scholarly journals Correlation between “Pointing and Calling” method in manufacturing and degree of fatigue at a pharmaceutical manufacturing plant

2020 ◽  
Vol 2020 (30) ◽  
pp. 438-443
Author(s):  
Takeichiro Sudo ◽  
Kosuke Kiyohara
1984 ◽  
Vol 26 (10) ◽  
pp. 734-736 ◽  
Author(s):  
James R. Nethercott ◽  
Murray J. Lawrence ◽  
Anne-Marie Roy ◽  
Brian L. Gibson

2020 ◽  
Vol 53 (2) ◽  
pp. 11601-11606
Author(s):  
David Pérez Piñeiro ◽  
Anastasia Nikolakopoulou ◽  
Johannes Jäschke ◽  
Richard D. Braatz

1998 ◽  
Vol 38 (8-9) ◽  
pp. 1-8 ◽  
Author(s):  
Youngchul Kim ◽  
Wesley O. Pipes ◽  
Paul-Gene Chung

A full scale experiment with an activated sludge process in a pharmaceutical manufacturing plant showed that the operation of two settling tanks in series, with the first tank full of sludge, resulted in selection of sludge particles which had a lower than average filament content for retention in the process. Series operation of the two clarifiers was very successful in controlling sludge bulking. The functioning of the settling tanks as selectors of sludge particles which settle and thicken well has not been considered to any great extent. Two laboratory-scale activated sludge plants fed with an artificial wastewater were operated to explore this selection function further. The SVI values were measured and assessed. At the start of operation, the SVI was about 60–80 ml/g in both of the parallel and the series plants. After eight days of the operation, the SVI started to increase rapidly in the parallel plant, and in twenty days of operation, the averaged values of SVI were 163 ml/g and 116 ml/g for the parallel and the series plants, respectively. On day 38, MLSS from two aeration tanks were interchanged. In a few days after that interchange, the SVI values in the parallel, which was originally in the series mode, rapidly increased from 130 ml/g to more than 350 ml/g(SV30 = 930 ml/g). This experiment clearly supports the hypothesis of a microorganism selection function of the settling tank and also corresponds to the results obtained from the field study.


Author(s):  
Amit B Patil ◽  
Bharath Kumar B ◽  
Ajay P Karnalli

Technology Transfer (TT) is vital action from drug development in Research and Development (R and D) Department to commercial manufacturing till the product discontinuation. This review is an attempt to give an insight about the transfer of pharmaceutical product from R and D to production including necessary documents required to review the supporting documents and execution procedures in production shop floor. TT is considered effective, if there is a documented evidence that the process and its parameters, repeatedly results in desired product quality which was established upon during TT between the transferee and transferor. For the execution of TT process, expertise from different department such as Engineering, R and D, QA, process analyst and production are teamed. the transmission comprises of arrangements procured in these flows of improvement to achieve the quality as planned throughout manufacture.


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