Executive Team
Board of Directors
Bus. Development
Global Operations
North America
Europe & Asia
Financial Data
Annual Report
Corp. Governance
TGA Certification
GMP Standards
Publications
News
CEO's Blog
Industry Links
|
News From Natural Alternatives International, Inc.
LeDoux: ‘Failure to Prepare
for GMPs Could Lead to
Very Unfortunate Outcomes’
Q&A with NAI chairman and CEO
If you’ve been around the supplement
industry, you likely know Mark
LeDoux, founder, CEO and chairman of Natural Alternatives International
Inc. (NAI). The company is a leader in the design, development and manufacture
of dietary supplements and operates
facilities in Southern California
and Lugano, Switzerland. A strong proponent
of the new good manufacturing
practices (GMPs) for supplements,
LeDoux was elected by his peers to
serve as chairman of the Council for
Responsible Nutrition (CRN) for the
next two years. Nutrition Business Journal interviewed LeDoux in late
2008.
NBJ: How do you foresee the down
economy impacting the supplement
industry in 2009, and how should
companies respond?
Mark LeDoux: I believe that managers
have to come to grips with four real-time
events. The fi rst is that access to credit
is constricted at best and almost impossible
for many industry participants to
obtain. This could trigger a series of potential
negative outcomes, and consolidation
is clearly one real possibility. Excessive
leverage is a recipe for failure, so
companies need to keep clean balance
sheets if they can.
Second, the consumer is being forced
to make very signifi cant value decisions
in the face of defl ation on a variety of
fronts. People are feeling poorer and,
in many cases, are justifi ed in feeling so
due to declining asset prices throughout
the economy. So, if we want to continue
to see consumer acceptance of our supplements,
we have to provide them with
well-made products that meet or exceed
their expectations at reasonable prices.
Third, purchasing managers need to understand
that the days of infl ation may
be behind us for some time and be able
to respond to defl ationary pressures in
the supply chain—or exploit them intelligently
when presented.
Finally, along with the economy, the
implementation of GMPs in the dietary
supplement space is going to have
profound impacts on industry participants—
all the way through the supply
chain. Failure to adequately prepare for
these audits may lead to very unfortunate
outcomes. Those companies that
have the capabilities to prepare for and
execute in compliance of these rules
should see their enterprises prosper.
NBJ: Is NAI feeling any effects of
the economy now in late 2008?
ML: Certainly. One of the great ‘unpredictables’
has come to pass in the
surge in valuation of the U.S. dollar and
the surge in the value of the Japanese
yen—simultaneously. This was unimaginable
even a year ago, and it is having
currency translation effects on foreign
earnings.
NBJ: How are you responding to
these economic changes?
ML: We have to protect the balance
sheet and reduce non-essential spending
where appropriate. This does not
mean, however, that we will reduce our
efforts to continue expanding current
and new client relationships.
NBJ: Given the current economic
situation, how can industry leaders
continue growing the industry and
secure its long-term prospects?
ML: We need to address the concerns
of the consumer in enhancing self care.
With people losing jobs and healthcare
coverage, we need to be proactive in declaring
and demonstrating the virtues of
supporting self care through ingesting
responsibly made dietary supplements.
As data becomes available showing the
benefi ts to society at large from supplements
for target populations, we need to
get that message out not only to the public,
but to the media and the regulatory
community as well. One story we should
be telling is how daily supplementation
of specific nutrients can reduce hip fractures
in the elderly and thereby significant decrease expenditures in the Medicare
system. Enhancing and restoring
confi dence in the use of dietary supplements
is one of our long-term goals. To
the extent that we merge that goal with
the desire to reduce preventable disease
states in at-risk populations through dietary
supplements, I believe we have
a sound recipe for securing long-term
success for the industry.
NBJ: What’s going to be necessary
moving forward that maybe wasn’t
required just a few years ago?
ML: A dedication to actual adherence
to the new regulatory framework associated
with GMPs is key to the long-term
viability of the U.S. supplement industry.
A renewed effort at self regulation—
such as is reflected in CRN’s work with
the National Advertising Division (NAD)
of the Council of Better Business
Bureaus to encourage the industry to
crack down on blatantly false supplement
advertising claims—is also crucial.
Willingness to have frank discussions
with the research community is important,
as well.
NBJ: How would you characterize
the current state of scientific research
coming out of the supplement
industry?
ML: At a recent industry conference,
Dr. Josephine Briggs, director of the National
Center for Complementary& Alternative Medicine (NCCAM),
indicated that she believed the methodology
for evaluating natural products
needs to be revisited. The gold-standard
drug model, in her mind, is fl awed, and
she encouraged alternative approaches
to future inquiries. On that issue, I believe
the historical gold-standard investigational
technique of a double-blind,
placebo-controlled, crossover study is of
limited value in the dietary supplement
industry. That said, we need to collaboratively
find ways to validate efficacy
and eradicate chicanery.
