[Date Prev][Date Next][Thread Prev][Thread Next][Date Index][Thread Index]
[dvd-discuss] Thompson v. Western States Medical Center
- To: dvd-discuss(at)cyber.law.harvard.edu
- Subject: [dvd-discuss] Thompson v. Western States Medical Center
- From: "Arnold G. Reinhold" <reinhold(at)world.std.com>
- Date: Tue, 30 Apr 2002 09:18:17 -0400
- Reply-to: dvd-discuss(at)cyber.law.harvard.edu
- Sender: owner-dvd-discuss(at)cyber.law.harvard.edu
Here is a quote from Justice O'Conner's majority opinion, released
yesterday, in Thompson v. Western States Medical Center, which struck
down a ban on pharmacists advertising drug compounding services. Her
logic seems directly applicable to the DMCA's ban on dissemination as
applied in the DeCSS case. See especially the last two sentences.
"Several non-speech-related means of drawing a line between
compounding and large-scale manufacturing might be possible here.
First, it seems that the Government could use the very factors the
FDA relied on to distinguish compounding from manufacturing in its
1992 Compliance Policy Guide. For example, the Government could ban
the use of ³commercial scale manufacturing or testing equipment for
compounding drug products.² Compliance Policy Guide, App. to Pet. for
Cert. 76a. It could prohibit pharmacists from compounding more drugs
in anticipation of receiving prescriptions than in response to
prescriptions already received. See ibid. It could prohibit
pharmacists from ³[o]ffering compounded drugs at whole-sale to other
state licensed persons or commercial entities for resale.² Id., at
77a. Alternately, it could limit the amount of compounded drugs,
either by volume or by numbers of prescriptions, that a given
pharmacist or pharmacy sells out of State. See ibid. Another
possibility not suggested by the Compliance Policy Guide would be
capping the amount of any particular compounded drug, either by drug
volume, number of prescriptions, gross revenue, or profit that a
pharmacist or pharmacy may make or sell in a given period of time. It
might even be sufficient to rely solely on the non-speech-related
provisions of the FDAMA, such as the requirement that compounding
only be conducted in response to a prescription or a history of
receiving a prescription, 21 U. S. C. §353a(a), and the limitation on
the percentage of a pharmacy¹s total sales that out-of-state sales of
compounded drugs may represent, §353a(b)(3)(B).
The Government has not offered any reason why these possibilities,
alone or in combination, would be insufficient to prevent compounding
from occurring on such a scale as to undermine the new drug approval
process. Indeed, there is no hint that the Government even considered
these or any other alternatives. Nowhere in the legislative history
of the FDAMA or petitioners¹ briefs is there any explanation of why
the Government believed forbidding advertising was a necessary as
opposed to merely convenient means of achieving its interests. Yet
³[i]t is well established that Œthe party seeking to uphold a
restriction on commercial speech carries the burden of justifying
it.¹² Edenfield v. Fane, 507 U. S., at 770 (quoting Bolger v. Youngs
Drug Products Corp., 463 U. S. 60, 71, n. 20 (1983)). The Government
simply has not provided sufficient justification here. If the First
Amendment means anything, it means that regulating speech must be a
last‹ not first‹resort. Yet here it seems to have been the first
strategy the Government thought to try."
http://www.supremecourtus.gov/opinions/01pdf/01-344.pdf
Arnold Reinhold