Planners in the medical and pharmaceutical fields have faced their fair share of challenges in the past few years. As the meetings industry continues its economic recovery, what are the major concerns still facing these specialists? M&C spoke with a number of leading voices in this niche market to get their views. Here's what med/pharma planners are up against.
1. Keeping abreast of the rules. One of the greatest ongoing challenges for planners of medical and pharmaceutical meetings is fully understanding the influence of regulatory codes, restrictions and legislation, notes Pat Schaumann, CMP, CSEP, DMCP, president of St. Louis-based Meeting I.Q. and U.S. director of its affiliate, China Connect. "It's just mounds of information, and trying to decipher the codes, and to understand the ramifications of the Sunshine Act and health-care reform, is a serious challenge," says Schaumann, who also is founder of the International Medical Meeting Professionals Association.
Self-regulatory industry codes of ethics, as well as both federal and state legislation, deal primarily with interactions with health-care professionals -- and how to avoid undue influence, or the perception thereof, over the prescription and medical-device decisions doctors make. The PhRMA Code on Interactions with Healthcare Professionals, specifically for the pharmaceutical industry, was updated in January 2009, while the latest iteration of the AdvaMed Code of Ethics on Interactions with Health Care Professionals (advamed.org/MemberPortal/About/code), for medical-device manufacturers, took effect the following July.
Both codes offer guidelines for companies within the respective industries; it's up to the companies to develop and enforce internal policies. As such, in an effort to ensure compliance -- or to avoid the public perception that undue spending or influence is occurring -- company policies could change more often than the codes themselves.
Last year's passage of U.S. federal health-care legislation, which included provisions of the long-debated Physician Payments Sunshine Act, requires companies to disclose payments made to health-care professionals -- essentially giving the codes more teeth, as well as adding federal government oversight to the equation. Adding to that complexity is legislation passed in many states over the past several years, much of which specifies payment limits.
In other words, if the code changes caused planners' heads to spin, government oversight should intimidate them into thinking straight. "What's become very clear to companies over the past year," says Schaumann, "is that audits can take place, and you have to be able to account for every penny."
Bringing international health-care professionals to an event further complicates matters, since pharma and ethical guidelines also vary by country.
"The last event we handled was for physicians from 10 different countries," says pharmaceutical-industry planner Christine Kelly, managing director of Cheshire, U.K.-based Gemini International. "And each country had different regulations in terms of the level of hospitality allowed, so we had to find a balance that was suitable for everyone. Particularly in the U.K., that's becoming more and more of an issue." Regulations are different even among countries within the European Union, Kelly adds.
While the pharmaceutical and device companies ultimately bear the responsibility of compliance, notes Schaumann, it is incumbent upon third-party planners, such as her company, to understand the requirements and aid in the process. "If you're planning a health-care meeting or working with health-care companies, you need to stay in the game," she insists. "There's too much on the table, and I think it's up to planners to stay on top of trends and changes." That's a big reason Schaumann founded IMMPA last year. "We're trying to help as much as we can to educate planners about the latest that's happening in the industry," she says.
Of course, understanding the regulations is only part of the challenge. The end result of all the legislation and industry regulation is that companies are being held accountable for their spending, and tracking those dollars is crucial. "On top of needing to keep up with the regulations and what you can and can't do," says Teresa Bria, SMMC, president of Oakland, Calif.-based Bria Events, "there's just the sheer volume, the sheer workload, that's being added to the responsibilities of the meeting planner. My staff probably spends two-thirds of their time dealing with paperwork, and one-third actually planning the meeting."
Top 20 Cities for Med/Pharma Meetings (2009)
1. San Diego
2. Orlando
3. San Francisco
4. Chicago
5. Washington, D. C.
6. Las Vegas
7. New Orleans
8. Boston
9. Phoenix
10. San Antonio
11. Baltimore
12. Seattle
13. Atlanta and Dallas/Fort Worth (tie)
15. Philadelphia
16. Denver
17. New York City
18. Scottsdale, Ariz., and Miami (tie)
20. Tampa, Fla.
Source: Healthcare Convention and Exhibition Association
2. Getting busy people to attend. If
the biggest challenge is understanding and complying with codes and
regulations, explains Joe Lipman, CEO of Summit Management in Cedar
Grove, N.J., a close second is calculating the time constraints of the
health-care professionals you hope will attend. "Travel time,
connections and downtime are all major considerations," says Lipman.
