GMP Label & Compliance Articles

In a recent blog post, we covered the importance of calibration for the medical device industry. But an important question remains - what is equipment calibrated against? In order to ensure that equip … read more

If you manage a medical device manufacturing operation, you are intimately aware of the importance of equipment uptime and meeting production schedules. Unplanned downtime of critical manufacturing eq … read more

Selecting the right thermal transfer ribbon type is essential for ensuring the durability, print quality, and longevity of your labels. Whether you need labels to withstand harsh environments or serve … read more

Overview of 21 CFR Part 80121 CFR Part 801 outlines FDA labeling requirements for medical devices sold in the U.S. These regulations ensure that all devices have clear, accurate instructions, warnings … read more

The performance and safety of medical devices depend heavily on consistent accuracy, which is why the process of equipment calibration is a critical component of quality control and regulatory complia … read more

Recent Regulatory Changes for Cannabis Packaging in CaliforniaIn 2024, California introduced several key updates to its cannabis packaging regulations, affecting businesses across the supply chain, in … read more

Good Manufacturing Practices (GMP) regulations serve as the compass guiding the pharmaceutical and medical device industries toward quality, safety, and compliance. Among the critical elements of GMP … read more

The FDA maintains the Good Manufacturing Practices (GMP) Standard for companies manufacturing medical devices, pharmaceutical, biotechnology, and other healthcare related products. The GMP standard is … read more

In 2012, the United States officially adopted GHS standards when OSHA updated their Hazard Communication Standard to align with the Globally Harmonized System of Classification and Labeling of Chem … read more