The Ultimate Resource on Compliant Weighing in Pharma Production

Weighing applications in pharma manufacturing can strongly influence final product quality. However, regulations and standards such as GMP and ISO usually leave much to interpretation. This portal provides an overview of relevant standards and regulations for weighing devices and offers a range of knowledge tools such as white papers, guides and webinars that can help you comply with regulations more easily and efficiently.

Key Regulations and Standards for Weighing Processes

Understanding regulations, weighing processes, weighing technology and metrology is essential to ensure regulatory compliance over the lifetime of a scale. Let's take a look at some of the key regulations as defined by Good Manufacturing Practices (GMP), for example FDA, EMA, WHO, and ISO, that must be met by weighing processes in pharmaceutical production.

 



Regulatory Compliance of Weighing Processes in Pharma Production

Get an overview of the regulatory landscape related to weighing processes and find out which challenges those regulations pose to producers. Understand how weighing systems should be selected, installed and validated and how verification procedures should be established.


Download the White Paper

 Watch the Webinar
Weighing Equipment Selection
Weighing Equipment Design and Construction
Performance Verification of Weighing Equipment
Qualification and Validation of Weighing Processes
Ensuring Weighing Data Integrity