"It's time in which that physician, who can earn as much as $4,000 a
day, is out of the office."
Knowing where your expected attendees
are traveling from is of paramount importance, Lipman explains. Can the
attendees fly direct, or are there connections? How far is the meeting
site from the airport? If you're expecting international attendees, can
they fly directly to the host city?
"If you're bringing in 25
doctors from abroad," says Lipman, "and they have to clear customs in
the arrival city, reboard, and take even a one-hour connecting flight,
that can add about four hours onto the trip, each way. In total, that's
an eight-hour day, no matter how you slice it. That's a solid argument
for moving the meeting to the city with better international flight
service."
You have to consider, too, in which direction most
attendees will be flying, and at what times the majority of those
flights will depart. "Just by shifting the start time and end time of a
two-day meeting," says Lipman, "you can save overnight hotel costs."
It
isn't just the doctors' time that is of concern; if the meeting host is
covering travel, every penny spent is a physician payment that must be
disclosed and counted toward limits. "How much you spend on transfers,
breakfast, lunch and dinner, and the hotel room rate -- everything must
be compliant," Lipman underscores.
Because of all of the
restrictions, it is harder for industry suppliers to get face-to-face
meetings with physicians in general, adds Fred Criniti, who serves as
chief marketing officer for industry education provider Medical
Exchange, based in Weston, Mass. For that reason, he says, we should
expect to see new models emerging at medical conferences that make the
most of such opportunities and increase the efficiency of one-on-one
meetings.
At Medical Exchange's new CollaborativeCARE Conference
(C3), set to debut this November in Long Beach, Calif., organizers will
gather information from exhibitors and attendees to arrange meetings in
advance, by using an automated platform that will match physicians and
product reps based on interests and needs. "It's like a speed-dating
software package," describes Criniti.
3. The growing role of procurement. The
event industry overall has become gradually more procurement-driven in
recent years -- and particularly so in the pharmaceutical sector, notes
Gemini International's Christine Kelly. Working with procurement can
pose a number of challenges to planners, depending on their positions
within a company -- or relationships to their clients, if they are
third-party planners.
"My situation has been affected quite
dramatically, both positively and negatively, by procurement," says
Kelly, whose planning company must participate in procurement bidding
and scoring processes to win business from major pharmaceutical clients.
"For a company of our size, even though we have the experience of
working with world-class clients on a world-class level, in some cases
now it's very difficult to compete with very large agencies that have
the physical size and resources and physical presence in many
countries."
Kelly worked on the client side for many years for a
major pharmaceutical company, and has an additional 20 years of
experience specializing in pharma events with her agency, but she says
that this kind of background sometimes isn't enough to counteract the
weighted scoring that procurement analyses might give to larger, more
global companies, particularly when consolidation of vendors is a
primary motive.
"We've been through a lot of procurement
processes," Kelly notes, "and with some we've been successful, and with
some others we've spent an awful lot of time to find that we've come in a
close second for the job." Such an investment of time and resources
leads many smaller, specialized planning companies to consider some
difficult questions. "We're all having to decide whether or not it's
actually economically viable to actually go through those processes,"
admits Kelly, "or to focus on smaller, niche projects that are more
service-oriented."
Adding to the difficulty is that participating
in such a bid doesn't always guarantee work; sometimes it only earns
the planning company a place on a roster of preferred vendors.
Kelly
believes that procurement's motives of increasing volume and lowering
margins too often commodifies the high level of service offered by
planners. "Companies say they're looking for quality and added value,
and I'm sure they are, but I think that they may risk losing some of
that when they're trying to cut costs and to consolidate," she says.
