Chemical & Biomolecular Engineering

National Institute of Standards and Technology web site of evaluated data on ceramics and superconducting materials. Includes the NIST Superconducting Materials Database, the NIST Structural Ceramics Database, and a collection of Property Data Summaries.

Data on 1000’s of organic and inorganic compounds and reactions, including thermochemical and thermochemical data, IR, mass, UV, visible, electronic, vibrational spectra, physical constants. Search by name, formula, CAS registry number, molecular weight

1996-present. Site includes the full-text and bibliographic records of DOE-sponsored report literature produced by DOE and contractor R&D community.

Department of Energy’s gateway to preprints in scientific and technical disciplines of concern to DOE including physics, materials, and chemistry, biology, environmental sciences and nuclear medicine.

A portal to several databases from the Department of Energy’s Office of Scientific and Technical Information.

Gateway with search engine for finding high quality information resources in Engineering.

Data about the supply, consumption, distribution, and price of energy in the United States. Includes petroleum, natural gas, coal, nuclear, electricity, and various forms of renewable energy.

Mineral Commodity Surveys, Industry Surveys, and Minerals Yearbook from the US Geological Survey.

Technical Publications from the National Institute of Standards and Technology - includes searchable index of forthcoming, recent and past publications from NIST, links to lab collections and bibliographies and full-text of NIST’s Journal of Research.

Government web site with news, grants, and links relating to nanotechnology research.

Provides outputs of scientific & engineering research in different categories.

National Institute of Standards and Technology is a U.S. Commerce Department agency offering standards in several scientific areas. Many are available in html format on their web site.

Major portal of scientific information from the US Government research laboratories, departments and agencies.

Business, economic and trade data from the U.S. Department of Commerce. Includes National Trade Data Bank (NTDB) and its foreign market research reports.

Science Library (SL) Ref, HA 154 .S69 1997

Statistical lets you find all statistics issued by the U.S. government back to 1973, some 1,000 of the best statistical publications of private and state government sources from 1980 forward

Valuable source of information on toxic substances currently in use. Used by government and industry to notify the public and to aid in protecting the environment. TRI published by USEPA.

WorldWideScience.gov is a scientific literature aggregator database/site covering databases and journals from the US and 43 other countries

Data USA is a comprehensive website and visualization engine of public US Government data and includes Viz Builder, and data about most sectors, industries, business, population/census, education, social indicators with allowances for maps and visualizations.

this agency is responsible for the regulatory passage of pharmaceuticals and medical devices.

Chapter 21 - Food and Drugs
Chapter 42 - Public Health
This is the official compilation of federal regulations.
Full print: LL REF KF 70 A3

GAO, 2009

The table contained in this link lists all official FDA Guidance Documents and other regulatory guidance. You can search for documents using key words, and you can narrow or filter your results by product, date issued, FDA organizational unit, type of document, subject, draft or final status, and comment period.

This feature is provided to give a convenient way to search for all FDA guidance documents from a single location.

If you cannot find the document you’re looking for here, you can browse separate collections of guidance documents by topic.

Review of Regulatory Basics that includes videos on different aspects including Regulatory Pathways, Guidance for Mobile Medical Applications, and Regulatory Expertise.

Searches across multiple FDA Databases, including the device listing database,510(k) and PMA databases. Recommended for device classification coverage.

Lists the medical specialties used to review medical devices.

Enables users to classify a device based on the device name, review panel, regulation number, producy code, submission type, third-party eligibility and device class.

Database contains mechanical, physical & biological responses as well as drug compatibility properties for the materials & coatings used in medical devices for cardiology/thoracic, orthopedics, neurological, and general surgery plus some coverage for urological, dental & anesthesiology. Includes FDA Emergency Use Authorized Devices ( including FDA EUA directives for latest COVID-related devices; Emergency Guidance Documents from FDA: EUAs, UK Medicines & Healthcare products Regulatory Agency, Australia's Therapeutic Goods Administration & Health Canada; latest FDA Approved devices (510(k) and PMA with links to associated materials, coatings & drugs noting producers, recalls and guidance documents.

covers strategies for surgical gowns and masks, medical glove conservation, and ventilator supply mitigation

Reviews 4-step review process for pre-market approval.

Premarket approval (PMA) is the FDA process of scientific and regulatory review to evaluate the safety and effectiveness of Class III medical devices. Class III devices are those that support or sustain human life, are of substantial importance in preventing impairment of human health, or which present a potential, unreasonable risk of illness or injury.

An approved Premarket Approval Application (PMA) is, in effect, a private license granted to the applicant for marketing a particular medical device.

A 510(K) is a premarket submission made to FDA to demonstrate that the device to be marketed is as safe and effective, that is, substantially equivalent, to a legally marketed device (section 513(i)(1)(A) FD&C Act) that is not subject to premarket approval.

The MAUDE database houses medical device reports submitted to the FDA by mandatory reporters 1 (manufacturers, importers and device user facilities) and voluntary reporters such as health care professionals, patients and consumers.

This database includes:

medical device manufacturers registered with FDA and
medical devices listed with FDA

Note: Registration of a device establishment, assignment of a registration number, or listing of a medical device does not in any way denote approval of the establishment or its products by FDA.

Database contains mechanical, physical & biological responses as well as drug compatibility properties for the materials & coatings used in medical devices for cardiology/thoracic, orthopedics, neurological, and general surgery plus some coverage for urological, dental & anesthesiology. Includes FDA Emergency Use Authorized Devices ( including FDA EUA directives for latest COVID-related devices; Emergency Guidance Documents from FDA: EUAs, UK Medicines & Healthcare products Regulatory Agency, Australia's Therapeutic Goods Administration & Health Canada; latest FDA Approved devices (510(k) and PMA with links to associated materials, coatings & drugs noting producers, recalls and guidance documents.