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Find the latest content and resources from our team of experts to keep you in the know for all things quality and regulatory in the life science industry.
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The FDA gives the Center for Veterinary Medicine (CVM) authority to approve new animal drug applications, issue ...
In industries such as life sciences, manufacturing, and healthcare, maintaining high standards for quality and ...
Innovation in medical technology is crucial for advancing healthcare and improving patient outcomes. However, the ...
When developing a new animal drug, the National Environmental Policy Act of 1969 (NEPA) requires sponsors to ...
One of the key frameworks in the pharmaceutical industry is GAMP 5 (Good Automated Manufacturing Practice). ...
Attending the ISPE (International Society for Pharmaceutical Engineering) Annual Meeting is always a highlight of ...
Water is one of the most commonly used ingredients in the pharmaceutical and biotechnology industries, but not ...
In the life sciences industry, quality is often seen as a regulatory requirement rather than a strategic business ...
The Drug Supply Chain Security Act (DSCSA) represents a significant step forward in enhancing the safety and ...
Endotoxin testing is a critical safety procedure used in pharmaceutical, biotechnology, and medical device ...
PCR (Polymerase Chain Reaction) tests have become widely recognized due to their essential role in detecting viral ...
When developing medical devices, clinical trials are a crucial step in determining safety and effectiveness. These ...
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