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CRA’S CIGAR CORNER

BY J. GLYNN LOOPE

T

he year is 2020. The trauma of

the first measure in the history

of America to regulate premium

handmade cigars by the federal govern-

ment has taken hold. The aftermath of

that morning, May 5, 2016, while almost

being a distant memory, is now being re-

membered as the most dramatic turning

point in the history of this artisan in-

dustry. The ramifications of it, however,

are still being viewed with shock by the

surviving manufacturers and retail tobac-

conists, and a legion of consumers with

their own share of concerns.

While the fall season of 2016 quickly

arrived and the initial set of cigar regu-

lations began, the industry anxiously

awaited the outcome of the election sea-

son, hoping that it would spark a change

in management at the U.S. Food and

Drug Administration (FDA), responsi-

ble for that initial listing of 499 pages of

regulations. Companies began to register

with the government, noting their con-

tact information and a list of the cigars

they produced.The initial rule that called

for a ban on samples began, sparking an

uncomfortable feeling when cigars were

exchanged between friends, company

representatives and retail tobacconists.

Were they breaking the law? Or were

they simply harkening back to the days

when exchanging cigars was a simple act

of friendship, or just an effort to discover

a new blend or favorite new cigar? No

one knew. It was a new form of social en-

gineering by the government.

But then the real impact started to

settle in. Companies had to begin sub-

mitting applications for new cigars or

working every conceivable angle to get a

substantial equivalence (SE) exemption

or path to market. The estimated 5,000

hours some said it would take to com-

plete the application process proved to be

true. Lawyers and consultants were rush-

ing in to snatch up clients, with promises

of approval if you used their services—

for a hefty fee.

However, the vision of a federal bu-

reaucracy unprepared for the onslaught

of requests proved true as well. While

the FDA was still behind by thousands

of applications for cigarettes and smoke-

less products, the initial round of more

than 10,000 cigar applications swamped

the agency and created a backlog that

would, according to one projection, last

for three to five years.

The mandate that laboratory test-

ing be conducted for new and existing

blends also created a slowdown, even for

the wealthiest and most sophisticated of

companies. In some cases, the technol-

“Once Upon aTime…”

Cigars in the future will be determined by what we do today.

86

TOBACCO BUSINESS INTERNATIONAL

SEPTEMBER/OCTOBER 2016