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Showing 1 - 11 of
11 matches in All Departments
Introduces Intelligent IoT as applicable to key areas towards smart
healthcare Discusses computational intelligence and IoT based
optimizations of smart healthcare systems Explores effective
management of healthcare systems using dedicated IoT based
infrastructures Includes dedicated chapters on securing patient's
confidential data Reviews diagnosis of critical diseases from
medical imaging using advanced deep learning-based approaches
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Etnia E Malocclusione
Angad Sharma, Deepak Kumar Gupta, Arun K. Garg
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R1,622
Discovery Miles 16 220
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Ships in 10 - 15 working days
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Etnia E Maloclusão
Angad Sharma, Deepak Kumar Gupta, Arun K. Garg
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R1,622
Discovery Miles 16 220
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Ships in 10 - 15 working days
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Ethnicité Et Malocclusion
Angad Sharma, Deepak Kumar Gupta, Arun K. Garg
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R1,623
Discovery Miles 16 230
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Ships in 10 - 15 working days
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Ethnicity and Malocclusion
Angad Sharma, Deepak Kumar Gupta, Arun K. Garg
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R1,618
Discovery Miles 16 180
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Ships in 10 - 15 working days
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Present investigation was undertaken to study the seroprevalence,
colicin production, identification and characterization of fimbrial
antigens of E.coli associated with calf diarrhoea. During the
course of study, a total of 146 faecal samples were obtained from
diarrhoeic calves of different age groups from various dairy farms
of Bikaner and processed for the isolation and characterization of
E.coli.
Validation is defined as the establishing of documented evidence
which provides a high degree of assurance that a planned process
will consistently perform according to the intended specified
outcomes. Validation studies are performed for analytical tests,
equipment, facility systems such as air, water, steam, and for
processes such as the manufacturing processes, cleaning,
sterilization, sterile filling, lyophilization, etc. There will be
a separate validation for the lyophilizer as an equipment item and
for the lyophilization process; for the cleaning of glassware and
the cleaning of the facility; and for the sterilization process and
for the sterility test. Every step of the process of manufacture of
a drug product must be shown to perform as intended. Validation
studies verify the system under test under the extremes expected
during the process to prove that the system remains in control.
Once the system or process has been validated, it is expected that
it remains in control, provided no changes are made. In the event
that modifications are made, or problems occur, or equipment is
replaced or relocated, revalidation is performed.
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