human-health

Documents about human-health

• 21 CFR Part 290 — Controlled Drugs#506809Code of Federal Regulations (eCFR)
• 21 CFR Part 600 — Biological Products: General#506869Code of Federal Regulations (eCFR)
• 21 CFR Part 822 — Postmarket Surveillance#506895Code of Federal Regulations (eCFR)
• 21 CFR Part 868 — Anesthesiology Devices#506902Code of Federal Regulations (eCFR)
• 21 CFR Part 870 — Cardiovascular Devices#506903Code of Federal Regulations (eCFR)
• 21 CFR Part 872 — Dental Devices#506904Code of Federal Regulations (eCFR)
• 21 CFR Part 882 — Neurological Devices#506909Code of Federal Regulations (eCFR)
• 21 CFR Part 886 — Ophthalmic Devices#506911Code of Federal Regulations (eCFR)
• 21 CFR Part 888 — Orthopedic Devices#506912Code of Federal Regulations (eCFR)
• 21 CFR Part 892 — Radiology Devices#506914Code of Federal Regulations (eCFR)
• 21 CFR Part 895 — Banned Devices#506915Code of Federal Regulations (eCFR)
• 21 CFR Part 1150 — User Fees#506934Code of Federal Regulations (eCFR)
• The experiences and needs of australian medical oncologists in integrating comprehensive genomic profiling into clinical care: A nation-wide survey#190661UNSWorks Repository
• Hydrochemical characterization and integrated assessment of groundwater quality, ecological risk, and human health impacts in Tiruvannamalai district, Tamil Nadu, India under urbanization pressure#268280Figshare
• Replicación de datos para: First reports of envenoming by South American water snakes Helicops angulatus and Hydrops triangularis from Bolivian Amazon: A one-year prospective study of non-front-fanged snakebites.#276409Repositorio de datos de investigación de la Universidad de Chile Dataverse OAI Archive
• Tn5Prime, a Tn5 based 5′ capture method for single cell RNA-seq#492108eScholarship
• Analysis of Trends in Emission of Criteria Air Pollutants and Human Health in an Era of Regulation#499667Munich Personal RePEc Archive
• 21 CFR Part 4 — Regulation of Combination Products#506702Code of Federal Regulations (eCFR)
• 21 CFR Part 10 — Administrative Practices and Procedures#506705Code of Federal Regulations (eCFR)
• 21 CFR Part 11 — Electronic Records; Electronic Signatures#506706Code of Federal Regulations (eCFR)
• 21 CFR Part 12 — Formal Evidentiary Public Hearing#506707Code of Federal Regulations (eCFR)
• 21 CFR Part 17 — Civil Money Penalties Hearings#506712Code of Federal Regulations (eCFR)
• 21 CFR Part 202 — Prescription Drug Advertising#506792Code of Federal Regulations (eCFR)
• 21 CFR Part 203 — Prescription Drug Marketing#506793Code of Federal Regulations (eCFR)
• 21 CFR Part 610 — General Biological Products Standards#506873Code of Federal Regulations (eCFR)
• 21 CFR Part 740 — Cosmetic Product Warning Statements#506882Code of Federal Regulations (eCFR)
• 21 CFR Part 803 — Medical Device Reporting#506885Code of Federal Regulations (eCFR)
• 21 CFR Part 812 — Investigational Device Exemptions#506891Code of Federal Regulations (eCFR)
• 21 CFR Part 830 — Unique Device Identification#506896Code of Federal Regulations (eCFR)
• 21 CFR Part 876 — Gastroenterology-Urology Devices#506906Code of Federal Regulations (eCFR)
• 21 CFR Part 890 — Physical Medicine Devices#506913Code of Federal Regulations (eCFR)
• 21 CFR Part 900 — Mammography#506917Code of Federal Regulations (eCFR)
• 42 CFR Part 413 — Principles of Reasonable Cost Reimbursement; Payment for End-Stage Renal Disease Services; Prospectively Determined Payment Rates for Skilled Nursing Facilities; Payment for Acute Kidney Injury Dialysis#509960Code of Federal Regulations (eCFR)
• 21 CFR Part 2 — General Administrative Rulings and Decisions#506700Code of Federal Regulations (eCFR)
• 21 CFR Part 15 — Public Hearing Before the Commissioner#506710Code of Federal Regulations (eCFR)
• 21 CFR Part 54 — Financial Disclosure by Clinical Investigators#506718Code of Federal Regulations (eCFR)
• 21 CFR Part 251 — Section 804 Importation Program#506808Code of Federal Regulations (eCFR)
• 21 CFR Part 680 — Additional Standards for Miscellaneous Products#506877Code of Federal Regulations (eCFR)
• 21 CFR Part 810 — Medical Device Recall Authority#506890Code of Federal Regulations (eCFR)
• 21 CFR Part 820 — Quality Management System Regulation#506893Code of Federal Regulations (eCFR)
• 21 CFR Part 821 — Medical Device Tracking Requirements#506894Code of Federal Regulations (eCFR)
• 21 CFR Part 860 — Medical Device Classification Procedures#506897Code of Federal Regulations (eCFR)
• 21 CFR Part 864 — Hematology and Pathology Devices#506900Code of Federal Regulations (eCFR)
• 21 CFR Part 866 — Immunology and Microbiology Devices#506901Code of Federal Regulations (eCFR)
• 21 CFR Part 884 — Obstetrical and Gynecological Devices#506910Code of Federal Regulations (eCFR)
• 21 CFR Part 1114 — Premarket Tobacco Product Applications#506930Code of Federal Regulations (eCFR)
• 21 CFR Part 1143 — Minimum Required Warning Statements#506933Code of Federal Regulations (eCFR)
• A dynamic mode of mitotic bookmarking by transcription factors#491840eScholarship
• 2 CFR Part 300 — Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards#503861Code of Federal Regulations (eCFR)
• 21 CFR Part 500 — General#506843Code of Federal Regulations (eCFR)