"I'm not convinced that it's the right way forward with event management
-- to just use one agency to do everything. I think having a range of
specialist providers, and some degree of competition, is a good thing."
In-house
planners face similar issues stemming from procurement's involvement.
It can be both a major challenge and excellent opportunity to convince
procurement -- and executives and marketers, for that matter -- to
leverage planners' expertise and allow them a hand in more strategic
meetings development. In some cases, says Pat Schaumann, planners have
been put in the position of having to educate their procurement
departments about the industry codes and policies. "That's a whole new
element for planners," she says, "and to make procurement understand
can be a challenge." (For advice, see "A Procurement Primer for Meeting
Managers," online at mcmag.com/webexclusives.aspx.)
Verifying CME Attendance
When offering live events for continuing medical education
credit, organizations need to be able to keep track of who's in the room
and whether they complete the session's requirements.
Low-tech solution. The
Center for Continuing Education at Ohio's Cleveland Clinic offers about
1,200 unique CME activities each year, reaching about 190,000 medical
professionals. At the live events, the doctors need to have checked in
and attended to qualify for a course's credit. Not just anyone can
stroll in, though, says Steven Kawczak, associate director of the
Center. Participants are vetted through the preregistration process to
make sure they're right for the course.
Watchful eyes. The
Massachusetts Medical Society–New England Journal of Medicine in
Waltham, Mass., sponsors about 30 live events each year. They add a
policing element to the check-in process to keep track of participants.
"We have CME 'police,' " says Caroline Carregal, MMS director of
continuing medical education. "They observe people going in and out of
the conferences." The hall monitors keep track of who is walking out the
door and not coming back.
High-tech solution. CME
providers who want proof that attendees stayed in the room can use
audience-response technology, like the devices available from
Youngstown, Ohio-based Turning Technologies. Nadine Punke, manager of
conferences and CME for Wisconsin's Marshfield Clinic, uses the data
collected from the keypads to validate learning for CME certifications.
How? The devices can be assigned to individuals, so when they answer
pre- and post-session questionnaires, their responses confirm that they
were in the room and that the required learning took place.
By Sarah J.F. Braley
4. Ever-tightening budgets.
Many planners still are seeing budget cuts, whether they are related to
physician-spend regulations, the still smarting economy or an
unfortunate combination of the two. "That's our biggest challenge," says
Teresa Bria, "continuing to stay within food-and-beverage and
hotel-spend guidelines, when every year the cost of goods is going up."
The amount her clients can spend, however, continues to decrease,
creating the need for more intense negotiations with her vendors.
"When
does it start to affect the quality of the program?" Bria asks. "I
think the pendulum has swung too far. The limits are now starting to
impact quality."
Vendors, too, are feeling the pinch. Omar
Mejias, director of business development for communication-services
provider EarthColor Pharmaceutical, a Parsippany, N.J., marketing firm
serving the pharmaceutical and biotech industries, sees the trend
continuing through the coming year. "It's going to present meeting
planners with a very significant hurdle in some cases," he says.
"Location, premiums, dinner events -- even the pre-meeting packets and
registration processes are impacted as a direct result of the
cost-cutting."
One increasingly common solution, notes Mejias, is
to substitute a smaller, multi-site meeting approach for larger events.
"This is an excellent way to cut the overall cost," he acknowledges,
"but it can bring in much larger issues around the logistics of the
meeting, from multiple registration processes to getting the printed
materials in the proper quantities to the different locations when
needed."
5. Using social media wisely.
The growing use of social media presents a challenge newer than the
others -- and one that still isn't really being addressed. This concerns
IMMPA founder Pat Schaumann. "We're learning about the advantages, of
course, of expanding the learning network through social media, and
we're all using it," she explains. "We're using it for communication and
marketing. But without any internal social media policy, there could be
a real potential for information and privacy risks."
It's a
concern that should be considered by all event managers, of course, but
the ramifications of social media misuse could be particularly
significant in the med/pharma world. "We're a regulated industry," notes
Schaumann, "which means there are people watching; there is
accountability to consider."
