With the maturation and application of genetic engineering technology, it is now possible to design, modify, and express proteins as needed, leading to a diverse array of recombinant proteins.

Aseptic processing demands reliable, robust, and validated analytical methods to ensure sterility, safety, and quality, ...

The purpose of this course is to provide candidates with some practical tools for validation - including qualification, process validation and analytical method validation. Validation is a regulatory ...

The Workshop is planned to highlight, review, and discuss issues related to the implementation of XRF methodologies, including addressing recommendations for compliance to technical requirements of ...

Analytical quality control refers to all those processes and procedures designed to ensure that the results of laboratory analysis are consistent, comparable, accurate and within specified limits.

In-line UV spectroscopy allows real-time monitoring of cleaning processes, enhancing process control and compliance with Pharma 4.0 goals. The method provides continuous detection of residual cleaning ...

In today’s pharmaceutical environment, where compliance and speed-to-market are paramount, analytical method development and validation play a foundational role. From early research through to GMP ...

Over the last 20 years the Nuclear Science and Instrumentation Laboratory (NSIL, formerly NSAL and Instrumentation Unit) has played a leading role worldwide in the effective use of nuclear ...