I am looking forward to our annual plenary meeting ISO
Technical Committee 212. This one is at
the MGM Grand in sunny and warm Las Vegas.
A lot of discussion, and maybe some time for a show. ISO meetings are an interesting
experience. They remind me of that there
is no “I” in TEAM” but there is a
big one in “ISO” and a small one in “Quality”.
ISO (aka the International
Organization for Standardization) is a collective of individuals each representing their country, their region, their
organization and themselves. There is a
large wack of egos (including mine) in the room each there addressing a series
of personal agendas. On the highest
level, there is the Prime Directive to ensure that any standard that gets created
meets the needs of each individual
country and region. The whole point of
ISO is to set rules that will create and foster the foundations for common
trade, business alliances and product compatibility. If a document is created with undue unfairness
or bias then a country’s business and trade can be compromised.
I often remember the conversation
that I had with a long-time colleague who told me that his specific instruction
from his country was to attend these particular meetings and ensure that no
document would ever see the light of day unless it was fully compatible with his
country’s specific health system needs.
Individuals are very much
aware that they attend these meetings at the pleasure of their employers. Time to attend and participate in meetings in
nice hotels in nice places comes with certain expectations. For manufacturers they want to see their
products on the winning side. For
accreditation bodies, they need to see opportunities for documents that can be used
to help laboratories in their specific region.
For consultants they need to see opportunities for doing their
consulting thing and making money. And
for academics it is about the books and manuscripts and coursework edge. And for “bloggers” it is a gold mine for
shared opinion and experience.
None of this is bad
stuff. We might as well put our money on
the table and acknowledge our collective vested interests. What happens is course is that all these
interests intermingle as the standards development process moves forward. A little bit of altruism and a large dose of
collective, sometimes incompatible self-interest trying to find that place
where everyone can live with the outcome.
As complicated as it sounds,
what is remarkable that when the smoke clears it usually works fairly well,
baring the unintended consequences that can arise, but more on that another
time.
I will tell you that there
is one collective loser in the process.
Resources limited regions (RLRs) always get ignored or always get the
short end of the stick. Folks from RLRs
rarely have the resources to attend meetings and participate in the
discussion. The interests of the RLRs
get subsumed by the interests of the attenders.
So the documents usually are a collective of wealthy region assumptions
and wealthy region practices. Many of
the requirements are so far outside of the reality of the RLRs that their
opportunity to adopt these documents in a meaningful way is all uphill and near
impossible. Good for the 1 percent, but rarely a successful strategy for the remaining
99. This could be fixed if RLRs were
represented and were in a position to stand up for their reality and
circumstance. But this will
unfortunately take a long time and a massive amount of work to overcome.
An organization like the Gates
Foundation could make dramatic steps forward in RLR health by a judicious use
of representation money and resources with a lot of strings attached. Bill, if by chance you are out there reading this, give me a call J.
But there is another “i” that is important to consider. Documents like ISO 15189 and 9001 and 9004
and even (shutter) 17025 can enhance operational quality for the medical
laboratory. There is an "i" in Quality and It is in every person’s best
interest for quality processes to succeed.
For the employee Quality
programs enhances personal TEEM (time, effort, energy and money). Structure reduces time to the detection of
error and reduces the effort and energy for getting back on track. Reduced error saves the budget, and reduces
the risk of budget overruns thereby protecting positions. In the private sector, Quality increases
profit.
For the patients, quality
reduces error and distrust and frustration, and reduces the need for looking
for compensation (as in reducing the risk of malpractice suits). For the clinicians it speeds up the process
to high value diagnostic information.
None of this is bad, indeed self interest is a motivator to make ones life better, and if it helps others at the same time, that is OK. Gordon Gecko (a
character in the 1980`s movie Wall Street said “Greed is Good”. Well, by the same spirit, self interest in Quality
is also all for the good”.
More on the ISO meeting
coming up.
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