Legal and Regulatory Sites
of Interest to Medical Device Manufacturers
The Agency for Health Care Policy
and Research (AHCPR), a part of the Public Health Service within the U.S.
Department of Health and Human Services, is the lead federal agency charged
with supporting research designed to improve the quality of healthcare, reduce
its cost, and broaden access to essential services. AHCPR sponsors and conducts
research that provides evidence-based information on healthcare outcomes, quality,
cost, use, and access. The information helps healthcare decision makerspatients
and clinicians, health system leaders, and policymakersmake more-informed
decisions and improve the quality of healthcare services.
Centers for Medicare and Medicaid
Services (CMS) provides health insurance for 75 million elderly, disabled,
and low-income Americans through Medicare and Medicaid. As a federal agency
within the Department of Health and Human Services, CMS develops coverage policies,
regulates laboratory testing, and oversees certification of nursing homes and
continuing-care providers.
CenterWatch.
A listing of more than 41,000 combined industry- and government-sponsored clinical
trials.
ClinicalTrials.gov.
A place to search for research studies being conducted by the National Institutes
of Health (NIH), other federal government agencies, and pharmaceutical companies.
The
Code of Federal Regulations. When you need to check FDA regulations, this
site, also from the House of Representatives, allows you to search by title
and section number, word, and topic, among other alternatives.
Device Advice,
a self-help service from CDRH, is perhaps the best source of information for
anyone entering the medical device market. The interactive program takes you
step by step through everything you need to know and do to get your product
on the market.
Dedicated to improving and preserving the quality of the national and global
environment, the Environmental
Protection Agency (EPA) works to ensure that federal environmental laws
are implemented and enforced effectively. Additionally, the EPA takes steps
to ensure that economic development and environmental protection are integrated
in U.S. foreign and domestic policy, and that public and private decisions affecting
energy, transportation, agriculture, industry, international trade, and natural
resources fully integrate considerations of environmental quality.
The Export-Import Bank of the
United States is an independent government agency that helps finance the
overseas sales of U.S. goods and services. The banks mission is to create
jobs through exports. It guarantees workingcapital loans for U.S. exporters
and the repayment of loans by foreign purchasers of U.S. goods and services.
The agency also offers export credit insurance policies to protect against political
and commercial risks of a foreign buyer defaulting on payment.
FDA's Center for Devices
and Radiological Health. The CDRH site is clearly the first stop for regulatory
information. It includes a center overview, recent CDRH federal register notices,
blue book memoranda, and much more. Contact information for each department
and program area is provided on the CDRH
Referral List.
The Food and Drug Administration's
Home Page. The parent site of CDRH offers general agency information and
access to other FDA centers and to the Office of Regulatory Affairs. And if
you need titles and contact information for staff members, you can try searching
the Health and Human Services
directory.
FDA's Electronic
Reading Room contains an index of frequently requested FDA documents (rendered
here to cut down on the number of FOI requests the agency gets). Categories
include compliance policy guides, enforcement reports, inspectors' technical
guides, medical devices reports (MDRs), product approval listings, and warning
letters.
The Federal Trade Commission (FTC)
promotes business competition in the United States and polices anticompetitive
practices. The commission also works to prevent false advertising of consumer
products through the regulation of packaging and labeling, and is the primary
federal agency responsible for enforcing regulations related to on-line fraud
and privacy issues. Its work is divided into the bureaus of Consumer Protection,
Competition, and Economics.
National Institutes of Health
Clinical Center. A searchable listing of research studies being conducted
at the NIH Clinical Center.
The primary goal of the National
Institute of Standards and Technology (NIST) is to promote U.S. economic
growth by working with industry to develop and apply technology, measurements,
and standards. Its major programs are a rigorously competitive Advanced Technology
Program that provides cost-shared grants to industry for development of high-risk
technologies with significant commercial potential; a grassroots Manufacturing
Extension Partnership that helps small and medium-sized companies adopt new
technologies; a strong laboratory effort planned and implemented in cooperation
with industry and focused on measurements, standards, evaluated data, and test
methods; and a highly visible quality outreach program associated with the Malcolm
Baldrige National Quality Award.
NSSN: A National Resource for
Global Standards provides US, foreign, regional, and international standards
and regulatory documents for purchase or free download, when possible. Users
can subscribe to the Standards Tracking and Automated Reporting (STAR) service,
which notifies them via e-mail whenever a particular standard gets updated or
altered.
The U.S. Nuclear Regulatory Commission
regulates the civilian use of by-product materials in the United States to protect
the public health and safety, the environment, and the common defense and security.
The agency reviews and issues licenses for construction and operation of nuclear
power plants and other nuclear facilities, and it licenses the possession and
use of nuclear materials for research and medical, industrial, and educational
purposes.
The Occupational Safety and Health
Administration (OSHA) develops and promulgates occupational safety and health
standards, develops and issues regulations, conducts investigations and inspections
to determine the status of compliance with safety and health standards and regulations,
and issues citations and proposes penalties for noncompliance. OSHA enters into
partnership agreements to promote workplace safety and health, and engages in
training and outreach programs to educate employers and employees.
The Occupational Safety and
Health Review Commission, an independent federal agency, decides contests
of citations or penalties resulting from OSHA inspections of the workplace.
The commission has established procedures for conducting hearings, receiving
evidence, and rendering decisions by its administrative law judges.
A primary responsibility of the U.S.
Department of Commerce Office of Microelectronics, Medical Equipment, and Instrumentation
(OMMI) is to promote exports and increase international competitiveness
of the U.S. medical device industry. The office helps firms promote medical
products in international markets. Programs include working with industry to
develop trade missions, exhibitions, and seminars that promote exports; participating
in and supporting trade negotiations to increase U.S. exports and international
investments abroad; reducing and eliminating regulatory barriers that impede
trade; and preparing industry analysis reports that affect U.S. competitiveness
and future trends. OMMI and the Commercial Service organize a significant number
of medical device trade events each year.
RegSource features
links to regulatory news of interest to medical device manufacturers. A device
industry directory offers information ranging from upcoming conferences and
meetings to standards and GMPs. Links to FDA's Federal Register and Title
21 of the U.S. Code are also available. A searchable database of Federal Register
notices, as well as information on regulatory forms and warning letters, is
provided.
The U.S. Small Business Administration
(SBA) provides new and established small businesses with financial assistance,
management counseling, and training. The administration also licenses and regulates
small business investment companies. Special programs have been developed by
SBA to expand and promote ownership of businesses by women and minorities.
Thomas: U.S. Legislative Information.
This site offers the fully searchable text of House and Senate bills as well
as the full text of the Congressional Record.
The United
States Code. This browseable version of the U.S. Code from the House of
Representatives gopher offers a quick way to find U.S. laws covering the device
industry by title and section numbers (you'll generally want Title 21). If you
need to do a search by keywords, the Cornell University Law School provides
a searchable version.
The U.S.
Patent & Trademark Office Database covers the period from January 1, 1976
to the most recent weekly issue date. The database consists of the full text
of US patents (including utility, design, reissue, plant and SIR patents). The
full text of a patent includes all bibliographic data, such as the inventor's
name, the patent's title, and the assignee's name, as well as the abstract,
the full description of the invention, and the claims.

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