Many participants in the industry have
cut back on investigations for a variety
of reasons, chief among these is probably
associated with a cost-benefit analysis and the potential lack of recovery of
research costs with associated product
sales and the lack of exclusivity afforded
under current business models. In
our early years, we spent considerable
sums on human studies to verify value
for our clients and ourselves, but of late
we have focused more of our resources
on the capital intensive requirements
for process validation, ingredient and
finished-product testing and GMP compliance
both here and abroad. Those
expenses are likely to continue for the
foreseeable future.
NBJ: What’s it like to be one of the
few publicly traded fi rms in the nutrition
industry?
ML: It’s getting lonely. The consolidations
of the past few years have been
amazing. Being public allows interested
investors to participate via proxy
in the industry. Given the fact that the
demographics are very much suited to
promote growth in the industry, the
current thinking is that being a publicly
traded company is probably not such a
bad thing, assuming the equity markets
return to some semblance of normalcy.
Still, the significant costs associated
with being a public entity under the
Sarbanes-Oxley Act of 2002 are quickly
changing the equation in favor of other
potential alternatives, such as going private.
The benefi t of being a public company
is the transparency of the business
and the evidence of a strong balance
sheet in these trying times. Short-term
fluctuations in profits or losses, many
of which are often caused by currency
translations or discontinued operations
costs, are a good way to keep score in
a baseball game, but our long-term goal
remains long-term success. The costs
of being a public entity are significant,
probably in excess of $1.5 million dollars
annually. Hopefully, the current economic
environment will return to some
element of normalcy, allowing real valuations
to shine through in a landscape
littered with demolished balance sheets
and excessive leverage.
NBJ: How do you believe an Obama
administration will impact the dietary
supplement industry?
ML: President Obama will most likely
have his hands full with much more
pressing issues than our industry. However,
his selection of Tom Daschle to be
the secretary of Health and Human Services
is a positive development. Senator
Daschle is a pragmatist and is very much
in favor of sensible regulations favoring
consumer protection, while affording input
from responsible parties with a demonstrated
track record of excellence. We
remain hopeful that as evidence materializes
showing the signifi cant economic
benefits of supplements taken for years
versus expensive procedures to rectify
past defi ciencies, President Obama will
see value in requiring Medicare and
Medicaid to change their roles from being
reactive to more proactive with regard
to healthcare. This change alone
could conceivably save trillions over
several generations.
NBJ: What regulatory threats to
the supplement industry do you see
on the horizon?
ML: The change of leadership in Washington
with Congressman Henry Waxman
taking the chair for Energy and
Commerce is something nobody could
have predicted just three months ago.
While many in the industry are concerned
over this development, I believe
that there are many other issues of
signifi cant import to the health of the
economy [that supercede] any issues
regarding dietary supplements. Furthermore,
with the passage of the AER
[adverse event reporting] legislation and
the implementation of GMPs for dietary
supplements, the areas of signifi cant
concern have been greatly winnowed.
NBJ: What is the supplement manufacturer’s
role in educating physicians
and other health practitioners
on the benefi ts of dietary supplements?
ML: I have often stated that physicians
and pharmacists are thought leaders in
shaping consumer opinion. The recent
study commissioned by CRN’s Life-Supplemented
program demonstrated that
the majority of physicians and health
professionals take supplements. Clearly,
they know something about their intrinsic
value. We have to provide essential
data that is scientifi cally valid to them
in a meaningful and unbiased way to
balance the messages coming from our
detractors. I think the message should
be that supplements are not intended to
replace good eating and lifestyle choices,
but in this day and age, are essential
in making up for real defi ciencies in our
food ingestion habits. We also need to
communicate the role supplements play
in combating environmental insults,
such as stress and chemical pollutants.
Fundamentally, I believe it is the role of
responsible industry in a collective manner
to provide the tools to educate the
physicians and health practitioners of
new developments in our world.
NBJ: Some say the supplement
industry is moving into a mature
phase. Do you agree?
ML: The capacity of the industry seems
to be adequate, but with the advent of
the GMPs this may not remain the case.
New companies engaged in developing
new products for new markets may find
themselves with a smaller number of
suppliers given the signifi cant requirements
for quality under the new federal
regulations. The capital constraints of
the credit crisis also are having a bearing
on barriers to entry, which may constrict
further development. There may
be some pricing power returning in the
next couple of years, but this is currently
being buffered by mitigating disinflationary forces. Supply chains may
experience some reconfigurations as
well, with expanded opportunities and
increased risks.
NBJ: You are widely recognized as
one of the funniest guys in the industry.
What is the funniest thing
you heard in 2008?
ML: I heard a lot of funny stuff, for example:‘The bounce in real estate prices
is just around the corner,’ or ‘Oil is
going to $200 a barrel so it is time to
lock in supply contracts for petroleumbased
materials’ or ‘My 401(k) is now a
101(k).’ OK, so maybe those aren’t so
funny, but they do reflect what we all
faced in 2008. |