The conversation around genetic engineering and food is undermined by a lack of information that breeds confusion and distrust. Consumers feel misled. Scientists feel misunderstood. Public officials ...

The medical device industry is evolving and expanding with every passing year, with new devices being developed to save lives and treat an array of ailments and health conditions. At the same time, ...

Laura Johnson, senior director, sales, life sciences, Loftware, discusses scenarios where unclear labeling led to challenges for patient outcomes. Drug labeling has become a key issue in the ...

EMA is under pressure to exert even tighter standards on biosimilars being marketed in Europe. The European Medicines Agency (EMA) has reached a key stage in the lengthy process of creating a ...

Each year when federal statistics are released, it comes as little surprise that violations of OSHA's Hazard Communication Standard are among the top 10 safety citations issued to general industry.

Medical device labeling is considered as important as classifying a product or creating an insulation diagram. In IEC 60601-1, labeling is deemed "a critical component of a medical device." 1 The ...

When OSHA performs an on-site inspection of a facility, it should be a nonevent, yet the trend these days is moving toward more citations, greater penalties, and more frequent inspections. Further ...

The ability to engineer and observe fluorescently labeled proteins inside living cells has had a profound impact on biological research. However, although every microscopist is thrilled by the ability ...

Senate Agriculture Committee leaders have released a new federal mandatory labeling bill for genetically engineered food. These Senators are trading a state mandatory labeling law for a federal ...