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Intelligent Internet of Things for Smart Healthcare Systems (Hardcover): Durgesh Srivastava, Neha Sharma, Deepak Sinwar, Jabar... Intelligent Internet of Things for Smart Healthcare Systems (Hardcover)
Durgesh Srivastava, Neha Sharma, Deepak Sinwar, Jabar H. Yousif, Hari Prabhat Gupta
R3,416 Discovery Miles 34 160 Ships in 12 - 19 working days

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

Unfold the Stories of Unsung Heroes Part II - Common People - Uncommon Stories: Ritish Sharma, Deepak Joshi, Aspiring Blog Unfold the Stories of Unsung Heroes Part II - Common People - Uncommon Stories
Ritish Sharma, Deepak Joshi, Aspiring Blog
R226 Discovery Miles 2 260 Ships in 10 - 15 working days
Process Validation of Ceftriaxone Sodium Dry Injection (Paperback): Shashank Tiwari, Deepak Sharma, Sharma Deepak Process Validation of Ceftriaxone Sodium Dry Injection (Paperback)
Shashank Tiwari, Deepak Sharma, Sharma Deepak
R1,262 Discovery Miles 12 620 Ships in 10 - 15 working days

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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