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- VOLUME A-1 (Title 10)
- Chapter II - Administrative Rules And Regulations
- SubChapter D - Laboratories
- Part 55 - Approval Of Laboratories
- SubPart 55-1 - Approval of Laboratories and Institutions for Use of Living Animals and for Requisition and Allocation of Animals From Pounds
- Title: Section 55-1.4 - Responsibility
Title: Section 55-1.4 - Responsibility
USE OF ANIMALS
55-1.4 Responsibility.
(a) The individual whose name appears on the certificate of approval shall be responsible for all of the experimentation that involves the use of living animals in the designated laboratory or institution. Such individual shall designate one person to be in charge of animal care. That person shall be responsible for the animals' care regardless of whether that person is physically within or away from the laboratory or institution.
(b) The laboratory or institution shall have an animal care committee which shall be responsible for the review of the propriety of the procedures used and the scientific justification for the use of animals in experiments, tests, and investigations, including educational demonstrations.
Volume
VOLUME A-1 (Title 10)
- VOLUME A-1 (Title 10)
- Chapter II - Administrative Rules And Regulations
- SubChapter A - Vital Records and Personal Information
- Part 34 - Health Care Practitioner Referrals and Laboratory Business Practices
- SubPart 34-1 - Health Care Practitioner Referrals
- Section 34-1.1 - Title
- Section 34-1.2 - Definitions
- Section 34-1.3 - Referrals prohibited
- Section 34-1.4 - Disclosure: Clinical laboratory services, pharmacy services or x-ray
- Section 34-1.5 - Disclosure: other health or health related items or services.
- Section 34-1.6 - Disclosure form
- Section 34-1.7 - Exceptions from compensation arrangement prohibitions.
- SubPart 34-2 - Laboratory Business Practices
- Section 34-2.1 - Title
- Section 34-2.2 - Definitions
- Section 34-2.3 - Prohibited business practices by health services purveyors -- general
- Section 34-2.4 - Prohibited business practices by clinical laboratories
- Section 34-2.5 - Equipment, supplies and services
- Section 34-2.6 - Space
- Section 34-2.7 - Employees
- Section 34-2.8 - Professional courtesy
- Section 34-2.9 - Computers
- Section 34-2.10 - Waste disposal
- Section 34-2.11 - Recall letters and reporting of test results
- Section 34-2.12 - Waiver of co-payments, co-insurance, deductibles and fees
- Section 34-2.13 - Direct billing
- Section 34-2.14 - Financial relationship
- Section 34-2.15 - Loans
- Section 34-2.16 - Compliance
- Section 34-2.17 - Exclusions
- SubPart 34-1 - Health Care Practitioner Referrals
- Part 35 - Vital Records
- Section 35.1 - Searches and certifications without fees
- Section 35.2 - Birth records; confidential information
- Section 35.3 - Fetal death; confidential information
- Section 35.4 - Death records; disclosure
- Section 35.5 - Genealogical research; method of disclosure; searches
- Section 35.6 - Adoption Information Registry
- Section 35.7 Reserved
- Section 35.8 - Birth and Death Certification; Form and Content
- Section 35.9 Reserved
- Section 35.10 Reserved
- Section 35.11 Reserved
- Section 35.12 Reserved
- Section 35.13 Reserved
- Section 35.14 Reserved
- Section 35.15 - Wallet-size certification of birth; fee
- Part 36 - Delayed Registration Of An Unrecorded Birth
- Section 36.1 - Definitions
- Section 36.5 - Certificate made by attendant at birth
- Section 36.6 - Certificate made by parent
- Section 36.7 - Making of the certificate of birth in all other cases
- Section 36.10 - Official certification that record of birth is not on file required
- Section 36.11 - Proof required in support of application for delayed registration of an unrecorded birth
- Part 37 - Handling Of Bodies Of Persons Dying On Common Carriers
- Part 38 - Information Obtained Under Provisions Of State Or Federal Laws
- Part 34 - Health Care Practitioner Referrals and Laboratory Business Practices
