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SSBA Regulatory Scheme Road Show. Welcome and Introductions. Speakers. Dr Gary Lum – Assistant Secretary Health Emergency Management Branch (DoHA) Wendy Barry – Assistant Director Laboratory Capacity & Regulation Section (DoHA) Nicole Hutchins – Assistant Director a/g

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SSBA Regulatory Scheme Road Show

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SSBA Regulatory SchemeRoad Show


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Welcome and Introductions


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Speakers

  • Dr Gary Lum – Assistant Secretary

    • Health Emergency Management Branch (DoHA)

  • Wendy Barry – Assistant Director

    • Laboratory Capacity & Regulation Section (DoHA)

  • Nicole Hutchins – Assistant Director a/g

    • Laboratory Capacity & Regulation Section (DoHA)

  • Andrew Straffon

    • Australian CBRN Data Centre, AFP

  • Jurisdictional Representative


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Office of Health Protection


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Health Emergency Management


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Program Outline

  • Setting the Scene

  • International Obligations

  • Technical Feasibility and Risk Report

  • Jurisdictional Context

  • National Health Security Act 2007

  • National Health Security Regulations 2008

  • SSBA Standards

  • Reporting Requirements and Timeframes

  • The Inspection Process

  • SSBA Publications


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SSBA Road ShowObjectives

  • To raise awareness and provide an overview of the SSBA Regulatory Scheme


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Evaluation

  • Evaluation forms have been provided

  • We would like you to complete the evaluation form

  • You may choose to complete this form during the course of the day


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Setting the Scene


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Outline

  • Introduction

  • The COAG Report


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Introduction

  • Terrorism

    • Increased global risk of terrorism

      • 11 September 2001

      • Anthrax attacks in 2001

  • Biological Weapons Convention

    • Expanding knowledge of biotechnology

    • Legitimate research and the dual use dilemma (legitimate and malicious use of the same agent)


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COAG Review

  • 2002

    • COAG review of hazardous materials

  • 2006

    • Banks Report

  • 2007

    • COAG Report recommended a regulatory scheme for security-sensitive biological agents (SSBAs)


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The COAG Report

  • Purpose

  • Recommendations of the COAG Report

    • Risk management was applied

    • Balance between counter-terrorism concerns and industry interests

    • Maintain access to SSBAs for those with legitimate need


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International Obligations Presented byThe Department of Foreign Affairs


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Technical Feasibility and Risk Report Presented byThe Australian CBRN Data Centre


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Jurisdictional Context


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National Health SecurityLegislation


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Outline

  • Introduction

  • National Health Security Act 2007

  • Amendments to the NHS Act

  • National Health Security Regulations 2008

  • Amendments to the NHS Regulations

  • Exemptions

  • List of SSBA


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National Health Security Act 2007

  • The National Health Security Bill was passed in Parliament on 20 September 2007

  • Commencement

    • Part 2 - commenced on 29 March 2008

    • Part 3 - commenced on 31 January 2009


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National Health Security Act 2007 (2)

Two main operative parts

  • Part 2:

    • Surveillance arrangements to support responses to national and international public health emergencies

    • Assist repatriation of victims of overseas mass casualty events

  • Part 3:

    • Establishes the regulation of security sensitive biological agents (SSBAs)


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SSBA Regulatory SchemePart 3 of the NHS Act

  • How SSBAs will be handled

  • Who will be regulated

  • Who is exempt

  • Information collection process

  • Checking of information


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Role of the Secretary

  • Secretary of the Australian Government’s Department of Health and Ageing

  • Responsible for the administration and enforcement of the NHS Act. For Example:

    • Deciding to register an entity on the National Register

    • Directing an entity to dispose of SSBAs or to arrange for that disposal


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Legitimate Purpose

  • The NHS Act defines what is a ‘legitimate purpose’ (s41)

  • Legitimate purposes are:

    • Scientific or medical work

    • Diagnostic analysis of samples

    • Forensics

    • Research

  • Temporary Registration


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Amendments to the Act

  • Consultation on the Security Sensitive Biological Agents (SSBA) Regulatory Scheme has identified measures to enhance the operation of Part 3 of the NHS Act

  • Introduced 24 June 2009

  • Aim for passing Spring 2009


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Amendments to the Act (2)

  • Emergency disease situation

  • Handling suspected SSBAs

  • Inspector powers

  • Reporting to law enforcement

  • ‘Nil’ reporting

  • Cancellation of registration

  • New definition of ‘biological agents’


