[Federal Register: December 30, 2005 (Volume 70, Number 250)]
[Notices]
[Page 77398]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr30de05-57]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
Public Notice
AGENCY: Centers for Disease Control and Prevention (CDC), Health and
Human Services (HHS).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), National
Center for Infectious Disease (NCID), Division of Bacterial and Mycotic
Diseases (DBMD) and the National Immunization Program, Epidemiology and
Surveillance Division through its component Branches have lead
technical responsibility for research, development and evaluation of
diagnostic tools for pertussis and application of these to
epidemiologic studies of pertussis. CDC uses epidemiologic, laboratory,
clinical, and biostatistical sciences to control and prevent vaccine
preventable infectious diseases. CDC also conducts applied research in
a variety of settings, and translates the findings of this research
into public health practice.
CDC is seeking to evaluate commercial products, or products in
development, for in vitro serological diagnosis of pertussis.
Specifically these should include tests to detect anti-pertussis toxin
antibodies in infected and vaccinated individuals. The tests should be
based on standardized reagents commonly used in the field (such as FDA
Reference Serum Standard Lot 3 or equivalents). Products will
be evaluated in CDC and collaborating laboratories and if appropriate,
may be used in epidemiologic validation studies. Data obtained from
this comparative analysis may be used by CDC in making recommendations
and decisions for diagnosis of pertussis in the public health setting.
Interested organizations that may have candidate products are
invited to submit documentation for CDC to assess whether the offered
product(s) are at a sufficient stage of development to be included in
this comparative analysis. As a minimum, submitted information should
be sufficient for CDC to determine the following for each candidate
product: (a) Product package insert or detailed instructions for use;
(b) Detailed information to determine if the product is calibrated to a
recognized standard; and (c) Preliminary data demonstrating suitability
for validation studies.
Organizations that have products selected by CDC for this
comparative analysis will be required to enter into an appropriate
agreement prior to the transfer of any material to CDC. Sample
agreements may be viewed at the following Web site: http://www.cdc.gov/od/ads/techtran/forms.htm.
All information submitted to CDC will be
kept confidential as allowed by relevant federal law, including the
Freedom of Information Act (5 U.S.C. 552) and the Trade Secrets Act (18
U.S.C. 1905). Only information submitted within thirty days of
publication of this notice will be reviewed to determine if the offered
product(s) will be acceptable for possible inclusion in this
comparative analysis.
Responses are preferred in electronic format and can be e-mailed to
the attention of Michael J. Detmer at MDetmer@cdc.gov. Mailed responses
can be sent to the following address: Michael J. Detmer, Division of
Bacterial and Mycotic Diseases, National Center for Infectious
Diseases, Centers for Disease Control and Prevention, 1600 Clifton Rd.,
NE., Mail Stop C-09, Atlanta, GA 30333.
FOR FURTHER INFORMATION CONTACT: Technical: Dr. Patty Wilkins, Division
of Bacterial and Mycotic Diseases, National Center for Infectious
Diseases, Centers for Disease Control and Prevention (CDC), 1600
Clifton Rd., NE., Mail Stop D-11, Atlanta, GA 30333. Telephone (404)
639-3297, E-Mail at pwilkins@cdc.gov.
Business: Lisa Blake-DiSpigna, Technology Development Coordinator,
National Center for Infectious Diseases, Centers for Disease Control
and Prevention (CDC), 1600 Clifton Rd., NE., Mail Stop A-42, Atlanta,
GA 30333. Telephone (404) 639-2620, E-Mail at LBlake-DiSpigna@cdc.gov.
Dated: December 21, 2005.
James D. Seligman,
Associate Director for Program Services, Centers for Disease Control
and Prevention.
[FR Doc. E5-8103 Filed 12-29-05; 8:45 am]
BILLING CODE 4163-18-P