Taking a Stand Against The FDA Globalization Act 2008
Four
Industries. One Bad Law. In today's cosmetic industry, there is no more
pressing issue than the FDA Globalization Act of 2008. For this
industry, it's the wrong policy and the wrong law during this
challenging economic time. Industry leadersare taking a stand against the Discussion Draft of
the Food and Drug Administration Globalization Act of 2008 in hopes
that it does not pass.
New York, NY (PRWEB) October 5, 2008 -Four Industries. One Bad Law.
In today's cosmetic industry, there is no more pressing issue than the
FDA Globalization Act of 2008. For this industry, it's the wrong policy
and the wrong law during this challenging economic time. Industry
leaders are taking a stand
against the Discussion Draft of the Food and Drug Administration
Globalization Act of 2008 in hopes that it does not pass.
Important in understanding why so many cosmetic
companies are protesting this act, one must take into consideration
that the cosmetic industry falls under the same administrative umbrella
as food, drugs and drug devices. Basically, if one party falls under
scrutiny, it negatively affects the other 'sibling' branches. The FDA
Globalization Act of 2008 was triggered by the food crisis' that
occurred that year which brought the food industry under examination
when this "sibling" fell under hardship. While the cosmetic industry
could use some discipline, the provisions of the FDA Globalization Act
do not address the issues most important to remedy the problems in the
cosmetic industry: the loop holes that allow fragrance chemicals and
"processing aids" to go unlisted on the ingredient lists. According to
the rules set in place by the FDA, all ingredients must be listed in
order of predominance on a cosmetic ingredient list EXCEPT ingredients
that give a product an odor. Because of this loop hole, the word
'fragrance' may represent many hundreds of ingredients in one product.
Therefore, a product that contains fragrance chemicals can be labeled
'unscented' or 'fragrance-free'.
At the end of the day, the provisions listed by the FDA Globalization
Act add fees and increased administrative work to the cosmetic industry
which goes toward fixing the problems of its "siblings" in the food
industry, but bring no benefit or reform to the cosmetic industry. The
fact is the conditions contained in the draft of the FDA Globalization
Act do not address any of the challenges faced by the cosmetics
industry today. Instead, they focus on adding burdensome and
unreasonable fees and incredibly labor intensive paperwork that are
really designed to send a "tsk-tsk" to our siblings. They do nothing to
protect consumers, which is the stated intent of the cosmetics laws.
In a nutshell the FDA Globalization Act of 2008 in current form will require: **$2000
yearly registration fee for all companies engaged in manufacturing,
processing, packing or holding cosmetics in the United States.
**$10,000 yearly registration fee for all companies that import ingredients or finished cosmetics.
**$12,000 yearly registration fee for all companies that import ingredients, manufacture, process or hold cosmetics.
**The administration of the requirements of the FDA will require
companies to have at least one person working full time on staying
compliant. This will cause many one person operations to go out of
business and raise the price of cosmetics industry wide to pay for the
new person or entire department depending on the size of the company.
**Require that a facility that manufactures cosmetics to report to the
Secretary all anticipated and unanticipated serious adverse events
relating to the use of cosmetics it has manufactured. In reality if a
company anticipates adverse events they would not put out the product
and how can they plan for an unanticipated event.
**Included hidden fees not yet discussed including; re-registration
fees, re-inspection fees, certification fees, certifying agent
accreditation, laboratory accreditation, export certification and
importer registration.
**It will create a system that makes cosmetics as expensive as drugs and you know what that means…consumers pay the price
FDA Globalization Act of 2008 in the current form will:
**Shut down free trade with countries now dependent on the cosmetic
industry. Natural ingredients are sourced from countries around the
world because they grow only in those regions. A great example of an
ingredient that is enjoyed by millions of Americans is Shea Butter. It
grows abundantly in Africa and small villages around Africa sell their
Shea Butter directly to small businesses all over America. With this
legislation the livelihood of the American company and the African
village will be shut down.
**Shut down existing small and medium sized cosmetic companies that
cannot afford the YEARLY registration fee. Many companies will be shut
down over night by the fees and others will not last through the year
once they pay the fee and now must hire additional employees to process
the additional administrative work.
**Shut down the stream of new companies started with a dream, a
passion, and a shoe string budget started around the kitchen table. How
many success stories started right there? Thousands of them started
just there. Even many of the giant corporations today started with one
or two people who had a vision to make a difference in their industry.
FDA Globalization Act of 2008 will NOT: **Make cosmetics
safer. There is nothing in the language of the FDA Globalization Act of
2008 that will make cosmetics safer to the American people. It will not
change labeling laws or disclose loop holes that currently allow
fragrance chemicals to be undisclosed.
Granted this is just a 'draft' at the moment, not a formal bill,
nevertheless it is moving in that direction. Industry leaders are petitioning and making trips to Washington DC to advocate against the passage of the FDA Globalization Act.
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