Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Production records

Are production log sheets and production records kept for a minimum of one year If not, how long ... [Pg.160]

Maintenance and production records, along with the used lean and rich glycol analyses, can be very helpful to the troubleshooter. A history of filter element, carbon, tower packing, and firetube changeouts can sometimes be very revealing. The frequency of pump repairs and chemical cleaning jobs is also beneficial. With this type of knowledge, the troubleshooter can quickly eliminate and prevent costly problems. [Pg.323]

In 1931 Ing pointed out that formula (II) and (III) do not contain methyl or potential methyl groups in j ositions 6 and 8 which they occupy in cytisoline. Further, a partially reduced quinoline ought to oxidise easily to a benzenecarboxylic acid and so far the only simple oxidation, products recorded from cytisine were ammonia, oxalic acid and isovaleric acid. Distillation of cytisine with zinc dust or soda-lime yields pyrrole and pyridine, but no quinoline. On these grounds Ing suggested that cytisine should be formulated without a quinoline nucleus, and that the reactions which indicate the presence of an aromatic nucleus in the alkaloid can be accounted for by an a-pyridone ring. This a-pyridone nucleus can... [Pg.143]

Is lost, damaged, or unsuitable customer supplied product recorded and reported to the customer ... [Pg.82]

The design verification plan should be constructed so that every design requirement is verified and the simplest way of confirming this is to produce a verification matrix of requirement against verification methods. You need to cover all the requirements, those that can be verified by test, by inspection, by analysis, by simulation or demonstration, or simply by validation of product records. For those requirements to be verified by test, a test specification will need to be produced. The test specification should specify which characteristics are to be measured in terms of parameters and limits and the conditions under which they are to be measured. [Pg.260]

Make provision on all product records for the product identification to be recorded. [Pg.343]

Quality control - responsibility, review test results and production records, retain samples... [Pg.213]

Batch Production Records (Batch Production and Control Records)... [Pg.216]

Sec. 820.182 Device history record - Maintain the production records for each batch of devices Sec. 820.186 Quality system record - Compile or refer to location of general procedures relating... [Pg.234]

NOj from sporadic solar proton events maximum production recorded in August, 1972 1 X 10 °moles produced. [Pg.152]

Master production and control records. 211.188 Batch production and control records. 211.192 Production record review. [Pg.13]

The weight or measure is correct as stated in the batch production records ... [Pg.36]

Stabilisers are usually determined by a time-consuming extraction from the polymer, followed by an IR or UV spectrophotometric measurement on the extract. Most stabilisers are complex aromatic compounds which exhibit intense UV absorption and therefore should show luminescence in many cases. The fluorescence emission spectra of Irgafos 168 and its phosphate degradation product, recorded in hexane at an excitation wavelength of 270 nm, are not spectrally distinct. However, the fluorescence quantum yield of the phosphate greatly exceeds that of the phosphite and this difference may enable quantitation of the phosphate concentration [150]. The application of emission spectroscopy to additive analysis was illustrated for Nonox Cl (/V./V -di-/i-naphthyl-p-phcnylene-diamine) [149] with fluorescence ex/em peaks at 392/490 nm and phosphorescence ex/em at 382/516 nm. Parker and Barnes [151] have reported the use of fluorescence for the determination of V-phenyl-l-naphthylamine and N-phenyl-2-naphthylamine in extracted vulcanised rubber. While pine tar and other additives in the rubber seriously interfered with the absorption spectrophotometric method this was not the case with the fluoromet-ric method. [Pg.322]

The eggs were collected daily and were kept under refrigeration until they were analyzed for their DDT content. Feed consumption and production records were kept for each hen. The data on weight gains, food consumption, and egg production will be published at the end of a 3-year feeding period. [Pg.233]

Analyzing Data Use the masses in the table to calculate the mass of the magnesium ribbon and the mass of the magnesium product. Record these masses in the table. [Pg.31]

Master Production Instructions Batch Production Records Laboratory Control Records Batch Production Record Review Materials Management General Controls Receipt and Quarantine... [Pg.285]

Sterile Products Personnel, Buildings, Air, Environmental Controls, Equipment, WFI, Containers and Closures, Sterilization, Laboratory Controls, Production Records... [Pg.329]

Your teacher will give you a table that lists four equilibrium systems and the changes you will make to each system. In the appropriate column, record your predictions for each test. If you predict that the change will cause the system to re-attain equilibrium by shifting toward the reactants, record left. If you predict that the system will re-establish equilibrium by shifting toward the products, record right. ... [Pg.358]

Maintenance of adequate and accurate records forms an essential part of GMP. For any given batch of product, records relating to every aspect of manufacture of that batch will be retained. These records will include ... [Pg.111]

ABC Pharmaceutical Industries information. Weighing of a lot follows detailed step-by-step instructions as outlined in the batch production record. Weighing of all ingredient materials is accomplished in a dedicated room within the class 100 air quality. The preweighed ingredients are transported to the mixing/compounding area. [Pg.490]

The equipment sterilization charts are included in the batch production record. The equipment sterilization charts for stability batch are produced in support of this submission. These sterilization charts shall be reviewed by Quality Assurance for adherence to the sterilization cycles specified in the batch records. [Pg.513]


See other pages where Production records is mentioned: [Pg.36]    [Pg.126]    [Pg.51]    [Pg.215]    [Pg.216]    [Pg.26]    [Pg.16]    [Pg.37]    [Pg.42]    [Pg.42]    [Pg.44]    [Pg.44]    [Pg.68]    [Pg.219]    [Pg.373]    [Pg.304]    [Pg.306]    [Pg.348]    [Pg.315]    [Pg.328]    [Pg.220]    [Pg.413]    [Pg.37]    [Pg.126]    [Pg.82]    [Pg.124]    [Pg.5]    [Pg.11]    [Pg.12]   
See also in sourсe #XX -- [ Pg.144 ]




SEARCH



Batch production record, specification

Batch production records

Flower Production Records

Master production and control records

Product Sample Records

Production of Photographic Records (Photofacsimile)

Recording the actual condition of nonconforming product

© 2024 chempedia.info