Compliance Updates and Blog Posts

Understanding Compliance Document Management The Importance of Compliance Document Management in Business Key Benefits of Compliance Document…

Understanding the complex regulatory compliance landscape of the European Union’s (EU) pharmaceutical industry poses a significant challenge for companies aiming to remain compliant while ensuring […]

Over the years, requirements of medicine packaging have undergone significant changes, driven by advancements in technology, changes in consumer expectations and needs, and, most importantly […]

From a quality control perspective, Braille Inspection and accuracy play an important role as Braille is mandatory on pharmaceutical packaging all across Europe, and is strongly recommended by the FDA […]

After exploring various solutions on the market, Dempsey Corporation made the decision to incorporate GlobalVision into their quality control processes. to eliminate errors and fatigue caused by manual proofreading.

As we continue to process the historic decision of the United Kingdom to exit the European Union, commonly known as Brexit, its far-reaching implications continue to unfold across various sectors.

In the digital age, where data serves as the backbone of decision-making, business operations, and technological advancements, ensuring the integrity of data has become paramount.

In today’s digital age, information security has become an utmost concern for organizations and their customers. As cyber threats continue to evolve, businesses must prioritize safeguarding […]

This comprehensive guide provides detailed insights into FDA labeling requirements and ensures your organization not only thoroughly understands labeling guidelines, but also sets best practices […]

FDA labeling requirements vary from market, product, and commodity. Each product, depending on its intention of use, has its own set of requirements that manufacturers need to follow.

To ace FDA food label compliance reviews and ensure your labels are always approved, tap into the power of automation. Automated quality control is a comprehensive solution for your compliance needs […]

In today’s digital age, a new threat presents itself to businesses that are heavily reliant on data. Many data-driven organizations rely on data integrity to be able to conduct their business operations without issues.

Now more than ever, the demand for safe and effective medical drugs is increasing on a global scale. This means that regulatory affairs teams are working overtime to interpret, apply, and communicate […]

There’s a saying: “Winning isn’t everything; It’s the only thing.” In business however, before you can win, you have to first comply with regulations.

Of note, the Food and Drug Administration (FDA) has official data integrity guidelines, out in full force as we speak. However, firms who are already following current Good Manufacturing Practices (cGMP) have nothing to worry about.

Still in its relative infancy as a discipline, regulatory affairs was created to meet a pressing need, regardless of the industry in question.

What is the FDA? The Food and Drug Administration is a government agency that operates under the United States Department of Health and Human Services.

One way companies can ensure high-quality standards is by demonstrating to accredited organizations that they can fulfill specific QMS requirements.

Every company needs change, but in the midst of implementing it, only a few of them think about ISO 9000. It is mostly perceived as a purely technical standard that only specific industries have to deal with […]

The pharmaceutical marketplace has changed dramatically over the last few years as pharmaceutical companies are moving from centralized, internal production to single-source […]