- SubChapter B - State Aid and Funding
- Part 39 REPEALED
- Part 40 - State Aid For Public Health Services: Counties And Cities
- SubPart 40-1 - Application and Payment
- Section 40-1.0 - Applications for State aid
- Section 40-1.10 - Performance and accountability; reporting
- Section 40-1.20 - Personnel
- Section 40-1.30 - Maintenance of effort
- Section 40-1.40 - Limitation on State Aid
- Section 40-1.41 - Withholding of State Aid
- Section 40-1.50 - Fees and revenue; quarterly reporting
- Section 40-1.51 - Fees and revenue; services for which fees are charged
- Section 40-1.52 - Fees and revenue; calculation
- Section 40-1.53 - Fees and revenue; deduction and offset
- Section 40-1.60 - Submission of claims
- Section 40-1.61 - Method of payment
- Section 40-1.62 - Claims and method of payment; State Aid for physically handicapped children
- SubPart 40-2 - Performance Standards and Minimum Requirements for Core Public Health Services
- GENERAL PROVISIONS
- FAMILY HEALTH
- COMMUNICABLE DISEASE CONTROL
- Section 40-2.20 - Sexually Transmitted Diseases (STDs) and Human Immunodeficiency Virus (HIV); performance standards
- Section 40-2.21 - Tuberculosis; performance standards
- Section 40-2.22 - Communicable disease control; performance standards
- Section 40-2.23 - Immunization; performance standards
- Section 40-2.24 - REPEALED
- CHRONIC DISEASE PREVENTION
- COMMUNITY HEALTH ASSESSMENT
- ENVIRONMENTAL HEALTH
- Section 40-2.50 - Public water supply protection; performance standards
- Section 40-2.51 - Environmental radiation protection; performance standards
- Section 40-2.52 - Community environmental health and food protection; performance standards
- Section 40-2.53 - Realty subdivisions; performance standards
- Section 40-2.54 - Individual water and sewage systems; performance standards
- Section 40-2.55 - Public health nuisances; performance standards
- Section 40-2.56 - Injury prevention and control; performance standards
- Section 40-2.57 - Environmental and occupational health exposure investigation, assessment and response; performance standards
- Section 40-2.58 - Lead poisoning prevention; performance standards
- Section 40-2.59 - Cooling Towers; performance standards
- ENVIRONMENTAL HEALTH – ONLY WHERE AUTHORIZED
- Section 40-2.60 - Authorized radioactive materials licensing and inspection program; performance standards
- Section 40-2.61 - Authorized radiation-producing equipment inspection program; performance standards
- Section 40-2.62 - Authorized tanning facilities licensing and inspection program; performance standards
- EMERGENCY PREPAREDNESS AND RESPONSE
- SubPart 40-3 - REPEALED
- SubPart 40-4 - Fee and Revenue Plan for Departmental Services
- SubPart 40-1 - Application and Payment
- Part 41 - Grants For School Health Projects
- Part 42 - State Aid For Public Health Laboratory Services: Counties And Cities
- Part 43 - State Aid For Tuberculosis and Uninsured Care Programs
- SubPart 43-1 - STATE AID FOR TUBERCULOSIS
- STATE AID FOR TUBERCULOSIS
- REQUIREMENTS APPLYING TO PROVIDERS AS A CONDITION TO BEING ENTITLED TO PAYMENT FOR TUBERCULOSIS HEALTH CARE SERVICES
- AUTHORIZATION
- PROVIDER CLAIM FOR PAYMENT AND EFFORTS TO DETERMINE AVAILABILITY OF THIRD-PARTY PAYERS
- RESPONSIBILITY FOR PAYMENT FOR SERVICES
- REQUIREMENTS APPLYING TO LOCAL HEALTH OFFICIALS FOR RECEIVING STATE AID FOR TUBERCULOSIS HEALTH CARE SERVICES
- LOCAL HEALTH UNIT RECORDS AND REPORTS TO STATE HEALTH DEPARTMENT
- SubPart 43-2 - Uninsured Care Programs
- Section 43-2.1 - Scope
- Section 43-2.2 - Definitions
- Section 43-2.3 - Confidentiality
- Section 43-2.4 - Use of the application form
- Section 43-2.5 - Eligibility for coverage
- Section 43-2.6 - Decision on eligibility
- Section 43-2.7 - Responsibility for prompt determination of eligibility
- Section 43-2.8 - Notification
- Section 43-2.9 - RESERVED
- Section 43-2.10 - Investigation
- Section 43-2.11 - Fraud and abuse
- Section 43-2.12 - Appeals
- Section 43-2.13 - Continuing eligibility
- Section 43-2.14 - Enrollment of providers.
