Suppliers health

Supplier sensing. Active sensing of the health of the supplier relationship and setting up programs that improve supplier health. This includes financial terms, order policies, transportation and freight requirements, and adherence to CSR programs. 

The service value netwoik in an e-pharmacy setting is hereby defined as acollaborative network of supply chain partners (such as pharmacists, drug companies, distributors, beauty care suppliers, health and natural product suppliers, medical practitioners) sales channels (Web site e-sales, direct over-the-counter sales, and referrals) and operational and network administration personnel, working with and serving the needs of its customers and its online e-customers. 

In line with its stated intent, the standard is a process standard and specifies design and risk management activities required of medical device suppliers, health organisations and other IT vendors when medical devices are connected to a generic IT network. In order to ensure harmonisation of standards, the risk management processes described in IEC80001 mirror those expected in the Medical Device Directive. 

Go to the Web and develop a list of suppliers along with unit costs for some of the various types of flocculants described in this chapter. Also obtain the MSDS (Material Safety Data Sheets) for these chemicals. Once you have collected the information, develop a relative ranking of unit cost and health risk associated with each. For question 2 you will need information of recommended doses. 

The first step is to identify the substances present at the workplace. As a starting point, knowledge of the process is needed in order to formulate a list of all chemical agents used in the establishment. The list should include not only primary products but also intermediate and final products, as well as reaction products and by-products. For the chemical agents in the list, it is necessary to know their chemical properties, especially hazardous ones their OEL values, including biological limit values and, where these are not available, other technical criteria that can be used to evaluate the risk. It is also helpful to include any information on the safety and health risks of those substances provided by the supplier or other readily available sources. This information on dangerous substances and preparations, in the form of safety data sheets, is intended primarily for industrial users, to enable them to take the measures necessary to ensure the safety and health of workers. 

The business quality dimension. This is the extent to which the business services the needs of society. Customers are not only interested in the quality of particular products and services but judge suppliers by the general level of quality products they provide and continuity of supply, their care of the environment, and their adherence to health, safety, and legal regulations. 

Regulatory requirements may apply to health, safety, environmental emissions, and electromagnetic compatibility and these often require accompanying certification of compliance. In cases where customers require suppliers to be certified to ISO/TS 16949 it imposes a regulatory requirement on the design process. 

In the event of accident or gross misuse of products, various health hazards could arise. The data provided by the supplier should outline these potential hazards and the simple precautions that can be taken to minimize them. Guidance should be included on the remedial action that should be taken to deal with medical conditions that might arise. Advice should be obtained from the supplier before petroleum products are used in any way other than as directed. 

Section 6 of the Act has been amended by the Consumer Protection Act 1987 and now imposes specific duties on manufacturers, importers, designers and suppliers to ensure that articles and substance supplied for use at work are safe and without risk to health. 

To assist manufactures and suppliers attain the required level of health and safety, the Health and Safety Commission have commenced approving standards laid down by such bodies as the British Standards Institution. 

Numerous leaflets can be obtained from the local offices of the Health and Safety Executive or HSE Information Points. Remember, if you have any doubts about the health and safety risks involved with respect to any substance you may consider using, or any work you are planning to undertake, seek advice. This information may be obtained from your company safety officer, consultants, manufac-turer/supplier or equipment/materiaPsubstance, HSE or local Environmental Health Officer. Use their expertise and knowledge. Do not be a statistic. 

In establishing potential hazards in carrying out specific tasks, other sources may have to be consulted (e.g. manufacturer, supplier, HSE, environmental health officer, consultants, etc.) and protective clothing and equipment must be considered. 

Search MSDS on CCINFOWeb. All databases on CCINFOWeb may be searched for free. The MSDSs are contributed by North American sources, many that are multi-national companies marketing chemical products worldwide. This database meets a growing international requirement for health and safety information on specific chemical products. It helps thousands of users worldwide manage their responsibilities under workplace, environmental and other right-to-know legislation. The MSDS database can be searched quickly and easily for product names and other product identifications, manufacturer or supplier names, dates of MSDSs, or any term used in the text of the MSDS itself. 