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Amendments to the Act Emergency Disease Situation

  • Flexible - not to impede diagnosis and treatment

  • Minister able to suspend some or all regulatory obligations for an SSBA

  • Legislative instrument which may be varied or revoked, to address the situation

  • Advised by relevant experts

  • Maintain adequate controls


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Amendments to the ActHandling a Suspected SSBA

  • Regulation of biological agents suspected of being SSBAs

  • Usual testing processes

  • Presumptive identification of an SSBA

  • Requirement to report:

    • Destruction

    • Confirmatory testing

  • Comply with relevant SSBA Standards

  • Reporting requirements


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Amendments to the ActCancellation of Registration

  • No longer handling SSBA

  • Entities not expecting to handle SSBAs in future

  • Application to the Secretary

  • No longer subject to regulatory obligations


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National Health Security Regulations 2008

  • The NHS Act enables regulations to provide further specific detail for the SSBA Regulatory Scheme

  • Work in conjunction with the SSBA Standards to provide operational detail


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What is in the Regulations?

  • The Regulations deal with:

    • Additional detail for inclusion on the National Register (3.1)

    • Additional reportable events (3.4)

    • Time frames for reporting (3.5)

    • Agencies that the Secretary may provide a report to (3.71)

    • Inspector identity cards (3.70)

    • Exempt entities (3.2)


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Amendments to theNHS Regulations

  • Required as a result of the NHS Act Amendments

    • Reporting reportable events to police

    • ‘Nil’ Reporting

  • Expected to be finalised December 2009


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Exemptions

  • NHS Act s40

    • Transport companies

  • NHS Regulations (s3.2)

    • Border security or law enforcement agencies

    • Depot or warehouse licence holders

    • A person or animal who is infected by an SSBA


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List of SSBA

  • NHS Act s31–s34

  • 12 Tier 1 SSBA

    • Tier 1 regulation commenced on 31 January 2009

  • 10 Tier 2 SSBA

    • Tier 2 agents will be regulated from January 2010


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Abrin (5mg)

Bacillus anthracis (Anthrax—virulent forms)

Botulinum toxin (0.5mg)

Ebolavirus

Foot-and-mouth disease virus

Highly pathogenic influenza virus, infecting humans (such as 1918 pandemic Influenzavirus A and Influenzavirus A H5N1)

Marburgvirus

Ricin (5mg)

Rinderpest virus

SARS coronavirus

Variola virus (Smallpox)

Yersinia pestis (Plague)

Tier 1 SSBA


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African swine fever virus

Capripoxvirus (Sheep pox virus and Goat pox virus)

Classical swine fever virus

Clostridium botulinum (Botulism; toxin-producing strains)

Francisella tularensis (Tularæmia)

Lumpy skin disease virus

Peste-des-petits-ruminants virus

Salmonella Typhi (Typhoid fever)

Vibrio choleræ (Cholera) (serotypes O1 and O139 only)

Yellow fever virus (non-vaccine strains)

ProposedTier 2 SSBA


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ActivityQuiz

  • What part of the NHS Act covers the regulation of SSBA?

  • What are 2 amendments to the NHS Act?

  • What do the NHS Regulations do?

  • Name one exemption from the SSBA Regulatory Scheme?

  • When will Tier 2 SSBAs be regulated?


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Security Sensitive Biological Agent (SSBA) Standards


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Outline

  • Commencement

  • Part 1 Scope and Definitions

  • Part 2 Risk and Incident Management

  • Part 3 Personnel

  • Part 4 Physical security

  • Part 5 Information management

  • Part 6 Transport

  • Part 7 Inactivation and decontamination

  • Part 8 SSBA management system requirements

  • Part 9 Bibliography

  • Amendments


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SSBA Standards

  • SSBA Standards apply to any entity that handles one or more SSBAs and is not exempt

  • Specify compliance requirements

  • May be different requirements for Tier 1 SSBA versus Tier 2 SSBA

  • Registered but not handling no longer required to comply with the Standards


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Commencement

  • Part 1 and Part 2

    • commenced 31 January 2009

  • Remaining Parts

    • commenced 1 July 2009

  • Background checking has been removed from Part 3 of the Standards


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Part 1 Scope and Definitions

