[Congressional Record Volume 159, Number 161 (Wednesday, November 13, 2013)]
[Senate]
[Pages S7967-S7969]
From the Congressional Record Online through the Government Publishing Office [www.gpo.gov]
DRUG QUALITY AND SECURITY ACT
Mr. MARKEY. Madam President, I wish to begin by thanking Chairman
Harkin, Ranking Member Alexander, Senators Franken and Roberts, and all
of their staffs for their tremendous leadership on this bill. This bill
was also developed in concert with our counterparts in the House of
Representatives. I extend my thanks to ranking member Henry Waxman and
chairman Fred Upton and their staffs of the Energy and Commerce
Committee. What we have now is a bipartisan, bicameral bill that
addresses two very serious issues: the safety of compounded drugs and
the security of our entire drug supply.
Last fall an outbreak of fungal meningitis stunned the Nation and
thus far has claimed the lives of 64 people and has sickened 751 in 20
States. This issue hits home for me because it started in
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Massachusetts. At the center of this tragedy was the New England
Compounding Center, also known as NECC. It is located in Framingham,
MA. I met some of the victims of this terrible outbreak and heard about
their struggles, people like Jerry Cohen, a resident of Pikesville, MD,
who went to the doctor for routine steroid injections to treat
recurring back pain and received two doses that came from the
contaminated lots. Jerry suffered a stroke and had to adjust to a new
life, dealing with dizziness, nausea, weakness, and exhaustion. Melanie
Norwood's mother Marjorie went into a Tennessee hospital to treat an
acute back injury she suffered while mowing the lawn. Instead of
walking out of the hospital, Marjorie became severely sick, spent
months in the hospital and a nursing home, and now has permanent nerve
damage and medical bills that are close to putting her into bankruptcy.
For the last decade complaints about sterility, safety, lack of valid
prescriptions, and mass production of drugs have been lodged against
NECC. Yet the company was allowed to continue operating largely
unchecked, falling between the regulatory checks that exist between
Federal oversight of drug manufacturers and State oversight of
pharmacies.
Sadly, NECC was not an isolated instance. Almost a year ago I issued
a report detailing more than a decade of violations and problems at
compounding pharmacies all across our Nation. Contaminated IV
solutions, tainted steroid injections, and fouled eyedrops permanently
impacted thousands of patients' lives across this country and killed or
injured dozens across 34 States. The New England Compounding Center,
like many large compounding facilities, fell into a regulatory black
hole. That is because there are two kinds of compounding pharmacies:
the neighborhood pharmacist you have known and trusted for years and
the large drug manufacturers operating in the shadows that have slipped
through the regulatory cracks.
Traditional compounding pharmacies make custom medication that fits
the needs of an individual patient, such as creating a liquid
medication instead of a pill for an elderly patient or a child because
it is easier to swallow. We are familiar with that corner-store
pharmacist who does that for a patient. These pharmacies are an
important tool in our medical arsenal and have historically fallen
under the jurisdiction of the States. They are the corner pharmacies
that people grew up with. They are the corner pharmacies that people
trust.
But there has been a recent disturbing trend of larger compounding
pharmacies entering the market, making high-risk drugs sold to
hospitals and clinics throughout the country. These compounding
facilities are operating more as modern-day drug manufacturers rather
than the mortar-and-pestle compounders of yesteryear on the corner near
your home. They are not on Main Street, and they do most of their
business out of site and under the FDA's radar.
In 1997 Congress passed a law to define FDA's role in the oversight
of compounding pharmacies, but just 2 days before the new law was to
take effect seven compounding pharmacies sued to block its enactment.
Since then, the law and the FDA's authority to regulate compounding
pharmacies have been mired in litigation and uncertainty. The result is
that oversight of even large-scale drug manufacturers, such as NECC,
has been largely relegated to the States.
