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All participants had been vaccinated for HBV (as per Canadian guidelines); hence, no new infection was found, and HBV sensitivity could not be computed.
The ITR formulation was found to be stable too as per ICH guidelines.
Further, this study is designed to validate the developed methods as per ICH guidelines.
Ethics committee approval was, therefore, not required for this purpose as per the institutional guidelines.
Mouse tissue samples were collected as per RIKEN Yokohama institutional guidelines.
A thorough and complete method validation of LS in human K3EDTA plasma was carried out, as per the USFDA/EMEA guidelines (USFDA bioanalytical guideline 2001 and EMEA bioanalytical guideline 2011).
Further investigations, including echocardiography, knee or hip x-rays, computed tomography of the brain, were conducted as per published guidelines.
As per the guidelines, dairy products, nuts, beans, and seeds have a high phosphorus protein ratio and should be avoided.
The workability of fresh SCGC was assessed by slump flow, V-funnel, L-Box and J-Ring test methods as per EFNARC guidelines.
The developed method was validated as per ICH guidelines.
The method was validated as per ICH guidelines.
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