Sampling standards keep managers of environmental monitoring (EM) on their toes. Read this blog to learn more about how to use high flowrate monitoring to make the most out of your EM practices in less time.
In the final part of our five part series of Quality Risk Management per Annex 1, we explore the benefits of a Cleanroom Process Risk Assessment and how our Contamination Control Advisers can provide you with one. Process Risk Assessment: Why it’s important A process risk assessment helps you to to ensure risks are properly […]
The use of Quality Risk Management (QRM) principles and risk-based approaches are prominent expectations throughout the Annex 1 draft. Risk-based approaches are mentioned 43 times in the draft reinforcing the importance of using Risk Based approaches in all aspects of sterile product manufacturing. Here we highlight requirements related to Quality Risk Management that are specifically […]
The use of Quality Risk Management (QRM) principles and risk-based approaches are prominent expectations throughout the Annex 1 draft. Risk-based approaches are mentioned 43 times in the draft reinforcing the importance of using Risk Based approaches in all aspects of sterile product manufacturing. In part 2 of our five part series, we highlight requirements related […]
In this blog series, we take a look at common terms and initial considerations for selecting an aerosol particle monitor for various applications.
Daniele Pandolfi, Global Product Line Manager, and Frank Panofen, Global Marketing Manager, discuss data management systems and the way they can better improve your process in the digital age.
Upgrading is a streamlined process made easy by the FacilityPro® system’s user requirement specifications (URSs) of data integrity, automation, simplicity, integration, service and support.
Following the last blog which discussed three categories of monitoring requirements, we move onto monitoring specifically for certification.
In questa serie di blog in sei parti, esaminiamo problemi comuni con il trasferimento, l’integrità, l’analisi, la reportistica e l’archiviazione dei dati che incontriamo ogni giorno come proprietari e utenti di camere bianche. Esploreremo come l’automazione e le soluzioni elettroniche, entro i parametri delle autorità di regolamentazione e del cGMP, possono contribuire a migliorare l’efficienza e la qualità dei prodotti.
Particle Measuring Systems (PMS) Italy will exhibit at Pharmintech, from 13 to 15 April 2016 in Bologna.
Returning for its 15th anniversary, Pharmintech is the international event dedicated to the pharmaceutical, parapharmaceutical, personal care and nutraceutical industries. With over 350 exhibitors last year coming from all around the world, this show gathers the breadth of the international supply chain for the pharmaceutical industry.