Provide all the help you can here. Give the exact location of your personal documents, including birth certificate, marriage certificate, diplomas, military papers, and so on. It s a good idea to gather these in a single location. 

Investments For some people, this can be most important. List all stocks, bonds, certificates of deposit, IRA or Keogh accounts, and other investments. Include issuer name and cost to you. Also indicate where items are located. Identify your stockbroker and other agents. If you have any gold coins or silver bars that constitute an investment, provide location and details. 

A certification must be sent to the FDA by the company, which informs the FDA that electronic signatures will be used. This certification can be a global statement of intent, meaning that a single company certification can cover all systems, all applications, all of the electronic signatures, for all employees in a company, for all the firm s locations anywhere in the world. The Regulatory Affairs Unit of the company will usually send this certification to the FDA. 

If you are going to sign documents, have ready a certificate file contammg a pubkc key. the wizard w prompt vou far location of this certificate on yoi file system. 9... 

This page is used to specify the location of the certificate file. Each submission must be accompanied by a certificate. The digital certificate must be an X.509 version 3 certificate. 

---