Checking Agencies

Motor Fleet Safety and Security Management Credit Checking Agencies... 

Because not everyone is honest, it is important to verify the information provided on applications, and it is a good idea to use a credit checking agency With credit checks, you can see where applicants have lived in the past and sometimes what kind of lifestyle they may have led. ... 

Recommendations and regulations are also periodically updated as more information becomes available. For the most current information, check with the federal agency or organization that provides it. Some regulations and recommendations for methyl parathion include the following ... 

The audit also emphasizes the self-regulated nature of the industry and the ideal relationship between the agency and the industry. In theory and effective practice, a biomedical company utilizes its quality assurance (QA) unit (in this case, supplemented by credible Part 11 auditors) to maintain control of safety, effectiveness, and quality. The FDA can then review the quality system (QS) and spot-check the other systems such as laboratory or production for most efficient regulatory oversight. In effect, the QA regulates the company and the FDA regulates the QA. 

Is the application or system used to automate a manual QC check of data subject to review by a regulatory agency ... 

This safety check is in the first approach a check the responsible manufacturer or importer has to do in his own responsibility. In a second approach, it is to some extent also a check which is done by the competent authorities, especially the European Chemicals Agency (ECHA) and the national authorities. 

The Current Position. This could soon change and readers are advised to check these points on the food standards agency website (www.foodstandards.gov.uk). 

When all equipment is removed from the decontamination site, the containment pits will be sprayed with decontamination solution, rinsed, and checked for contamination. All bag items meant for disposal will be picked up by another agency. Once the site has been... 

In pharmaceuticals, NIR is used for, of course, moisture, polymorphic (drug) forms, percent crystallinity, isomer purity, tablet/capsule assay, coating levels, evaluation of dissolution times, and numerous process tests. It is a rapid means for the Food and Drug Administration to check for counterfeit drugs, and for the Drug Enforcement Agency to ascertain what type of materials are impounded in drug raids. ... 

A proficiency testing scheme is defined as a system for objectively checking laboratory results by an external agency. It includes comparison of a... 

Reference and research methods. These are generally more sophisticated procedures that are used by central quality control laboratories or by government agencies with qualified personnel. These methods are often used to verify results obtained by the rapid methods described below or to calibrate the instruments. They may also be used to verify additives declared on the label of a food product or to check for the use of non-permitted additives. This aspect is of increasing importance since legislation may vaiy between different countries, and food products are frequently subject to inter-market exports . The most important characteristics of these analytical procedures are ... 

For the most reliable results, chamber environment should be monitored continuously with instruments and techniques equivalent to those used in ambient-air monitoring networks (see Chapter 6). Calibration of instruments should follow recommendations by appropriate agencies and be checked by cross comparisons with those in other analytic laboratories. 

The identification number of the transporter and the receiving facihty and their valid hazardous waste hcenses must be double checked with the State s regulatory agency. 

Responsibility for regulatory review has been passed to an Incorporated Administrative Agency, the Pharmaceutical and Medical Devices Agency (PMDA). PMDA also intensively checks applications for GCP compliance and reliability compliance. Another important role of PMDA includes an advice to sponsors on clinical trials and on which result can be submitted at the time of a new drug application. 

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