  • Sets out the overall scope of the Standards

  • Normative references regarding other legislation

  • Terms and definitions


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Part 2Risk and Incident Management

  • Minimum requirements for the risk assessment and risk management process

  • Minimum requirements for incident management and review

  • Risk assessment must be proactive rather than reactive


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Part 2Risk and Incident Management (2)

  • Risk assessment

    • Timing and scope

    • Hazard/risk identification

    • Risk assessment process

  • Risk management plan

  • Incident management

  • Review


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Tier 1 Versus Tier 2 Risk and Incident Management

  • Subclause 2.2.3 – Risk assessment process

    • Vulnerability analysis undertaken for Tier 1


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Risk and Incident Management Summary

  • Undertake a risk assessment and produce a risk management plan

  • Risk assessment and risk management process important for determining controls for rest of SSBA Standards

  • Incident management

  • Reviewing risk plans


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Part 3Personnel

  • Requirements for personnel management to assist in addressing the risk associated with human behaviour

  • Background checking has been removed from clauses 3.3 and 3.4


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Part 3Personnel (2)

  • Responsible Officers

  • Authorised persons

  • Approved persons

  • Recruitment

  • Training and competency

  • Behavioural factors

  • Exclusion


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Tier 1 Versus Tier 2Personnel

  • Clause 3.5 – Approved Persons

    • Escorted by an authorised person (Tier 1)

    • Supervised by an authorised person (Tier 2)

  • Clause 3.6 – Training Competency

    • Personal security awareness training (Tier 1)


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Personnel Summary

  • Responsible Officer

  • Deputy Responsible Officer

  • Authorised persons

  • Approved persons

  • Recruitment

  • Training and competency

  • Behavioural factors

  • Exclusion


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Part 4Physical Security

  • Limiting access to both the SSBA and the facility in which it is handled (including storage)

  • Requirements in part determined by risk assessment and risk management plan


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Part 4Physical Security (2)

  • Perimeter

  • Physical access controls

  • Storage of SSBAs


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Tier 1 Versus Tier 2Physical Security

  • Clause 4.3 ‑ Physical access controls

    • Two forms of access control (Tier 1)

      • One form for Tier 2

    • Prevent ‘tailgating’ (Tier 1)

    • Record date and time of entry and exit (Tier 1)

      • Records maintained for six months

    • Record date and time of entry (Tier 2)

      • Records maintained for three months

    • Access control systems tested

      • Six monthly (Tier 1)

      • Annually (Tier 2)


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Physical Security Summary

  • Perimeter controls

  • Physical access controls

    • Forms of control

    • Testing of controls

  • Storage of SSBAs


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Activity

  • Group 1

    • What could be considered a potential hazard associated with handling SSBAs?

    • What could you include in training for your staff members?

    • What forms of access control could you use?

  • Group 2

    • What could you include in your risk management plan?

    • Who might need to be an authorised person?

    • How could you store SSBA securely?

  • Group 3

    • When should you undertake a review of the risk management plan?

    • Who might need to be an approved person?

    • Who can access SSBA?


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Part 5Information Management

  • Identification of sensitive information and the handling of records

  • Sensitive information includes information about the SSBA, who can access the SSBA, risk and management plans, and storage records

  • Not intended to restrict the release of results from research, diagnosis or other legitimate uses


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Information Management (2)

  • Record Keeping

  • Information security

  • Inventory

  • Disposal of records


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Tier 1 Versus Tier 2Information Management

  • Clause 5.3 – Information security

    • Review process to control access to sensitive information

      • Six monthly (Tier 1)

      • Annually (Tier 2)

    • Secure storage and back up of sensitive information (Tier 1)

  • Clause 5.4 – Inventory

    • Records of inventory, receipt, holding, transport, and disposal kept for:

      • Minimum of five years (Tier 1)

      • Minimum of two years (Tier 2)


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Information Management Summary

  • Identify sensitive information

  • Maintain records

  • Secure sensitive information

  • Inventory

    • What SSBAs held

    • Where stored

  • Secure disposal of records


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Part 6Transport

  • Ensuring SSBAs are transported in a safe and secure manner

  • Regulatory requirements for the transport of dangerous goods

  • Apply to transport of SSBAs within Australia

  • Import and export permits


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Part 6Transport (2)

