Microbial Analytical Methods Qualification and Validation
Benefit from developing the analytical methods early in your product development stage, understand the basic methodology and utilize our prior experience to guide your method qualification choice.
With you on your biologics journey...
Why perform microbial microbial analytical methods validation and qualification?
Analytical method qualification is the first documented measurement of the method’s performance under the relevant guidelines and its scientific purpose.
Validation, however, demonstrates the analytical procedure’s suitability for its intended purpose by following pre-defined objectives gathered from development and qualification activities. During the early stages of product development, qualification can be sufficient. However, validation of the analytical methods is necessary when closer to the registration of the product.
3P´s analytical methods qualification and validation services
We produce standard operating procedures (SOPs) with system suitability testing (SST) and assay acceptance criteria during our analytical methods qualification activities and produce a method qualification report detailing the findings and justifying the conclusions. Data from the qualification study will be used in developing the criteria for validation, which requires a more stringent approach. Our approach to validation is to take pre-defined acceptance criteria for each method and follow relevant guidelines.
We prepare the validation protocol, which is followed by documenting all data and the acceptance limit of the method in all parameters required (including specificity, linearity, range, accuracy, precision, quantification, detection limit) according to the particular assay. These activities are performed within 3P’s quality system and require formal protocol, report, and SOP updates.
What we will deliver
We provide efficient analytical methods qualification and validation by utilizing our knowledge and expertise to provide all relevant documentation and support, allowing for further product development and approval.
Our dedicated team of specialists will be happy to discuss any of your Analytical Methods Qualification And Validation needs. Contact us on +34 948 346 480 or email withinus@3pbio.com
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It’s about our capacity and how we visualize and invest in the processes it takes to grow with you. An infrastructure built on an unmatched and shared commitment to ensuring your biologics journey makes a difference to those who need it.
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It’s about our capacity and how we visualize and invest in the processes it takes to grow with you. An infrastructure built on an unmatched and shared commitment to ensuring your biologics journey makes a difference to those who need it.
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It’s about our capacity and how we visualize and invest in the processes it takes to grow with you. An infrastructure built on an unmatched and shared commitment to ensuring your biologics journey makes a difference to those who need it.