- Section 43-2.15 - Audit and claim review
- Section 43-2.16 - Audits and recovery of overpayments
- Section 43-2.17 - Recoupment of overpayments
- Section 43-2.18 - Claims submission
- SubPart 43-1 - STATE AID FOR TUBERCULOSIS
- Part 44 - State Aid For Approved Vector Surveillance And Control Programs
- Section 44.10 - Purpose
- Section 44.20 - Definitions
- Section 44.30 - Eligibility for State aid
- Section 44.40 - Procedure for applying for State aid
- Section 44.41 - Additional requirements for localities applying for State aid
- Section 44.50 - Public health threat; determination
- Section 44.51 - Public health threat; risk assessment and declaration
- Section 44.60 - Standards for review and approval
- Section 44.61 - State aid reimbursement; vector surveillance and control
- Section 44.70 - Monitoring
- Section 44.80 - Claiming State aid
- Section 44.90 - State aid reimbursement amounts
- Part 45 - Cystic Fibrosis Health Care Program Adult Cystic Fibrosis Assistance Program
- Section 45.1 - Medical care and/or insurance premium reimbursement
- Section 45.2 - Definitions
- Section 45.3 - Eligibility criteria
- Section 45.4 - Qualified consultants
- Section 45.5 - Hospital and related medical care
- Section 45.6 - Payment for outpatient and related medical care
- Section 45.7 - Out-of-state care
- Section 45.8 - Accredited hospital
- Section 45.9 - Foreign diplomatic personnel
- Section 45.10 - Confidentiality
- Section 45.11 - Payor of last resort
- Part 46 - State Aid For Children and Youth with Special Health Care Needs
- Section 46.1 - Definition of medical service
- Section 46.2 - Conditions eligible
- Section 46.3 - Qualified consultants
- Section 46.4 - Accredited hospitals
- Section 46.5 - Maximum fees
- Section 46.6 - Inpatient hospital and related care
- Section 46.7 - Payment for outpatient and related service
- Section 46.8 - Out-of-state care
- Section 46.9 - Procedures and treatment at approved centers
- Section 46.10 - Financial investigators
- Section 46.11 - Foreign diplomatic personnel
- Part 47 - New York State Health Service Corps/Obstetric And Pediatric Practitioner Incentive Demonstration Program
- SubPart 47-1 - New York State Health Service Corps
- Section 47-1.1 - Definitions
- Section 47-1.2 - Eligibility for an award
- Section 47-1.3 - Selection of award recipients
- Section 47-1.4 - Maintaining eligibility for awards
- Section 47-1.5 - Award rescission and deferrals
- Section 47-1.6 - Service obligation
- Section 47-1.7 - Service obligation: deferrals and waivers
- Section 47-1.8 - Default
- Section 47-1.9 - Administration
- SubPart 47-2 - Obstetric and Pediatric Practitioner Incentive Demonstration Program
- SubPart 47-3 - DESIGNATION OF UNDERSERVED AREAS
- SubPart 47-4 - Resident Loan Repayment Program.
