Blog

Oct. 22, 2011

FDA medical device classification involves placing items into certain categories according to how safe they are. This is very important to the health care industry because the lives of those affected by these devices should be protected.

Oct. 12, 2011

OTC drugs are the most common forms of self-medication in the US. Since they are offered over the counter they do not require the client to present a doctor's prescription. Some people argue that this might be a rather unsafe procedure since after all these products are still drugs which need to be taken with care.

Sept. 9, 2011

When it comes to football, defense matters. When it comes to planning a tailgate party, a good defense against foodborne illness matters even more.

Aug. 31, 2011

Food that is bought, sold, and imported in the United States needs to have a label, ingredients that are permissible, food facility registration. Many companies do not have the expertise and skills in creating labels, so they hire a FDA consultant in order to keep within compliance of the regulations.

July 6, 2011

As you may already know Import Alerts, or FDA's automatic detention lists, can cause serious issues for your clients. Import Alerts are also known as detention without physical examination.

May 2, 2011

Under the FDA food law known as the Public Health Security and Bioterrorism Preparedness and Response Act of 2002 food facility registration is required to certain food facilities as well as providing FDA advanced notice of shipments carrying imported foods.

March 5, 2011

Under the FDA laws a cosmetic is defined by its intended use, as “articles intended to be rubbed, poured, sprinkled, or sprayed on, introduced into, or otherwise applied to the human body…for cleansing, beautifying, promoting attractiveness, or altering the appearance.