GMP Label & Compliance Articles

Quality determines whether a medical device performs safely, reliably, and in compliance with regulatory expectations. Every aspect of development and manufacturing must be controlled to prevent defec … read more

Cleanrooms play a vital role in medical device manufacturing by reducing the risk of contamination during production. To meet FDA and ISO requirements, manufacturers must follow GMP standards that tig … read more

Cryogenic storage plays a critical role in preserving sensitive biological materials, pharmaceuticals, and medical specimens. Whether you're managing a biobank or working in a pharmaceutical manufactu … read more

The U.S. Food and Drug Administration (FDA) enforces strict labeling and packaging regulations to protect consumers and uphold product quality. Non-compliance can lead to recalls, legal penalties, and … read more

Introduction to OSHA Labeling Requirements Workplace safety is a top priority in any industry handling hazardous chemicals. The Occupational Safety and Health Administration (OSHA) sets strict guideli … read more

Label compliance is the process of meeting regulatory and industry standards for product labels. It ensures labels are accurate, clear, and durable, providing the necessary information for safe use, t … read more

Understanding Pharmaceutical Labeling RequirementsPharmaceutical labeling requirements ensure patient safety, regulatory compliance, and product integrity. Key regulatory authorities, such as the FDA … read more

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