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- 42 CFR 8.1 · Scope.
- 42 CFR 8.2 · §thnsp;8.2 Definitions.
- 42 CFR 8.3 · Application for approval as an Accreditation Body.
- 42 CFR 8.4 · Accreditation Body responsibilities.
- 42 CFR 8.5 · Periodic evaluation of Accreditation Bodies.
- 42 CFR 8.6 · Withdrawal of approval of Accreditation Bodies.
- 42 CFR 8.11 · Opioid Treatment Program certification.
- 42 CFR 8.12 · Federal Opioid Use Disorder treatment standards.
- 42 CFR 8.13 · Revocation of accreditation and Accreditation Body approval.
- 42 CFR 8.14 · Suspension or revocation of certification.
- 42 CFR 8.15 · Forms.
- 42 CFR 8.21 · Applicability.
- 42 CFR 8.22 · Definitions.
- 42 CFR 8.23 · Limitation on issues subject to review.
- 42 CFR 8.24 · Specifying who represents the parties.
- 42 CFR 8.25 · Informal review and the reviewing official's response.
- 42 CFR 8.26 · Preparation of the review file and written arguments.
- 42 CFR 8.27 · Opportunity for oral presentation.
- 42 CFR 8.28 · Expedited procedures for review of immediate suspension.
- 42 CFR 8.29 · Ex parte communications.
- 42 CFR 8.30 · Transmission of written communications by reviewing official and calculation of deadlines.
- 42 CFR 8.31 · Authority and responsibilities of the reviewing official.
- 42 CFR 8.32 · Administrative record.
- 42 CFR 8.33 · Written decision.
- 42 CFR 8.34 · Court review of final administrative action; exhaustion of administrative remedies.
- 42 CFR 9.1 · Applicability and purpose.
- 42 CFR 9.2 · Definitions.
- 42 CFR 9.3 · Sanctuary policies and responsibilities.
- 42 CFR 9.4 · Physical facility policies and design.
- 42 CFR 9.5 · Chimpanzee ownership, fees, and studies.
- 42 CFR 9.6 · Animal care, well-being, husbandry, veterinary care, and euthanasia.
- 42 CFR 9.7 · Reproduction.
- 42 CFR 9.8 · Animal records.
- 42 CFR 9.9 · Facility staffing.
- 42 CFR 9.10 · Occupational Health and Safety Program (OHSP) and biosafety requirements.
- 42 CFR 9.11 · Animal transport.
- 42 CFR 9.12 · Compliance with the Standards of Care, and USDA and PHS policies and regulations.
- 42 CFR 9.13 · Other federal laws, regulations, and statutes that apply to the sanctuary.
- 42 CFR 10.1 · Purpose.
- 42 CFR 10.2 · Summary of 340B Drug Pricing Program.
- 42 CFR 10.3 · Definitions.
- 42 CFR 10.10 · Ceiling price for a covered outpatient drug.
- 42 CFR 10.11 · Manufacturer civil monetary penalties.
- 42 CFR 10.20 · 340B Administrative Dispute Resolution Panel.
- 42 CFR 10.21 · Claims.
- 42 CFR 10.22 · Covered entity information and document requests.
- 42 CFR 10.23 · 340B ADR Panel decision process.
- 42 CFR 10.24 · 340B ADR Panel decision reconsideration process.
- 42 CFR 10.25 · Severability.
- 42 CFR 11.2 · What is the purpose of this part?
- 42 CFR 11.4 · To whom does this part apply?
- 42 CFR 11.6 · What are the requirements for the submission of truthful information?
- 42 CFR 11.8 · In what format must clinical trial information be submitted?
- 42 CFR 11.10 · What definitions apply to this part?
- 42 CFR 11.20 · Who must submit clinical trial registration information?
- 42 CFR 11.22 · Which applicable clinical trials must be registered?
- 42 CFR 11.24 · When must clinical trial registration information be submitted?
- 42 CFR 11.28 · What constitutes clinical trial registration information?
- 42 CFR 11.35 · By when will the NIH Director post clinical trial registration information submitted under § 11.28?
- 42 CFR 11.40 · Who must submit clinical trial results information?
- 42 CFR 11.42 · For which applicable clinical trials must clinical trial results information be submitted?
- 42 CFR 11.44 · When must clinical trial results information be submitted for applicable clinical trials subject to § 11.42?
- 42 CFR 11.48 · What constitutes clinical trial results information?
- 42 CFR 11.52 · By when will the NIH Director post submitted clinical trial results information?
- 42 CFR 11.54 · What are the procedures for requesting and obtaining a waiver of the requirements for clinical trial results information submission?
- 42 CFR 11.60 · What requirements apply to the voluntary submission of clinical trial information for clinical trials of FDA-regulated drug products (including biological products) and device products?
- 42 CFR 11.62 · What requirements apply to applicable clinical trials for which submission of clinical trial information has been determined by the Director to be necessary to protect the public health?
- 42 CFR 11.64 · When must clinical trial information submitted to ClinicalTrials.gov be updated or corrected?
- 42 CFR 11.66 · What are potential legal consequences of not complying with the requirements of this part?
- 42 CFR 12.1 · Temporary extension of certain COVID-19 telemedicine flexibilities for prescription of controlled medications.
- 42 CFR 12.2 · [Reserved]
- 42 CFR 12.3 · Telemedicine prescribing of schedule III-V medications for the treatment of Opioid Use Disorder.
- 42 CFR 12.4 · Telemedicine prescribing of schedule II-V medications by the Department of Veterans Affairs practitioners.
- 42 CFR 21.1 · Meaning of terms.
- 42 CFR 21.21 · Meaning of terms.
- 42 CFR 21.22 · Submission of application and evidence of qualifications.
- 42 CFR 21.23 · False statements as disqualification.
- 42 CFR 21.24 · Physical examinations.
- 42 CFR 21.25 · Eligibility; junior assistant grade.
- 42 CFR 21.26 · Eligibility; assistant grade.
- 42 CFR 21.27 · Eligibility; senior assistant grade.
- 42 CFR 21.28 · Age requirements, Regular Corps, senior assistant grade and below.
- 42 CFR 21.29 · Eligibility; grades above senior assistant grade.
- 42 CFR 21.30 · Determination of creditable years of educational and professional training and experience.
- 42 CFR 21.31 · Eligibility; all grades; academic and professional education and professional training and experience.
- 42 CFR 21.32 · Boards; appointment of; powers and duties.
- 42 CFR 21.33 · General service.
- 42 CFR 21.34 · Certification by candidate; requirement of new physical examination.
- 42 CFR 21.41 · Professional examinations, holding of; subjects to be included.
- 42 CFR 21.42 · Examinations; junior assistant, assistant, or senior assistant grade.
- 42 CFR 21.43 · Examination; full grade and above.
- 42 CFR 21.44 · Clinical or other practical demonstration.
- 42 CFR 21.45 · Rating values.
- 42 CFR 21.46 · Merit roll.
- 42 CFR 21.47 · Examination; anticipation of meeting qualifications.
- 42 CFR 21.51 · Appointment of officers having specialized training or experience in administration and management.
- 42 CFR 21.52 · Waiver of entrance qualifications for original appointment in time of war or national emergency.
- 42 CFR 21.53 · Examination.
- 42 CFR 21.54 · Students.
- 42 CFR 21.55 · Appointment to higher grades; candidates exceptionally qualified in specialized fields.