- SubPart 47-5 - Physican Loan Repayment Program
- SubPart 47-6 - Primary Care Practitioner Scholarship Program
- Section 47-6.1 - Definitions
- Section 47-6.2 - Eligibility for an award
- Section 47-6.3 - Selection of recipients
- Section 47-6.4 - Maintaining eligibility for an award
- Section 47-6.5 - Award rescission and deferrals
- Section 47-6.6 - Service obligation
- Section 47-6.7 - Service obligation: deferrals and waivers
- Section 47-6.8 - Default
- Section 47-6.9 - Administration
- SubPart 47-1 - New York State Health Service Corps
- Part 48 - Palliative Care Certified Medical Schools and Residency Programs
- Part 49 - Funding For Family Practice Residency Training Programs
- SubChapter C - Access to Records
- Part 50 - Funding For Family Practice Residency Training Programs
- SubPart 50-1 - Access to Records
- Section 50-1.1 - Statement of purpose
- Section 50-1.2 - Definitions
- Section 50-1.3 - Times and places for inspecting records
- Section 50-1.4 - Persons from whom records may be obtained
- Section 50-1.5 - Fees for copying records
- Section 50-1.6 - Availability of department records
- Section 50-1.7 - Procedures governing inspection and copying of records
- Section 50-1.8 - Trade secrets
- Section 50-1.9 - Appeals of denial of access to records
- SubPart 50-2 - Access to or Correction/Amendment of Records of the Department of Health Subject to the Personal Privacy Protection Law
- Section 50-2.1 - Statement of purpose
- Section 50-2.2 - Definitions
- Section 50-2.3 - Times, places for inspecting records and means for verifying the identity of a data subject
- Section 50-2.4 - Persons from whom records may be obtained
- Section 50-2.5 - Fees for copying records
- Section 50-2.6 - Procedures governing the inspection and copying of records
- Section 50-2.7 - Appeals of denial of access to records
- Section 50-2.8 - Procedures governing the correction or amendment of records
- Section 50-2.9 - Appeals of denial of correction or amendment of records
- SubPart 50-3 - Access to Patient Information
- Section 50-3.1 - Application
- Section 50-3.2 - Definitions
- Section 50-3.3 - Medical record access review committee
- Section 50-3.4 - Notification of patient rights
- Section 50-3.5 - Decisions
- Section 50-3.6 - Confidentiality
- Section 50-3.7 - REPEALED
- Section 50-3.8 - REPEALED
- Section 50-3.9 - REPEALED
- Section 50-3.10 - REPEALED
- SubPart 50-4 - Intra-Agency Access to and Disclosure of Personal Health-Related Information
- SubPart 50-1 - Access to Records
- Part 51 - Uniform Hearing Procedures
- Section 51.1 - Applicability
- Section 51.2 - Definitions
- Section 51.3 - Notice of hearing and statement of charges
- Section 51.4 - Adjournment
- Section 51.5 - Answer or responsive pleading
- Section 51.6 - Amendment of pleadings
- Section 51.7 - Service of papers
- Section 51.8 - Disclosure
- Section 51.9 - Hearing officer
- Section 51.10 - Stipulations and consent orders
- Section 51.11 - The hearing
- Section 51.12 - Hearing officer's report
- Section 51.13 - Filing of exceptions
- Section 51.14 - Final determination and order
- Section 51.15 - Waiver of rules
- Section 51.16 - Administrative hearings (one-year time frame)
- Section 51.17 - Disqualification for bias
- Part 52 - Tissue Banks And Nontransplant Anatomic Banks
- SubPart 52-1 - Definitions
- SubPart 52-2 - Tissue Banks and NonTransplant Anatomic Banks-Licensure
- Section 52-2.1 - Licensure
- Section 52-2.2 - Provisional licensure
- Section 52-2.3 - Ownership or controlling interest reporting requirements
- Section 52-2.4 - Special criteria for tissue bank licensure
- Section 52-2.5 - License issuance and denial
- Section 52-2.6 - Financial disclosure and fees for services
- Section 52-2.7 - Administration and direction
- Section 52-2.8 - Administration of a tissue transplantation facility
- Section 52-2.9 - Required records
- Section 52-2.10 - Compliance with standards
- SubPart 52-3 - General Technical Standards for Tissue Banks
