OUTSOURCE! belongs to the Contract Laboratory Network
Advertisement
Clinical Laboratory Improvement Amendments, more commonly known as CLIA, are federal regulations (in the US) that apply to any clinical laboratory that performs testing on humans, with the exception of clinical trials and basic research. A clinical laboratory...
Cosmetics sold in the United States need to be in compliance with labeling requirements of the Federal Food, Drug, and Cosmetic (FD&C) Act, the Fair Packaging and Labeling (FP&L) Act, and Food and Drug Administration Regulations. These laws require...
SAE standards play a crucial role in various testing processes, from the initial design phase to the final product validation.
Understanding the Importance of California Proposition 65 Testing for Products Sold in California
Good Laboratory Practices (GLP) regulations are essential for ensuring the quality, integrity, and reliability of non-clinical laboratory studies.
Proper labeling helps consumers make informed choices, manage dietary needs, and avoid allergens.
The Office of Chemical Safety and Pollution Prevention (OCSPP) test guidelines ContractLaboratory.com received a request from an Organics Gardening Company needing an Agriculture laboratory for EPA Pesticide Testing of a new pesticide they are registering with the...
The US FDA recently announced it would be making changes to the way it enforces the Food Safety Modernization Act (FSMA) of 2011, an act meant to help ensure the safety of the food supply. The agency is calling the act the biggest food safety overhaul in 70 years....
Industrial hygiene is the science relating to the health and safety of employees in the workplace. Using environmental monitoring, industrial hygienists develop new methods and practices to help mitigate potential hazards. Hygienists analyze hazards that can cause...
For feed manufacturers, investing in lab testing is not just about meeting regulatory requirements—it's about delivering high-quality products that consumers can trust.
Are you curious about how vaccines are made? Or about the research and time that goes into their development? The U.S. Food and Drug Administration’s Center for Biologics Evaluations and Research, CBER for short, is the organization in the United States that...
What is REACH registration, and what type of testing must be done for REACH registration? REACH (Registration, Evaluation, Authorization and Restriction of Chemicals) is a regulation set forth by the European Union, that began in 2007. It was started as a way to...
A NATO STANAG (STANdardization AGreement) is a standardization document specifying an agreement among member nations to implement a specific standard. The NATO STANAG sets the parameters for procedures, processes, terms, and conditions for military and other...
In the third annual "Chain Reaction" report, the most popular US fast food chains are graded on their use of antibiotics in food, specifically meat, as well as their policies and meat sourcing practices. Historically, antibiotics have been given to animals that...
Food safety is a critical concern for consumers, manufacturers, and regulatory bodies alike. One of the essential aspects of food safety is ensuring that food contact substances (FCS)—materials that come into direct contact with food—are safe and do not pose health...
Advertisement
As parents and guardians prepare their children for the new school year, one...
The integrity of the Olympic Games relies heavily on the principles of fair...
Advertisement
Advertisement