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Quality operational

Because some hydrocracking occurs, Powerforming also produces saturated C to Q light hydrocarbons. The methane and ethane formed normally are consumed as refinery fuel. Propane and butane products are frequently marketed as LPG. The relative quantities of each of these products vary considerably with feed quality, operating conditions and octane severity. [Pg.48]

Limit maximum or minimum setpoint inputs to stay in safe and quality operating regions. [Pg.109]

The standard requires tends in quality, operational performance (productivity, costs of poor quality, efficiency, effectiveness) and current quality levels for key product and service features to be documented. [Pg.144]

When using ZSM-5, there is almost an even trade-off between FCC gasoline volume and LPG yield. For a one-number increase in the research octane of FCC gasoline, there is a 1 vol% to 1.5 vol% decrease in the gasoline and almost a corresponding increase in the LPG. This again depends on feed quality, operating parameters, and base octane. [Pg.121]

Hydrocomp Inc. Hydrocomp Water Quality Operations Manual. [Pg.146]

Some of these government agencies and private companies, because of the nature of their business, will utilize the services of an analytical chemistry laboratory as part of their overall need to assure the required quality operation. For example, municipal governments will employ the use of an analytical chemistry laboratory to test their water supply on a regular basis to make sure it is free of toxic chemicals. The pharmaceutical company will house an analytical chemistry laboratory within its facility to routinely test the products it produces and the raw materials that go into these products to make certain that they meet the required specifications. A fertilizer plant will utilize an analytical chemistry laboratory to confirm that the composition of its product meets the specifications indicated on the individual bags of fertilizer. Companies that produce a food product, such as snack chips, cheese, cereal, or meat products, will have an analytical chemistry laboratory as part of their operation because they want to have the assurance that the... [Pg.9]

The management reviews are conducted with a planned agenda to provide direction for the company s quality operations. Input from outside and inside sources are welcome to ensure continuous improvement. The audit findings and areas of quality concern are discussed. It is ensured that corrective and preventive measures are taken on time. The review input includes statistical evaluation of process performance and product conformity. [Pg.270]

The APR committee will consist of the following key personnel site general manager, executive director of quality operations, and director of manufacturing. [Pg.527]

Quality assurance must also have a formal system in place to thoroughly investigate product complaints that are referred to quality operations for an assessment. Criteria and guidelines should be developed that provide a standardized framework for comprehensive complaint investigations. Additionally, periodic trending of all quality investigations should be... [Pg.536]

This chapter discusses management s role in creating an effective overall quality operation and provides some insights into and techniques to address specific regulatory threats. [Pg.584]

As described in Section 1.1, the goal of the simulation study is to quantify the relationships between the simulation outputs and the inputs or factors. For this case study, the outputs are the steady-state mean costs of the whole supply chain (discussed in Section 3.2) and the inputs are factors such as lead-time, quality, operation time of an individual process, and number of resources. Our ultimate goal (as reported by Kleijnen et al., 2003) is to find robust solutions for the supply chain problem. Thus we distinguish between two types of factors ... [Pg.292]

There are no additional or reduced regulatory requirements for closing sites. Computer systems should be maintained in a validated state of compliance up until the very last day of their operational life. GxP records must be archived and stored for the required retention periods. Archived records should be readily retrievable to support critical quality operations like recall, customer complaints, and batch investigation. Computer systems should then be decommissioned, as discussed later in this chapter. Some computer systems may be disassembled and sent for installation at other sites as part of a program of drug product transfers. [Pg.318]

Critical quality operations like recall, customer complaints, and batch investigation... [Pg.338]

Roger Dean is a Fellow of Royal Institute of Chemistry, an Associate of Institute of Managers, and a Graduate of Royal Institute of Chemistry by examination. Mr. Dean has spent 14 years in Quality Control/Analytical Chemistry and 2 years in Production Chemistry at Beecham Pharmaceuticals, and 11 years in Quality Operations/Analytical Chemistry and 9 years in IT support and projects at Pfizer Limited (Pharmaceuticals). Mr. Dean has also been involved in project managing the implementation of an EDMS system with significant involvement in its design and validation and also in several other vahdation projects. [Pg.965]

Addition of chemicals is not required Effluent quality is independent of feed quality Operation at ambient temperature Forms an absolute barrier to pathogens Space efficient... [Pg.247]

The writing and implementation of SOPs form the framework of a quality operation by defining expectations and providing a consistent approach... [Pg.131]

Oxygen-based combustion delivers several control benefits that allow the operator to improve glass quality. Operators of regenerative furnaces are limited in tailoring the furnace profile by the flow patterns within the checkers. As noted previously, these flow patterns can change as the furnace ages. Oxy/fuel burners allow the... [Pg.233]

To establish quality assurance, control of dosage forms, starting from clinical trial to production for market introduction, must be imposed on in-process operations and product testing for compliance with the specifications and guidelines of quality operation to ensure product attributes. Occasionally, specifications may be revised because of new evidence discovered in the continuous preformulation study. [Pg.179]

As demonstrated by common elements of the guidelines and regulations, quality, process safety, and environmental responsibility are interrelated. If a facility is free of accidents, quality is easier to achieve or maintain. A safe, quality-conscious facility will likely be an environmentally responsible facility. The elements of process safety, including efective, controlled procedures, combine to achieve the overall goal of a safe, environmentally responsible, quality operation. [Pg.11]

The purpose of your procedure management system is to define how you will consistently develop, review, approve, implement, maintain, and control your procedures. Describing your procedure managonent system in a written, administrative procedure is a recognized and effective way to clearly establish those instmctions. The procedure manag ent system is based on your available resources (human, technical, and financial) and the hazard potential of the processes involved. Remember, your objective is to achieve a safe, environmentally responsible, quality operation. [Pg.22]

Immunoassays developed along the recommendations provided above should perform consistently and generate reliable data over time. However, occasional failures happen variations in laboratory environmental conditions, reagent quality, operator skill, and instalment performance, for example, make systematic troubleshooting skills invaluable in discerning the cause for assay failures. [Pg.70]

It is recommended that any intending user of sampling plans should examine these documents closely, since they have the major advantage of being internationally accepted and practised. Procedures are very clearly explained and a knowledge of statistics is not essential to their implementation, although a clearer understanding of their derivation and scope will aid the total quality operation. [Pg.89]

Proximity to prior scratches Optical/microscope quality Operator skill... [Pg.348]


See other pages where Quality operational is mentioned: [Pg.1877]    [Pg.2221]    [Pg.78]    [Pg.139]    [Pg.537]    [Pg.474]    [Pg.168]    [Pg.779]    [Pg.883]    [Pg.169]    [Pg.41]    [Pg.536]    [Pg.71]    [Pg.5]    [Pg.1636]    [Pg.1525]    [Pg.2319]    [Pg.2464]    [Pg.14]    [Pg.26]    [Pg.709]    [Pg.368]    [Pg.368]    [Pg.2302]    [Pg.2445]    [Pg.62]    [Pg.1881]    [Pg.2225]   
See also in sourсe #XX -- [ Pg.212 ]

See also in sourсe #XX -- [ Pg.119 ]




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