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Registration for Public Testimony
Classes to be Reviewed
Alzheimers Agents
Analgesics/Anesthetics, Topical
Androgenic Agents
Antibiotics, Vaginal
Antidepressants, Other
Antidepressants, SSRIs
Antiemetics
Antifungals, Oral
Antifungals, Topical
Antiparasitics, Topical
AntiParkinsons Agents
Antivirals, Oral
Atopic Dermatitis
Bone Resorption Suppression and
Related Agents
Bronchodilators,
Anticholinergics
Bronchodilators, Beta Agonists
Cephalosporins and Related
Agents
Cytokine and CAM Antagonists
Fluoroquinolones, Oral
Glucocorticoids, Inhaled
Hypoglycemics, Incretin Mimetics,/Enhancers
Hypoglycemics, Insulins
Intranasal Rhinitis Agents
Leukotriene Modifiers
Macrolides/Ketolides
NSAIDs
Ophthalmics for Allergic
Conjunctivitis
Ophthalmics, Glaucoma Agents
Pancreatic Enzymes
Platelet Aggregation Inhibitors
Stimulants and Related Agents
New Categories
Antihyperuricemics, oral
Antipsychotics (formerly
Atypical Antipsychotics)
Antivirals, Topical
Opthalmic Antibiotics
(previously Opthalmics, Fluoroquinolones and Macrolides)
Opthalmic Antiinflammatories
(previously Opthalmic NSAIDS)
Tetracyclines, Oral
Single Drug Reviews
Analgesics, Narcotics - Long
Acting (Dilaudid liquid)
Anticonvulsants (Banzel, Vimpat)
Bladder Relaxants (Toviaz)
BPH Agents (Rapaflo)
Hypoglycemics, Meglitinides (Prandimet)
Lipotropics, Other (Trilipix)
Phosphate Binders (Eliphos)
Proton Pump Inhibitors (Kapidex,
Prilosec suspension)
Ulcerative Colitis Agents (Apriso, Sfrowasa)
Public testimony at the August
20, 2009 Pharmacy and Therapeutics Committee meeting will be
limited to fifteen (15) presentations: twelve (12) speakers
from the drug industry and three (3) representing consumer
interests. To the extent that the full allotment for either
group does not pre-register to speak, representatives from the
other group will be selected in their place. In the event
speakers are selected and fail to appear at the meeting, their
time will be forfeited, and that slot will remain unfilled. We
will start calling on speakers at approximately 9:20 a.m. This
part of the meeting will last approximately one and one-half
hours.
Speakers will be called upon to give their presentations
in the order that their
names are drawn in the speaker lottery.
The time available for each presentation is up to five minutes.
Thirty seconds before the end of the presentation, speakers will
receive a warning that time has almost expired.
The deadline for
registering to speak at the August 20, 2009 meeting is August 6,
2009. Only one speaker per company, or organization may
register to speak. In the case of subsidiaries of
conglomerates, one speaker from each subsidiary may register to
speak. Speakers may share their time slots. However, there may
be only one time slot given to a company or subsidiary.
In the event more speakers have
registered than there are spaces available, a lottery will be
held to select 15 companies and consumers at random on the day
after the deadline. A disinterested party in the presence of
witnesses will draw the names. All registrants will be notified
within twenty-four hours of the drawing, whether or not they
have been selected. Winners will be advised of their position
in the order of speakers. To register, potential speakers must
provide their full name, phone number, the therapeutic class(es)
and drug(s) they wish to cover, organization and place of
business to Megan Shook of the Maryland Pharmacy Program.
Submit applications by e-mail, fax, U.S. mail or any recognized
carrier. E-mail submissions are preferred. Potential speakers
for the Thursday, August 20, 2009 P&T Committee meeting may
submit their request using the form at
MarylandPDLQuestions or fax them to 410.333.5398 or
mail them to the Maryland Pharmacy Program, 201 W. Preston
Street, Room 408, Baltimore, Maryland 21201. If you have a
change in your choice of person to speak, please notify Ms.
Shook as soon as possible after the change.
Speakers are asked to provide two
business cards to the registration attendant at the meeting.
Speakers'
handout information should be submitted to the Maryland Pharmacy
Program (MPP) electronically at least two days prior to the
meeting. With permission from MPP staff, handouts may be
submitted on the day of the meeting when signing in.
Bring at least 22 copies of any handout material to the
registration attendant. Pharmacy Program staff will distribute
the handouts to the P&T Committee members and staff prior to
speakers taking the microphone. Handouts are limited to no more
than two standard 8-1/2 by 11 inch pages of “bulleted” points
(or one page front and back) per five-minute time-slot. At the
meeting, speakers are required to state their name, organization
and city of business. Audio-visual equipment will not be
allowed because of the time constraint.
Submission of Written
Material to Committee
Written information from
consumers or drug manufacturing companies who are
of the selected speakers may be submitted to the Pharmacy
and Therapeutics Committee. E-mail communication is preferred;
however, it must be compatible with MS-Word or in Adobe®
Acrobat® format. The Pharmacy Program will forward e-mails
received before August 13 to the members of the Committee.
Charts and graphs may be submitted in MS-Excel® or Adobe®
Acrobat®. Attach your material to an e-mail to:
MarylandPDLQuestions@dhmh.state.md.us. Hard copies
of written information may be mailed or delivered to Megan
Shook, Clinical Pharmacy Services Division, Room 408, Dept. of
Health and Mental Hygiene, 201 W. Preston St., Baltimore, MD
21201. If the information is contained on two pages or less, we
will copy it and send it to the P&T Committee members. If it is
more than 2 pages, please enclose at least 13 copies packaged in
individual envelopes with sufficient US postage attached. The
Pharmacy Program will affix address labels to your envelopes and
forward them to the P&T Committee members. Materials received
with insufficient postage will not be forwarded. Binders and
heavy material must be placed in individual padded envelopes.
To ensure sufficient time for review, the mailed material must
be received at DHMH at least two weeks prior to the meeting.
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