- Section 52-3.1 - Compliance with FDA regulations and manufacturers' instructions
- Section 52-3.2 - Sterilization of instruments
- Section 52-3.3 - Qualifications of donors
- Section 52-3.4 - Selection and testing requirements for tissue donors
- Section 52-3.5 - Quality assurance and safety requirements
- Section 52-3.6 - HIV antibody testing and notification
- Section 52-3.7 - Reporting requirements
- Section 52-3.8 - Special circumstances
- SubPart 52-4 - Cardiovascular Tissue Banks
- Section 52-4.1 - Definition
- Section 52-4.2 - Construction
- Section 52-4.3 - Tissue procurement services
- Section 52-4.4 - Donor qualifications
- Section 52-4.5 - Retrieval of tissue
- Section 52-4.6 - Tissue processing facilities
- Section 52-4.7 - Required laboratory tests on donor and donated tissue
- Section 52-4.8 - Processing and storage of tissue
- Section 52-4.9 - Distribution of tissue products
- Section 52-4.10 - Required records of tissue acquisition, testing, processing and storage
- Section 52-4.11 - Records to be kept by a tissue transplantation facility
- Section 52-4.12 - Disposition of unused tissue
- Section 52-4.13 - Tissue storage facilities
- SubPart 52-5 - Musculoskeletal Tissue Banks
- Section 52-5.1 - Definitions
- Section 52-5.2 - Construction
- Section 52-5.3 - Tissue procurement services
- Section 52-5.4 - Donor qualifications
- Section 52-5.5 - Retrieval of tissue
- Section 52-5.6 - Tissue processing facilities
- Section 52-5.7 - Required laboratory tests on donors and donated tissue
- Section 52-5.8 - Processing and storage of tissue
- Section 52-5.9 - Distribution of tissue products
- Section 52-5.10 - Required records of tissue acquisition, testing, processing and storage
- Section 52-5.11 - Records to be kept by the tissue transplantation facility
- Section 52-5.12 - Disposition of unused tissue
- Section 52-5.13 - Tissue storage facilities
- SubPart 52-6 - Skin Banks
- Section 52-6.1 - Definitions
- Section 52-6.2 - Construction
- Section 52-6.3 - Tissue procurement services
- Section 52-6.4 - Donor qualifications
- Section 52-6.5 - Retrieval of tissue
- Section 52-6.6 - Tissue processing facilities
- Section 52-6.7 - Required laboratory tests on donors and donated tissue
- Section 52-6.8 - Processing and storage of tissue
- Section 52-6.9 - Distribution of tissue products
- Section 52-6.10 - Required records of tissue acquisition, testing, processing and storage
- Section 52-6.11 - Records to be kept by a tissue transplantation facility
- Section 52-6.12 - Disposition of unused tissue
- Section 52-6.13 - Tissue storage facilities
- SubPart 52-7 - Eye Banks
- Section 52-7.1 - Definitions
- Section 52-7.2 - Construction
- Section 52-7.3 - Tissue procurement services
- Section 52-7.4 - Donor qualifications
- Section 52-7.5 - Retrieval of tissue
- Section 52-7.6 - Tissue processing facilities
- Section 52-7.7 - Required laboratory tests on donors and donated tissue
- Section 52-7.8 - Processing and storage of tissue
- Section 52-7.9 - Distribution of tissue products
- Section 52-7.10 - Required records of tissue acquisition, testing, processing and
- Section 52-7.11 - Laboratory tests to be performed prior to tissue transplantation.
- Section 52-7.12 - Records to be kept by a tissue transplantation facility
- Section 52-7.13 - Disposition of unused tissue
- SubPart 52-8 - Reproductive Tissue Banks
- Section 52-8.1 - Definitions
- Section 52-8.2 - Licensure
- Section 52-8.3 - Administrative responsibility
- Section 52-8.4 - Direction and medical direction
- Section 52-8.5 - Donor qualifications
- Section 52-8.6 - Required laboratory tests
- Section 52-8.7 - Collection, storage and disposition of reproductive tissue
- Section 52-8.8 - Informed consent
- Section 52-8.9 - Required records
- Section 52-8.10 - Quality assurance and safety
- Section 52-8.11 - Compliance with standards
- SubPart 52-9 - Human Milk Banks
- Section 52-9.1 - Definitions
- Section 52-9.2 - Construction
- Section 52-9.3 - Administrative responsibility
- Section 52-9.4 - Medical direction
