| R. Lewis Dark:
Heparin, China, Reagents, and Your Lab
MANY OF YOU HAVE HEARD THE NEWS about the contaminant that was found
in the heparin manufactured and sold by Baxter International, Inc.
Authorities, responding last fall to reports of hundreds of bad reactions and
19 deaths to the drug, quickly focused on the Chinese companies that supplied
the ingredients used by Baxter to manufacture heparin.
In recent days, the FDA announced that the contaminant was over-sulfated
chondroitin sulfate. Chondroitin sulfate is "abundant and cheap," according to an FDA official quoted in The Wall Street Journal. Chondroitin
is frequently sourced from animal cartilage and, when sulfate is added, the
compound clumps together with heparin in a fashion that makes the contaminant
challenging to identify in regular quality control testing.
Further, authorities now say that the contaminate was added early in the
supply chain in China. Thus, it was already in the raw heparin that Scientific
Protein Laboratories (SPL) purchased in China which it then processed
into the active pharmaceutical ingredient that SPL sold to Baxter.
This latest episode of flawed or dangerous Chinese productsmaking theirway
to the United States reminds us that manufacturing in many countries across the
globe lacks the rigorous oversight and quality control standards that we take for
granted in the United States and Europe. It also leads to this question: How many
in vitro diagnostics (IVD) manufacturers and vendors are sourcing reagents,
chemicals, and similar compounds fromcompanies in China? Is there a risk that
poor quality reagents or other flawed products that American IVD suppliers
could be purchasing in China might move undetected through distribution
channels, eventually reaching clinical laboratories in this country?
This is a reasonable question for labs to ask their IVD suppliers. After all,
just in the past year, we have seen pets die from contaminated pet food and
the discovery of tainted toothpaste, seafood, vitamins, and food additives. The
contamination of heparin, a prescription drug, is just the latest example. To
my knowledge, no major IVD manufacturer has issued a press release declaring
its status relative to its purchase in China of reagents, chemicals, and other
compounds used in its products. That disclosure might be a smart, proactive
business strategy by leading IVD manufacturers. Their laboratory customers
deserve the right to know if,what, and howmuch of the products they buy and
use contain components made in China.
Bostwick Labs Prepares For Public Stock Offering
Noted uropathologist David G. Bostwick, M.D.
is pathology’s newest successful entrepreneur
CEO SUMMARY: In recent years, annual revenue at
Bostwick Laboratories has skyrocketed, reaching $102.8 million
in 2007. Now the company, known for its national
uropathology expertise, has filed documents in preparation for
an initial public stock offering (IPO). Bostwick Laboratories is
the latest success story in anatomic pathology. It hopes to
raise $100 million and is preparing to expand its diagnostic
services into other anatomic pathology subspecialties.
Hospital Lab Takes CMS To Court in CLIA Case
California Hospital takes CMS to federal court
to fight revocation of its lab's CLIA certification
CEO SUMMARY: A California hospital challenged CMS in
federal court over the threatened loss of its lab’s CLIA certificate.
CMS threatened to revoke the certificate in 2007 and stop
paying the hospital's Medicare and Medi-Cal lab bills. In
January, Victor Valley Community Hospital won a court injunction
preventing CMS from revoking its CLIA certificate. Now the
case is undergoing federal administrative review and CMS continues
to press its case for revoking the lab’s CLIA certification.
Labs Should Prepare for Tighter CLIA Enforcement
CMS is stripping labs of their CLIA licenses
for inadvertent violations of PT procedures
CEO SUMMARY: Lab directors and pathologists should take
notice of disturbing newdevelopments in enforcement of CLIA regulations.
During the past year, CMS officials have revoked the CLIA
certification of several hospital laboratories for what are, essentially,
inadvertent violations of proficiency testing (PT) procedures.
Revocation of lab's CLIA certification lasts for one year, and also
includes a sanction that prevents the lab director and the lab
owner from operating or owning a laboratory for two years.
Ascendium Consulting Is New Firm In Lab Market
Demand by labs for strategic and operational
consulting services encourages new company
CEO SUMMARY: Growing numbers of laboratories are taking
steps to reengineer work flow, evaluate automation solutions,
and improve the operational performance of their
laboratory. This is fueling a demand for laboratory consulting
services and Ascendium Consulting is this newest healthcare
and lab consulting company in this marketplace. It became
operational on January 1, 2008, as a result of Roche Diagnostics,
Inc.’s decision to divest its Healthcare Solutions business unit.
Legal Update: Medicare Competitive Bid Lawsuit
Heads toward a Judge’s Ruling
Digitization of Pathology Is Making Steady Progress
New technology and innovations contribute
more capabilities to digitized pathology systems
CEO SUMMARY: Pathology digitization incorporates a greater
scope of work-changing technologies than telepathology. It incorporates
information technology, new diagnostic knowledge, and
other engineering innovations to help pathologists move past
glass and paper. Existing digital pathology systems are already
helping pathologists reduce their travel from site to site by
enabling them to view digitized images from a central location.
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