Product and labeling mix-ups can result in potentially serious consequences and are one of the top causes of recalls in the world. Therefore, manufacturers must pay particular attention and implement procedures to ensure that the correct medication and strength are in...
A benchmark survey with the goal was to identify what line clearance/change over best practices that will help overcome existing barriers and help transition the industry as a whole toward smaller batch sizes? Several best practice examples emerged from the benchmark...
The packaging of pharmaceutical products is regulated in most countries. Authorities expect that any printed information – such as product, use and storage data on the packaging material artwork or batch-specific data (e.g., expiration date) – is readable by the...
The introduction of Track and trace (T&T) regulations has driven specific changes to industry packaging practices. Digital information related to the drug has become a major quality-relevant part of the drug packaging process. Unique product identifiers must be...
Implementation and solutions overview from a packaging perspective The benefits of ePI are well understood and broadly accepted. This paper examines and responds to the challenge of developing ePI solutions that add value to patients and healthcare providers alike...
