what is the defination of calibration & verification?

Answer Posted / pankaj pawar

Calibration is simply the process of comparing the unknown with a reference standard and reporting the results. For example:
Applied= 1.30V, Indicated= 1.26V (or Error= -0.04V)
Calibration may include adjustment to correct any deviation from the value of the standard.

Verification, as it relates to calibration, is the comparison of the results against a specification, usually the manufacturer's published performance figures for the product. (e.g. Error= -0.04V, Spec= ±0.03V, "FAIL"). Some cal labs include a spec status statement on their Certificate of Calibration. (i.e. the item did/did not comply with a particular spec).

Is This Answer Correct ?    5 Yes 0 No



Post New Answer       View All Answers


Please Help Members By Posting Answers For Below Questions

how to decide for one product require water content or LOD?

323


what is mean by extactable and leachable study?

557


what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.

2188


on the basis of bcs class how to proceed the solubility?

271


How you develop a method in HPLC?

2071






How would you decide dissolution medium for NCE compound of class I drug

1690


CAN WE DETERMINE THE PEAK PURITY IN GAS CHROMATOGRAPHY ANALYSIS?

693


how to calculate elemental impurities?

534


My question about gas chromatography sulfur chemiluminsecence detector. I test unknown sample gas by GC-SCD (calibrated ) and the result of *H2S is 279 PPM , *but when I test the same sample with the GC-TCD (calibrated ) the value of *H2S is 2500 PPM . I'd like to inform you that both GCs are calibrated and have very good operation conditions with stable parameters . the question is if the sample gas with higher H2S over detection limits of SCD detector (1000 ppm). why the result it 279 ppm Best regards

1103


Qc interview questions

1242


4. Describe the operation of the Craig apparatus. Chapter.3 Equilibrium Processes in Separations

2148


Why we check moisture,ash & AIA in product

1393


what is definition of validation? which components are followed give detail?

1825


which are the sizes of capsules?

394


what is mean by dissolution biowaiver study?

318