The FDA first began approving drugs and medications as being safe for consumption in 1939. However, there’s still the question of whether or not something is really FDA approved for some people. The last thing they want is to take a medication or drug that may damage their health.
Knowing – for sure – if something is approved by the U.S. Food and Drug Administration is a big deal. While some marketers make the claim they are FDA approved, there are some less-than-trustworthy companies out there.
The FDA is responsible for protecting public health by regulating biologics, medical devices, human drugs, animal drugs, cosmetics, food and any electronic product that emits radiation. However, not all these products undergo the premarket approval process by FDA experts.
Keep in mind, there are some companies that utilize the services of third party services, such as EMMA International: Leading FDA Compliance Consultant, when seeking this approval, which is fine. The problem arises when a company begins to sell a product before actually receiving approval.
Here you can learn more about the role of the FDA and how to tell if a product has really been approved as safe for consumption or use.
Companies Don’t Receive FDA Approval
One of the first things you should understand is that no company is going to receive FDA approval. This includes manufacturers, laboratories or health care facilities. The FDA doesn’t have the authority to inspect these facilities to verify that they are in compliance with good manufacturing regulations.
Operators and owners of both domestic and foreign drug, device and food facilities have to register the facilities with the FDA unless there is some type of exemption in place. Tissue and blood facilities also have to register with the agency.
The FDA Approves New Biologics and Drugs
While the FDA doesn’t provide approval for specific companies, it does for certain biologics and drugs. In fact, new drugs must receive FDA approval before being marketed in interstate commerce.
Some of the biologics that need FDA approval include blood products, blood, cellular therapies, vaccines and therapeutic proteins. Additionally, manufacturers have to prove they can make a drug product based on the federal quality standards.
The FDA doesn’t test or develop products prior to approving them. Instead, the organization reviews the results of testing done by manufacturers. If the FDA has actually granted approval, then it means that the agency has determined that the advantages of the product, medication, food, etc. outweigh the risks for the items intended use. It’s a good idea to look at the director of both approved and unapproved finished drugs on the market today before taking anything new.
FDA Approval is More Important than You May Think
While it can be challenging at times to determine what’s FDA approved and what’s not, there are resources out there to help, such as the one mentioned above. If you are given a new medication or one is recommended to you, be sure to do your due diligence to only use items that have been approved. In the long run, this will help you and your family remain safe and healthy.
Being informed is the best way to know if something is safe. So always make sure to do your homework and determine what you should and should not consume or take.
Article Submitted By Community Writer