We can expect drastic changes in the food packaging industry. Some will arise from new consumer needs, new or expanded food supplies and products, and new food preservation systems such as aseptic packaging. Others will result from societally based constraints such as safety in health and hazardous use (as in the child safety closure legislation) and consumer protection against fraud, misinformation, or wrongful use where the burden for awareness is no longer on the buyer but on the supplier. Other such constraints will arise from environmental concerns or material scarcities. 

Material Safety Data Sheets (OSHA Form 20, see Figure 1) are available from suppliers for every chemical sold. These give valuable information of a specific nature and should be kept on file. A phone call to the nearest office of the Occupational Safety and Health Administration (OSHA) of the U.S. Department of Labor will bring forth more information on safety, both oral and written. 

In contrast to specifying to suppliers what chemicals or materials are restricted, it is useful to specify exactly what chemicals and materials are desired. Once a material or chemical is well characterized, and it is considered benign with respect to human and environmental health, it can be added to a preferred or positive list (i.e., P-list). For example, a textile manufacturer may source certified organic cotton, or polyester made with antimony-free catalysts, to develop a product line based on these fibres. Or a cleaning product formulator may seek bio-based solvents or rapidly biodegradable surfactants consistent with their product development objectives. 

A good example of the many successftil DfE Partnerships is the Furniture Flame Retard-ancy Partnerhip. Pentabromodiphenylether (PentaBDE) was the primary flame retardant used in low density, flexible polyurethane furniture foam. Due to concerns over its use and the fact that the chemical was found widespread in the environment and in human tissue and breast milk, PentaBDE was voluntarily phased out of production by US manufacturers in January 2004. The industry needed alternatives in order to meet furniture flame retardancy requirements, but did not have the human and environmental health and safety information needed in order to compare the alternatives. DfE worked with the furniture manufacturers, foam manufacturers, and flame-retardant chemical suppliers along with governmental and environmental groups to evaluate possible alternatives. 

All the data on health and fire/explosion hazards for compounds and (if possible) mixtures to be dealt with in a process should be collected in the form of an MSDS (Material Safety Data Sheet). It is common practice for users to require that suppliers attach an MSDS to all batches of materials delivered. 

In the design of equipment for the manufacture of sterile ophthalmic (and nonophthalmic) pharmaceuticals, manufacturers and equipment suppliers are turning to the advanced technology in use in the dairy and aerospace industries, where such concepts as CIP (clean-in-place), COP (clean-out-of-place), automatic heliarc welding, and electropolishing have been in use for several years. As a guide here, the reader is referred to the so-called 3A Standards of the dairy industry issued by the U.S. Public Health Service [267],... 

API is not undertaking to meet the duties of employers, manufacturers, or suppliers to warn and properly train and equip their employees, and others exposed, concerning health and safety risks and precautions, nor undertaking their obligations under local, state, or federal laws. 

Information concerning safety and health risks and proper precautions with respect to particular materials and conditions should be obtained from the employer, the manufacturer or supplier of that material, or the material safety data sheet. 

Packaging companies, input suppliers strict standards on health and safety and the environment need to be supported by high standard chemicals and equipment, properly packaged and available in quantities that encourage safe and proper application ... 

IDLH Immediately Dangerous to Life or Health levels indicate that exposure to the listed concentrations of airborne contaminants is likely to cause death, immediate or delayed permanent adverse health effects, or prevent escape from the contaminated environment in a short period of time, typically 30 min or less. These values constitute a hazardous materials emergency in the workplace and require the use of a supplier air respirator (e.g., SCBA). 

Priority substances were selected, which are considered to be of particular concern to human health and/or the environment. The suppliers of these priority substances had to provide any missing studies to complete a EU notification Base Set (Table 1). A rapporteur Competent Authority evaluates the full review dossier on behalf of the EU. The final output is a risk assessment (see Section 14), with final recommendations on how to deal with the substance i.e., it may be of no concern, require risk reduction or restriction, or further data may be needed before a decision is made. 

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