- Section 52-9.5 - Donor qualifications
- Section 52-9.6 - Collection and storage of human milk
- Section 52-9.7 - Maintenance of records
- Section 52-9.8 - Distribution of human milk
- SubPart 52-10 - Hematopoietic Progenitor Cell Banks
- SubPart 52-11 - Nontransplant Anatomic Banks
- Section 52-11.1 - Definitions
- Section 52-11.2 - Construction
- Section 52-11.3 - Informed Consent
- Section 52-11.4 - Retrieval and acquisition of nontransplant anatomic parts
- Section 52-11.5 - Use of nontransplant anatomic parts
- Section 52-11.6 - Disposition of nontransplant anatomic parts
- Section 52-11.7 - Safety
- Section 52-11.8 - Reporting Requirements
- Part 53 - Drinking Water State Revolving Fund
- Section 53.1 - Purpose, scope and applicability
- Section 53.2 - Definitions
- Section 53.3 - Pre-application procedure
- Section 53.4 - Priority ranking system scoring criteria
- Section 53.5 - Priority ranking and Intended Use Plan
- Section 53.6 - General project requirements
- Section 53.7 - Remedies
- Section 53.8 - Severability
- Part 50 - Funding For Family Practice Residency Training Programs
- SubChapter D - Laboratories
- Part 54 - Requirements For Self-Defense Spray Devices
- Part 55 - Approval Of Laboratories
- SubPart 55-1 - Approval of Laboratories and Institutions for Use of Living Animals and for Requisition and Allocation of Animals From Pounds
- SubPart 55-2 - Approval of Laboratories Performing Environmental Analysis
- Section 55-2.1 - Definitions
- Section 55-2.2 - Certificates of approval
- Section 55-2.3 - Application for approval
- Section 55-2.4 - Approval criteria
- Section 55-2.5 - Department approval of methods
- Section 55-2.6 - Denial, suspension and revocation of department approval
- Section 55-2.7 - Laboratory on-site assessments
- Section 55-2.8 - Proficiency testing
- Section 55-2.9 - Recognition of other state regulatory programs
- Section 55-2.10 - Technical director: qualifications and responsibilities
- Section 55-2.11 - Quality assurance officer: qualifications and responsibilities
- Section 55-2.12 - Contract laboratory protocol personnel: qualifications
- Section 55-2.13 - Requirements for laboratories engaged in testing for critical agents in environmental samples
- Section 55-2.14 - Additional requirements for laboratories engaged in testing for critical agents in environmental samples using autonomous detection systems
- Section 55-2.15 - Repealed by the Office of Cannabis Management emergency regulation effective on August 16, 2022
- SubPart 55-3 - Environmental Laboratory Approval Fee
- Section 55-3.1 - Definitions
- Section 55-3.2 - Annual approval fee
- Section 55-3.3 - Annual report
- Section 55-3.4 - Method of payment of approval fee
- Section 55-3.5 - Suspension or renewal of certificate of approval
- Section 55-3.6 - Annual cost adjustment
- Section 55-3.7 - Approval fee computation
- Section 55-3.8 - Inspection fee
- Section 55-3.9 - Environmental laboratory approval program difficulty factors
- Part 57 - Conditions Under Which A Dog Actively Immunized Against Rabies May Be At Large In Designated Areas Certified For Rabies
- Part 58 - Clinical Laboratories And Blood Banks
- SubPart 58-1 - Clinical Laboratories
- Section 58-1.1 - Permit
- Section 58-1.2 - Laboratory director
- Section 58-1.3 - Clinical laboratory and blood bank supervision
- Section 58-1.4 - Qualifications of laboratory supervisor
- Section 58-1.5 - Duties and qualifications of clinical laboratory technical personnel
- Section 58-1.6 - Physical facilities
- Section 58-1.7 - Acceptance of specimens
- Section 58-1.8 - Results of tests to be reported only to physicians or other authorized persons
- Section 58-1.9 - Testing to be done on premises except in certain instances
- Section 58-1.10 - Specimens: identification and examination
- Section 58-1.11 - Reports and records
- Section 58-1.12 - Cytopathology standards and quality assurance
- Section 58-1.13 - General requirements for performance of anatomic pathology and cytopathology procedures