  • Compliance with dangerous goods transport requirements

  • Transport security

  • Verification and notification

  • Successful shipment of an SSBA

  • Transport of SSBAs between entities by authorised persons

  • Transport of SSBAs between facilities within an entity

  • Tier 1 versus Tier 2


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Transport Summary

  • Compliance with dangerous goods requirements

  • Transport security

  • Verification and Notification

  • Successful shipment

  • Transport by authorised persons

  • Tier 1 versus Tier 2


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Part 7Inactivation and Decontamination

  • It is not intended that all SSBAs are completely destroyed after use

  • Allows for agents to be used for further research following inactivation

  • Purpose is to ensure that the agent no longer qualifies as an SSBA, and that SSBAs cannot be accessed through an inadvertent release from waste products


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Inactivation and Decontamination (2)

  • Procedures

  • Waste Management

  • Record Keeping

  • Tier 1 versus Tier 2


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Part 8SSBA Management System Requirements

  • Establishment of systematic approach to the management of security of SSBAs

  • Systems

    • Develop, authorise and implement policy concerning management of SSBAs

    • Continual assessment and improvement of SSBA management systems

    • Communicate relevant information regarding SSBA management system and activities to personnel and other relevant parties


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Part 8SSBA ManagementSystem Requirements (2)

  • Policy

  • Roles, Responsibilities and Authorities

    • Top management

    • SSBA management committee

  • Checking and Corrective Action

    • Performance management and analysis of data

    • Records, documentation and data control

    • Internal inspection

    • Control of non-compliance and corrective action

    • Preventive action


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Tier 1 Versus Tier 2 SSBA Management System Requirements

  • Subclause 8.4.3 – Internal inspection

    • Internal inspections at planned intervals

      • Six monthly (Tier 1)

      • 12 monthly (Tier 2)


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SSBA Management System Requirements Summary

  • Establish and document policy

  • Top management

  • SSBA management committee

  • Checking and corrective action

  • Records, documentation and data control

  • Internal inspection

  • Control of non-compliance


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Part 9 Bibliography

  • Sets out the references and other standards

  • Normative references regarding other legislation


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Activity

  • Group 1

    • What information might be classed as sensitive information?

    • What are the requirements when sending SSBAs?

    • What policies and procedures do you already have in place that may be adapted to fit within the SSBA Regulatory Scheme?

  • Group 2

    • What records do you keep in relation to SSBAs?

    • What are the requirements when receiving SSBAs?

  • Group 3

    • How do you dispose of your records?

    • Identify who you think could fulfil the role of top management?


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Standards Review

  • General review

    • Feedback from implementation during 2009

    • Improve clarity

  • Amendments to the NHS Act

    • Suspected SSBAs

  • Consultation in August 2009


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Reporting Requirements and Timeframes


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Reporting

National Register

Data Collection

Overview of the Data Collection System

Reportable Event forms

Initial Registration

Incident Notification

Administrative Changes

Transfer In

Transfer Out

Destruction

Regular Report

Outline


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Reporting

  • The NHS Act stipulates that reportable events must be reported to the Secretary

  • These reports will be put on to the National Register


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National Register

  • Established by the NHS Act (s36)

  • Supported by mandatory reporting (s37 and s38)

  • Secure IT database

  • Record information on registered entities/facilities handling SSBAs

  • Users must update their handlings of SSBAs

  • Provision of information to intelligence and law enforcement agencies


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Data Collection

  • Initial registration is paper based and sent via registered post or courier

  • Notification of reportable events and annual/biannual reports can be submitted electronically via secure website or manually on paper

  • No access to National Register – good record keeping essential


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Reporting timeframes

  • Time frames for reporting set out in the NHS Regulations

  • The time frame depends on the type of reportable event and if the SSBA handled is Tier 1 or Tier 2

  • The time frames are:

    • Reporting events as they occur

    • Reporting events on discovery

    • Regular reporting (biannually or annually)


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Reporting timeframes (2)

  • Two types of reporting events as they occur

    • Reporting events as they occur – these reports are required within 2 business days of the event occurring

    • Reporting events after discovery - these reports are required within 2 business days of discovery of the event


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Reporting Eventsas they Occur

  • Handling a new SSBA

  • Handling for a purpose not already registered

  • Change of Responsible Officer or deputy details

  • Transfer of SSBAs

  • Disposal of entire holdings or resulting in less than the reportable quantity of toxins


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Reporting EventsOn Discovery of the Event