How are the States doing their job? Well, last April I issued an
investigative report that took a deep look at how States actually
oversee and govern the activities of compounding pharmacies. What I
found was a regulatory state of disarray. My investigation found that
nationwide most State regulators did not look at the safety of
compounding pharmacies. They do not make all their activities and
investigations public. Some of them did not even know how many
compounding pharmacies exist in their State, and States typically are
not equipped to regulate the safety of large companies shipping massive
quantities of drugs outside their own borders into States all across
our country.
Since the NECC outbreak, some States have made efforts to improve
their regulations and guidelines over compounding pharmacies, but the
results are not consistent. Within the last month my home State of
Massachusetts passed through its house and senate a bill that I am
proud to say will put in place the strongest State regulations in the
country overseeing the compounding pharmacy industry. However, while
Massachusetts has become a national leader in the oversight of
compounding pharmacies in the aftermath of what happened at NECC, this
does little to protect the residents of other States. It cannot protect
residents of Massachusetts from drugs that are shipped in from other
States that do not have strong safety standards in place.
The Drug Safety and Security Act in front of us today helps to solve
that problem by creating for the first time a national and uniform set
of rules for compounding pharmacies that wish to register with the FDA
and be subject to FDA oversight and enforcement. The bill also provides
transparency by requiring the FDA to publish a list of the name and
location of registered facilities that are compounding drugs in large
quantities without a prescription. The Drug Safety and Security Act
also mirrors several concepts from the VALID Compounding Act of 2013,
legislation which I introduced in the House of Representatives. The
bill distinguishes between compounders engaging in traditional pharmacy
work and those making large volumes of compounded drugs without
individual prescriptions. It places limits on the types and quality of
ingredients that can be used to compound drugs. It ensures that drugs
removed for the market for safety and effectiveness reasons are not
compounded. The bill requires reporting of adverse events, such as
patient sickness or hospitalizations that could be caused by
compounding pharmacies that are registered with the FDA. It provides
more information on the label of compounded drugs, including
identification of the drug as being compounded--the first time ever
that this information will be required.
Because of this bill, for the first time ever, the FDA will know who
these large sterile compounding entities are and what they are making.
The FDA will be given the resources it needs to conduct inspections of
those facilities. For the first time ever, hospitals and health care
facilities will have the option of purchasing compounded drugs that are
subject to rigorous FDA quality standards and oversight. Because this
bill removes the legal ambiguities of existing law, compounding
pharmacies will no longer fly under the radar. This bill will go a long
way in ensuring that public health is protected and compounded drugs
are safe.
I specifically thank Chairman Harkin and his staff for including in
this bill a provision that I authored requiring the GAO to examine
whether States and Federal authorities are doing their jobs to properly
ensure the safety of compounded drugs.
Congress needs to continue to keep a close eye on the FDA and this
industry, holding them accountable for their new responsibilities. This
study will assist us in carrying out effective oversight of this new
law. We need to ensure that a tragedy like the NECC meningitis outbreak
is never repeated.
With the passage of the Drug Safety and Security Act, today we have a
clear example of what Congress can accomplish when both sides come
together in a bipartisan fashion. We can protect the public, we can
hold industry to high but achievable standards, and we can support
small businesses that have been doing the right thing for years.
This is a very important, historic piece of legislation. It goes
right to the heart of what Congress can do to make sure that when drugs
are in interstate commerce, we are protecting people so that the health
of their families is, in fact, being protected. That is the essence of
what Congress should be doing.
It is a very good day when Congress is working to protect the people
of our country. Today is one of those days. Throughout the course of
this week we are going to have a discussion about the role the Federal
Government has to play in ensuring that the drugs which families in our
country use are, in fact, safe for their consumption, that the
representations that are made to those families are accurate. We cannot
accept a rollback of the protections,
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which did happen in this area. That exposed families to the kinds of
risks that generations ago were common within our country. It is a big
day. It is a historic piece of legislation. I urge its unanimous
passage through this body.
I yield the floor and suggest the absence of a quorum.
The PRESIDING OFFICER. The clerk will call the roll.
The legislative clerk proceeded to call the roll.
Mr. BLUNT. I ask unanimous consent that the order for the quorum call
be rescinded.
The PRESIDING OFFICER. Without objection, it is so ordered.
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