- Section 58-1.14 - Reporting of certain communicable diseases
- SubPart 58-2 - Blood Banks and Laboratories Performing Immunohematology Testing
- Section 58-2.1 - Definitions
- Section 58-2.2 - Qualifications of donors
- Section 58-2.3 - Required laboratory tests for donated blood
- Section 58-2.4 - Collection of blood
- Section 58-2.5 - Sterilization of instruments
- Section 58-2.6 - Collection and handling of blood for subsequent allogeneic or autogeneic transfusion
- Section 58-2.7 - Immunohematology testing
- Section 58-2.8 - Standard operating procedures
- Section 58-2.9 - Issuance of blood, blood components and derivatives
- Section 58-2.10 - Required records and confidentiality
- Section 58-2.11 - Records to be kept when blood is collected for autogeneic or allogeneic transfusion
- Section 58-2.12 - Records to be kept when blood, blood components or derivatives are issued for allogeneic or autogeneic transfusion
- Section 58-2.13 - Distribution facilities
- Section 58-2.14 - RESERVED
- Section 58-2.15 - Collection of blood components by apheresis
- Section 58-2.16 - Required standards for transfusion
- Section 58-2.17 - Laboratory tests to be performed prior to allogeneic or autogeneic transfusion
- Section 58-2.18 - Records to be kept when blood or blood component transfusions are performed
- Section 58-2.19 - Records to be kept when derivatives are infused
- Section 58-2.20 - Ambulance Transfusion Services
- Section 58-2.21 - Limited transfusion services
- Section 58-2.22 Reserved
- Section 58-2.23 - HIV-1 and HIV-2 antibody testing results
- Section 58-2.24 - Disposal of untransfused and expired blood units
- Section 58-2.25 - Intraoperative and postoperative blood recovery and normovolemic hemodilution
- Section 58-2.26 - Exceptions
- Section 58-2.27 - Reinfusion procedures
- Section 58-2.28 - Incorporation by reference
- SubPart 58-3 - Clinical Laboratory Inspection and Reference Fees
- Section 58-3.1 - Definitions
- Section 58-3.2 - Laboratory inspection and reference fee
- Section 58-3.3 - Reporting
- Section 58-3.4 - Quarterly payments
- Section 58-3.5 - Suspension or nonrenewal of laboratory permit
- Section 58-3.6 - Fees
- Section 58-3.7 - Gross annual receipts
- Section 58-3.8 - Out-of-state laboratory seeking permit
- Section 58-3.9 - Effective dates
- SubPart 58-4 - Source Plasma Donation Centers
- SubPart 58-5 - Hematopoietic Progenitor Cell Banks
- Section 58-5.1 - Definitions
- Section 58-5.2 - General requirements.
- Section 58-5.3 - Hematopoietic progenitor cell procurement
- Section 58-5.4 - Donor qualifications.
- Section 58-5.5 - Sterilization of instruments
- Section 58-5.6 - Collection and handling of hematopoietic progenitor cells
- Section 58-5.7 - Hematopoietic progenitor cell processing facilities
- Section 58-5.8 - Required records.
- Section 58-5.9 - Quality assurance and safety requirements
- Section 58-5.10 - Compliance with standards
- Section 58-5.11 - Licensure
- Section 58-5.12 - Special circumstances
- SubPart 58-6 - Repealed
- SubPart 58-7 - Repealed
- SubPart 58-8 - Human Immunodeficiency Virus (HIV) Testing
- SubPart 58-1 - Clinical Laboratories
- Part 59 - Chemical Analyses of Blood, Urine, Breath or Saliva for Alcoholic Content
- Section 59.1 - Definitions
- Section 59.2 - Techniques and methods for determining blood and urine alcohol
- Section 59.3 - Blood, urine and saliva alcohol analysis; permits
- Section 59.4 - Breath analysis instruments
- Section 59.5 - Breath analysis; techniques and methods
- Section 59.6 - Breath analysis permit program
- Section 59.7 - Breath analysis operator permits
- Section 59.8 - Revocation or suspension of permits
- Section 59.9 - Technical supervisor; qualifications and certification
- Section 59.10 - Certification criteria for ignition interlock devices
- Section 59.11 - Testing of ignition interlock devices
- Section 59.12 - Continued ignition interlock device certification
- SubChapter A - Vital Records and Personal Information
- Chapter II - Administrative Rules And Regulations