Q-REX: your modular platform for on-demand quality reporting
In addition to the regulatory obligation for traditional PQR/APR reporting, both the EMA and FDA emphasize the implementation of ongoing/continued process verification as integral part of validation activities throughout the product life cycle. The effort for the timely preparation of related quality reports is immense since many manual and thus error-prone activities are involved in the data acquisition, statistical analysis and the final compilation of validated documentation.
We are addressing this topic and have kicked-off the development of a modular software platform for on-demand quality reporting. Our vision is to contextualize, orchestrate and transform your quality-relevant data into GMP-compliant quality reports – automatically and with just one click. You will benefit from the simplified generation of quality reports like PQR, APR, OPV and CPV, while getting rid of manual processes and data integrity issues.
Free web seminar: How to turn the obligation of quality reporting into an opportunity
Learn more in our free live web seminar “How to turn the obligation of quality reporting into an opportunity” on 28 October at 4 PM CET, held by Dr. Andreas König, Managing Director at Quality König GmbH, and Dr. Andree Ellert, Product Manager Software at Körber Pharma.
Become a pilot customer
We are looking for interested pilot customers for our new quality review software. Let’s fine-tune the product together – and benefit from numerous advantages such as a say in product design and development, a free feasibility study and a 50% discount for one subscription year.