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Held just weeks before the momentous August 8 deeming regulation deadline, the 84th annual

IPCPR show was a forum for information

sharing and new product debuts.

By Jennifer Gelfand

Highlights From

ICPCR 2016

L

ike many newly regulated tobac-

co product categories, the cigar

industry has been buzzing with

activity in the months since FDA’s May

10 release of the final deeming regula-

tions. Not surprisingly, July’s Interna-

tional Premium Cigar & Pipe Retailers

Association show became the place to be

as retailers, manufacturers and virtually

anyone having anything to do with cigars

sought to get out in front of the regula-

tory wave coming their way.

Manufacturers in particular were

scrambling to get products already in

the pipeline onto the market by August

8, 2016, the deadline by which a product

had to be out before being subject to pre-

market approval in order to be placed on

store shelves at all. But retailers were

equally overwhelmed as they tried to

make sense of a murky ruling that sug-

gested many of them would possibly be

considered manufacturers under the new

regulatory scheme, and to understand

what would and would not be allowed in

terms of sampling and displaying prod-

ucts. By the time July’s show opened,

virtually everyone in the industry was

desperate for information—information

that doesn’t really exist yet, cautioned

Barry Schaevitz of Fox Rothschild.

“We are at the very, very beginning

of a very long process,” he told an audi-

ence of IPCPR attendees and exhibitors

who turned out in droves for industry

sessions held the day prior to the trade

show floor opening. “There is at least as

much that we don’t know about how this

will work as that we do know…we need

to have patience. I know it’s hard, but a

lot will change.”

One of the biggest potential changes—

a changing of the predicate date—is one

that the industry would welcome. Cur-

rently, the predicate date is February 15,

2007, which means any product on the

market by that date will not be required

to go through FDA’s pre-market approval

process at all as long as no changes are

made to the product. Any product that

went on the market after that date but

EVENT HIGHLIGHT

72

TOBACCO BUSINESS INTERNATIONAL

SEPTEMBER/OCTOBER 2016