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ISO 9001:2015

Analytical Method Validation & Verification

Analytical method validation parameters will be executed as per current regulatory guidelines & Pharmacopoeias (e.g. ICH/ANVISA/USP/Ph.Eur./BP/JP/IP)
  • Specificity
  • Limit of Detection & Limit of Quantification (LOD & LOQ)
  • Linearity & Range
  • Precision (System Precision, Method Precision & Intermediate Precision)
  • Accuracy
  • Robustness
  • Solution Stability
validation
Aashtha Training Center

Certificate Course is benefited to get Job in Quality Control (QC) department and Analytical Development Lab (ADL) in
Pharmaceutical Industries & Chemical industries.

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Get In Touch

Let’s talk

+91 94278 07635
+91 99099 28065
info@aashthaanalytical.com

TF-05/06, Third Floor, Raama Esquire, Gotri, Vadodara-390021, Gujarat, India
Contact us
Aashtha Training Center

Certificate Course is benefited to get get Job in Quality Control (QC) department and Analytical Development Lab (ADL) in Pharmaceutical Industries & Chemical industries.

Navigation

Get In Touch

Let’s talk
+91 94248 07635
+91 99099 28065
info@aashthaanalytical.com
TF-05/06, Third Floor, Raama Esquire, Gotri, Vadodara-390021, Gujarat, India
Contact us
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