  • Loss

  • Theft/attempted theft

  • Unauthorised access/attempted unauthorised access

  • Accidental release

  • Infection with SSBA acquired from handling


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Reportable EventsRegular Reporting

  • These reports are required 6 monthly or 12 monthly and include:

    • Changes in registration details that are not required to be reported as they occur

  • Tier 1 agents: reports must be provided by 30 April and 31 October of each year

  • Tier 2 agents: reports must be provided by 30 April of each year


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Reporting Forms

  • Initial Registration

  • Incident Notification

  • Administrative Changes

  • Transfer In

  • Transfer Out

  • Destruction

  • Regular Report


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Initial Registration

  • Start to handle SSBA

  • Includes details of the:

    • Entity

    • Facility

    • Responsible Officer(s)

    • SSBA held and purpose

    • Declaration of compliance with Standards

  • Paper-based form (no on-line option)


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Incident Notification

  • Complete this form for the following situations:

    • Loss of SSBAs

    • Theft of SSBAs

    • Attempted theft of SSBAs

    • Unauthorised access to SSBAs or sensitive information relating to SSBAs

    • Attempted unauthorised access to SSBAs or sensitive information relating to SSBAs

    • Accidental release of SSBAs

    • Infection with SSBAs acquired from handling


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Administrative Changes

  • Complete this form for the following situations:

    • Start to handle a new SSBA

    • Recommence handling SSBA

    • Change purpose for handling an existing SSBA

    • Changes to Responsible Officer(s) details


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Transfer In

  • Complete this form if you have received an SSBA

  • Includes details of:

    • Sending facility

    • SSBA

    • Successful/unsuccessful transfer

    • What you intend to do with the SSBA


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Transfer Out

  • Complete this form if you have sent an SSBA

  • Includes details of:

    • Receiving facility

    • SSBA


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Destruction

  • Complete this form if you have destroyed your entire holding of an SSBA or destruction that has resulted in less than the reportable quantity of toxins


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Regular Report

  • This form will need to be completed ONLY if any of the Initial Registration details have changed (not including the details that are reported as they happen):

    • Entity details

    • Facility postal address or email

  • NB Change to facility physical address will require a new initial registration


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The Data Collection System

DCS

www.health.gov.au/ssba/dcs


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Reporting RequirementsSummary

  • Initial Registrations must use paper forms sent by registered post or courier

  • Paper forms and web based DCS

  • Reporting events as they occur

    • Within two days of the event occurring

    • Within two days of the discovery of the event

  • Regular reporting

  • Good record keeping is essential


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Inspection Process


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Monitoring and compliance

Inspectors

Commencement

Types of inspections

Outcomes

Inspector training

Outline


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Monitoring and Compliance

  • NHS Act s63–69

  • Inspections will be carried out on all regulated facilities

  • Inspections will evaluate compliance with:

    • NHS Act

    • NHS Regulations

    • SSBA Standards


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Inspectors

  • DoHA commissioned the Office of the Gene Technology Regulator (OGTR) to provide inspectors

  • In time, inspections for SSBA compliance may occur in the same visit as OGTR inspections


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Commencement

  • Inspections will commence in the first year of regulation

  • Tier 1 facilities will be inspected more frequently than Tier 2 facilities

  • Pattern for inspections and how frequently they will occur has not yet been determined


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Types of Inspections

  • Inspections may be:

    • Routine

    • Follow-up from routine

    • Review visits

    • Audits

    • Formal investigations

    • Unannounced ‘spot checks’


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Outcomes

  • Administrative

    • Communication and education activities

    • Provision of advice

    • Written remedial action

    • Written warnings

  • Legal

    • Notices issued under NHS Act

    • National authority disposal of SSBAs

    • Injunctions

    • Criminal prosecution


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Inspector Training

  • Inspectors from OGTR already have appropriate qualification in carrying out inspections

  • Inspectors will also receive special training in:

    • SSBA Regulatory Scheme

    • Suspicious behaviour

    • Quality management system assessment

  • Inspectors will be appointed by the Secretary


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SSBA Publications


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Guidelines

Fact Sheets

SSBA Newsletter

Security Risk Template

Outline


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SSBA Guidelines

  • Provide practical supporting information to assist with understanding how to achieve full compliance with:

    • The NHS Act

    • The NHS Regulations

    • The SSBA Standards


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Confirmatory Testing for SSBAs and Retention of Samples Sent for Testing

