Hi, Soapbuddy, and thanks for the response. Sorry I've been absent from the forum for the past few days.
I'm trying to learn as much as I can about the FDAGA, but I'm sure there are gaps in my knowledge. The 2009 draft seems to be an improvement over the 2008 draft. The 2008 version was downright horrifying. I read that the 2009 draft does away with 2008's annual fee of anywhere from $2,000 - $12,000, which is good. That alone would do lots of folks in -- some of us don't make $2,000 in an entire year and can't afford to put up that kind of money just for the privilege of being in business.
I'm a bit confused about what the 2009 draft says about Good Manufacturing Practice adherence (
http://www.fda.gov/Cosmetics/GuidanceCo ... efault.htm). I've read that it is not mandated, but I don't know if that's correct. I've also read that the door may be open for GMP regulations in the future. It would be good if special GMP consideration was given to small businesses. Good manufacturing practice sounds like a good thing, and a lot of it is. GMP includes some common-sense kind of stuff that most of us already do anyway -- keep your work area clean, keep "filth" out of your product, store supplies properly, etc. But what home-based, sole proprietor business could possibly comply with the testing guidelines outlined under "Raw Materials" and "Laboratory Controls"?
The main concern, it seems, is that Congress has no idea how small businesses are run (particularly tiny home-based ones like a lot of us have) and may strangle these businesses with burdensome albeit well-intentioned red tape. Even if fees are dropped and GMP guidelines are relaxed, registering your business annually, submitting ingredients lists for everything, and reporting and this, that, and the other creates a bureaucratic quicksand that could suffocate small businesses. The paperwork pile is big enough as it is, and this just adds to it. A small business would be too busy juggling all of its paperwork to find the time to actually produce its products!
What about folks that just make soap? Will they be affected? The FDA does not regulate soap so long as it is strictly soap and makes no therapeutic claims, correct? Say your soap is “moisturizing” or clears up acne, or has some sort of aromatherapeutic benefit, though, and now you’re treading into FDA territory and would be subject to the FDAGA, if I'm not mistaken. Even though I make only soap, I am still concerned about this bill because there are so many wonderful folks that make and sell lotions and lip balms and all other kinds of good stuff and it makes me ill to think that they might get regulated out of business. My fear is that someday only giant corporations will be able to afford to stay in business.
I hope there will be some sort of small business exemption, or at least language in the bill that recognizes the unique challenges of the small, often home-based, business.