Establishing and Validating the Lifecycle of Cleanroom Gowning
Cleanroom environments demand rigorous contamination control with gowning protocols playing a pivotal role in safeguarding product integrity and operator safety....
Cleanroom environments demand rigorous contamination control with gowning protocols playing a pivotal role in safeguarding product integrity and operator safety....
One critical question remains central to precision printing: 'How much ink is actually being deposited on a product’s surface during...
Leak testing for cold chain and terminally sterilised products presents unique challenges due to factors such as condensation and entrapped...
Applying identification on solid dosage drug products can be necessary from the point of regulatory compliance, patient safety and brand...
Tablet imprinting is sometimes necessary for ensuring precise identification, brand differentiation and regulatory compliance. However a tablet’s shape, dimensions and...
The revised Annex 1 guideline, released in August 2022, includes specific requirements related to container closure integrity. Clause 8.24 states:...
At the recently concluded PMEC 2024, our booth attracted significant visitor interest by showcasing innovative solutions addressing Annex 1 compliance...
Image Credits: DALL.E Fill-finish and lyophilization are essential processes in the pharmaceutical industry, particularly for protecting sensitive drug formulations. Fill-finish occurs...
In critical fill-finish sterile areas, even the smallest particles and fibers can cause significant contamination issues endangering the finished injectable...