Entities and Facilities

Handling a Person or Animal, or Samples from a Person or Animal, Infected with an SSBA

Defining Loss, Theft and Accidental Release of SSBAs

Non-Registered Entities or Facilities

Reporting to the Department of Health and Ageing

Reporting to Law Enforcement and National Security Agencies

SSBA Toxins

SSBAs in the Natural Environment

The Transport Process

Guidelines


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Confirmatory Testing for SSBAs and Retention of Samples Sent for Testing

  • This guideline covers:

    • Reporting requirements

    • Handling of other samples following identification of an SSBA

    • Confirmatory testing


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Entities and Facilities

  • This guideline covers:

    • Defining an entity

    • Defining a facility

    • Leasing a facility from another entity


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Handling a Person or Animal, or Samples from a Person or Animal, Infected with an SSBA

  • This guideline covers:

    • Treatment of a person who is infected with an SSBA

    • Handling animals infected with an SSBA

    • Handling samples from infected persons or animals


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Defining Loss, Theft and Accidental Release of SSBAs

  • This guideline covers:

    • Legislation

    • Loss vs stolen

    • Accidental release


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Non-Registered Entities or Facilities

  • This Guideline covers:

    • Reporting requirements for non-registered facilities

    • Reporting flow chart


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Reporting to the Department of Health and Ageing

  • This guideline covers:

    • Reporting as events occur or on discovery of event

    • Regular reporting

    • Reporting timeframes

    • Process for reporting


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Reporting to Law Enforcement and National Security Agencies

  • This guideline covers:

    • Reporting to law enforcement and national security agencies

    • Incidents to report

    • Who to contact

    • When to contact agencies

    • Contact details

    • Information you may be asked to report


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SSBA Toxins

  • This guideline covers:

    • Handling toxins on the List of SSBAs

    • Reportable quantities for toxins on the List of SSBA

    • When to register for Tier 2 and/or Tier 1 if handling Clostridium botulinum


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SSBAs in the Natural Environment

  • This guideline covers:

    • SSBAs occurring in the natural environment

    • Inadvertent possession of an SSBA occurring naturally in the environment

    • Deliberate cultivation


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The Transport Process

  • This guideline covers:

    • Transport requirements for SSBAs

    • Sending SSBAs

    • Receiving SSBAs

    • Transport checklist


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Additional Guidelines

  • Prepared by the Australian Federal Police, including the Australian Chemical, Biological, Radiological and Nuclear Data Centre

    • Toxin Levels in Environmental and Clinical Samples

    • Indicators of Suspicious Behaviour in Laboratories Handling SSBA


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Fact Sheets

  • Overview

  • About Us

  • Legislative Framework

  • Exemptions

  • List of Biological Agents

  • Top Management


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Fact Sheets (2)

  • Monitoring and Compliance

  • National Health Security Act 2007 Amendments

  • Disposal

  • Domestic Legislation

  • International Conventions

  • Dual-use


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Security Risk Template

  • Aligns with the SSBA Standards

  • A tool for assessing compliance

    • Entities may use other tools

    • Use is not compulsory

  • The SRT is a checklist to use after completing a security risk assessment

  • SRT helps to ensure all risks have been identified and treated

  • Each section in the SRT covers areas within the SSBA Standards


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SSBA Newsletter

  • Stakeholder-oriented information

  • Raise awareness on the regulation of SSBA

  • Quarterly

  • Features include:

    • Key achievements and outcomes

    • Awareness raising issues

    • Upcoming events

    • Updates

    • Consultation advice and notices


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Copies of the SSBA Publications

Available through the Department of Health and Ageing web site:

www.health.gov.au/ssba


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Overall Summary

  • Setting the Scene

  • International Schemes

  • Technical Feasibility and Risk Report

  • Jurisdictional Context

  • National Health Security Act 2007

  • National Health Security Regulations 2008

  • SSBA Standards

  • Reporting Requirements and Timeframes

  • Inspection Process

  • SSBA Publications


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Stakeholder Training

  • December 2009

  • Training will cover:

    • SSBA Standards

    • Security risk templates

    • Reporting requirements and timeframes

    • National Register

    • Data Collection System

    • Suspicious behaviour

    • Compliance expectations

    • Guidelines


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Evaluation

  • Please complete the SSBA Road Show evaluation form provided


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Thank You

Further information on the SSBA Regulatory Scheme can be found at:

www.health.gov.au/ssba

[email protected]


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