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- VOLUME A-1 (Title 10)
- Chapter II - Administrative Rules And Regulations
- SubChapter D - Laboratories
- Part 58 - Clinical Laboratories And Blood Banks
- Title: SubPart 58-3 - Clinical Laboratory Inspection and Reference Fees
Title: SubPart 58-3 - Clinical Laboratory Inspection and Reference Fees
Effective Date
12/23/1985
Statutory Authority
Public Health Law, Section 576(4)
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