Controlling department

As stated above the Surveyor s role will include an assessment of the yard s quality control department including the suppliers of any contracted NDE services. The Surveyor will look for the employment of qualified personnel, the availability of adequate inspection procedures and the presentation of definitive NDE reports. 

Carbonated Beverage Quality Control Manual, Vol. II, Beverage QuaHty Control Department, Coca-Cola USA, Adanta, Ga., 1989. 

Quality control is also the term used as the name of a department. In most cases Quality Control Departments perform inspection and test activities and the name derives from the authority that such departments have been given. They sort good products from bad products and authorize the release of the good products. It is also common to find that Quality Control Departments perform supplier control activities, which are called Supplier Quality Assurance or Vendor Control. In this respect they are authorized to release products from suppliers into the organization either from the supplier s premises or on receipt in the organization. 

Description of the Quality Control system and of the activities of the Quality Control Department Procedures for the release of finished products. 

In a production environment, the quality control department does not ordinarily concern itself with single applications of analytical methods, that... 

The manufacturing and quality control departments face higher costs because they have to eliminate process and measurement variability, even if they are already operating at the technological limit. They will have to add people to their staffs to mn all of the investigations and handle the additional paperwork (because malicious intent is suspected, peers and supervisors have to sign off at every step to confirm that each SOP was strictly adhered to whether the SOPs made sense, scientifically speaking, or were installed to satisfy formalistic requirements is of no interest here). 

If the product is to be used for pharmaceuticals the GMP rules must be obeyed during plant operation. All chemicals to be tested in clinical studies with humans must be prepared according to GMP. This leads to very detailed documentation since if you haven t documented it, you haven t done it . All procedures for manufacturing and changes in procedures are subject to approval by quality control departments. This decreases the flexibility in process development. Products that are contaminated too much must be reprocessed according to the GMP guidelines. All equipment to be used in the pilot plant must be validated before use. 

Chemical Accident Contamination Control. Department of the Army Field Manual FM 3-21,1978. 

MA Div. Air Qual. Con. 1998. Allowable ambient limit. Massachusetts Division of Air Quality Control, Department of Environmental Protection. MA General Law, C 142, Sec A-E. 

TN Water Pol. Con. 1998. Criteria for water uses. Tennessee Water Pollution Control, Department of Environment and Conservation. Ch. 1200-4-3.03. 

The pharmacopeias have worked with the ICH process to facilitate the international environment of pharmaceutical research and product registration. On the other hand, the additional situation for compendia is that the standards which they have published now apply to all of the already marketed products. In that case a company has testing history and product history in their quality control departments. These are the most conservative elements within the pharmaceutical industry as is necessary to their task. Quality control departments are reluctant to change methods when they feel that their products are properly represented by the current of tests. Therefore, a tension is ereated between trying to develop harmonized standards, which facilitate one area of activity in the world of pharmaeeutieals, and not disturbing a satisfactory marketplace. A vast amount of progress has been made in the harmonization of phar-maeopeial methods. 

Results of all sampling are recorded and achieved in the Quality Control Department. 

QUALITY CONTROL DEPARTMENT Microbological Laboratories VISUAL INSPECTION REPORT... 

QUALITY CONTROL DEPARTMENT WATER ANALYTICAL REPORT... 

Training for the staff of the companies on the concept of ChL. It is recommended to include staff from the environment and quality control department, the purchasing department, the legal department (if any), technical and operational staff, and others. 

C.02.013 (Quality Control Department), C.02.015 (Quality Control Department), and C.02.024 (Records). Correspondences to regulation 211.22 are covered in... 

Subchapters 2.6 and 2.7 deal with the responsibilities of the head of the quality control unit (quality control department) and 6.2 with the responsibihties of the quality control unit as a whole. Requirements for resources are covered in Subchapter 6.1. Correspondences to regulation 211.25 are covered in Subchapters... 

Correspondences in Canadian GMP Code In the Canadian GMP code [12] issues related to production and process controls are mainly covered in the interpretation of regulation C.02.011 (Manufacturing Control) and partly in the interpretations of regulations C.02.005 (Equipment), C.02.014 (Quality Control Department), and... 

In many pharmaceutical companies, quality control departments already use NIRS to identify formulations. Figure 23 illustrates a PLS calibration for the active content determination in a low-dose tablet. Once identity testing is passed, it is straightforward to consider as a next step the determination of active content in intact tablets. Thus, qualitative and quantitative analysis can be performed by acquiring a single NIR spectrum per sample. Two analytical techniques are replaced by one—nondestructive—NIR measurement. For this purpose near-infrared spectroscopy is a fast and powerful alternative to traditional analysis, which only remains necessary as reference analytics. 

The physical properties and specifications for the manufactured formulations should match those established earlier by the product formulator, the pilot plant staff, and the quality control department. Therefore, the product manufactured on a large scale should possess the appropriate quality properties. 

Administration (Management) QUA = Quality Assurance = Production QCD = Quality Control Department... 

Winery A is very large and has a well staffed and departmented laboratory. It has a separate quality control department, but it is located in the main laboratory and performs its whole function within the confines of the bottling room, warehouse, and laboratory. In this example, the laboratory quality control department has Phase II as its total area of responsibility. A system of mechanical and routine inspections against a check list works perfectly. 

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