Analytical method verification according to USP 1226
As a pharmaceutical manufacturer, you want to check your analytical methods in accordance with USP 1226
What is method verification ?
Analytical method verification is a crucial process in laboratories and regulated industries, such as pharmaceuticals, biotechnology and chemistry. In these fields it is essential to ensure that the methods used to analyze samples are reliable, accurate and appropriate for the specific use. Method verification is particularly important when a laboratory adopts an analytical method already validated elsewhere, or when there are changes in test conditions.
What is the purpose of a method audit ?
The aim of USP 1226 method verification for the pharmaceutical industry is to confirm that methods are well adapted to the specific laboratory environment, comply with strict regulatory standards and deliver high-quality results.
What does the USP 1226 standard say ?
USP 1226 guides laboratories on how to demonstrate that the performance of an established and validated analytical method can be reproduced in their specific environment. The main objectives are to ensure that the method is: 1/ Fit for purpose, 2/ Reliable, 3/ Conforms to the original validation criteria.
What are the steps required for USP1226 method verification
The method verification process follows methodical steps, starting with a review of the original documentation to understand the method’s capabilities and limitations. Secondly, a detailed plan is drawn up to define the parameters to be tested and how the tests will be carried out. Thirdly, a series of experiments is carried out for each parameter. Finally, the data collected is analyzed to evaluate the method’s performance.
FILAB can help you validate your methods in accordance with USP 1226
Why call on FILAB for USP 1226 method validation ?
For over 30 years, our FILAB laboratory has had the experience and specific analytical equipment to support companies in validating analytical methods in accordance with USP 1226.
FILAB also performs method validations according to various regulations and standards, including :
VALIDATION STANDARDS / METHOD VERIFICATION at FILAB
Method validation according to SANCO 30/30
Par ailleurs, FILAB vous accompagne également dans des services de pilotage de validation de méthode à distance selon l’USP 1226, et dans la formation de vos équipes à la validation de méthode selon l’USP 1226.
The positive aspects of FILAB
A highly qualified team
Responsiveness in responding to and processing requests
A complete analytical park of 2100m²
Tailor-made support
FAQ
Quand faut-il réaliser la vérification d'une méthode analytique selon l'USP 1226 ?
La vérification de méthode est nécessaire dans plusieurs circonstances :
- lorsque la méthode est adoptée pour la première fois dans un laboratoire
- lorsque la matrice de l'échantillon est différente de celle décrite dans la pharmacopée
- lorsque les équipements utilisés pour l'analyse diffèrent de ceux recommandés par l'USP