Legally speaking, there is little
precedent for social media use gone wrong at events. "The whole thing is
a wide-open area and really something that we have to watch," says
Jonathan Howe, Esq., M&C legal expert and founding partner of
Chicago-based Howe and Hutton Ltd. With respect to publicizing
sensitive information, says Howe, there are some accepted rules in
place: "If people are disclosing secrets at meetings, they might be in
violation of their employment agreements. There's also the issue of
industrial espionage if someone is doing this illicitly."
And
then there's the matter of intellectual property. Copyright
infringement, notes Howe, might be difficult to prove from a
140-character tweet; on the other hand, using copyrighted material
without permission in blog posts has become an area of growing concern.
Some
planners have amped up their efforts to minimize such infringement.
"We've always cautioned about putting a disclaimer on the opening slides
of a presentation to protect your intellectual property," says
Schaumann. But with the speed with which information can be dispersed
from a show, she doesn't think that's enough anymore. "People could come
into a conference late and miss that first slide. Now we're telling
speakers to put it at the bottom of every single slide and every single
handout. They don't have to talk about it, but put it up there, just to
protect everything."
Beyond the meeting planning realm,
companies should be cautioning their employees on what information
should or shouldn't be posted, adds Schaumann. "At every conference
today, it seems, there's a seminar about how to use social media, about
the benefits, the positive side of it. No one is really paying attention
to the negative side. I don't know that companies are addressing this
in their policies and compliances internally. I can tell you I'm not
seeing it in any risk-management plans in working with clients."
6. The perception factor. It's
an issue most planners have battled during the past few years, but
public perception is a particularly potent problem for medical and
pharmaceutical meeting planners.
"Perception of the meeting is
very important," says Joe Lipman of Summit Management Services. "Where
doctors can or cannot go, and where they can or cannot stay, is
constrained by compliance," he notes, but such choices are driven just
as much by public perception as they are by strict adherence to the
specifics of a code.
Lipman rattles off a laundry list of
medical meeting requirements: a property shouldn't have the words beach,
resort, golf or spa in the name; a coastal city may be fine, but a
beachfront property is not; islands with good weather and towns known
for skiing are out; the hotel should be four-star (not five) and,
depending on the city, preferably close to the airport. He names a
handful of popular convention cities that have built-in obstacles,
merely based on location or reputation.
Which isn't to say
medical and pharmaceutical meetings don't happen in these locations, but
it behooves a planner to know how to handle the situation. What if the
site does border the beach, for instance? "You have to be sensitive and
professional about presenting it," Lipman explains. "Our job, when we're
hired, is to try to help the individual who might not know this. That
person might be thinking 'Gee, we want the doctors to come to a place
they're going to enjoy.' We have to bring them a great program, at the
correct amount of money, and stay at the correct type of hotel, without
drawing attention to the fact that it's a medical meeting being held in
that location."
The issue of perception is of particular concern
to pharmaceutical companies, which seem to face an uphill battle in
maintaining a favorable public image. Incentive trips pose a unique
challenge. "Companies continue to organize events to incentivize their
staff," notes Christine Kelly. "But now they give something back as
well."
Kelly knows of one pharmaceutical company, involved in
the area of HIV and AIDS, that rewarded its highest achievers by taking
them to South Africa. After an adventurous few days of touring,
participants spent the last half of their trip volunteering in an HIV
clinic. "So they were actually seeing how their drugs were used and
giving something back, and having a meaningful trip, rather than just
having a lighthearted incentive or reward," Kelly says.
Gemini
planned a similar trip to South Africa for a client that raises funds
for a U.K. charity, in which a few days of white-water rafting and
trekking were followed by volunteering in an orphanage. Participants
worked with the children and staff to renovate a dormitory. In both of
the above cases, says Kelly, participants found the latter parts of the
trips to be the most memorable "because it was so meaningful and,
sometimes, life-changing for them."