Occupational Health and Safety Act, 1993 (Act No. 85 of 1993)RegulationsHazardous Biological Agents Regulations1. Definitions |
In these Regulations any word or expression to which a meaning has been assigned in the Act shall have the meaning so assigned and, unless the context indicates otherwise -
"biological agent"
means any micro-organism, cell culture or human endoparasite, including any which have been genetically modified, which may cause an infection, allergy or toxicity, or otherwise create a hazard to human health;
"decontamination"
means to remove, as far as is reasonably practicable, all inanimate objects by way of sweeping, cleaning, washing, ventilating or any other process aimed at removing the contaminant;
"diagnostic laboratory"
means a workplace where diagnostic or other screening procedures are performed on blood or other potentially infectious materials;
"disinfect"
means to render non-viable virtually all recognised pathogenic micro-organisms, but not necessarily all microbial forms;
"engineering control measures"
means control measures that remove or reduce the exposure of persons at the workplace by means of engineering methods;
"Facilities Regulations’’
means the Facilities Regulations promulgated by Government Notice No. R. 2362 of 5 October 1990 under section 43 of the Act;
"General Administrative Regulations"
means the General Administrative Regulations promulgated by Government Notice No. R. 1449 of 6 September 1996 under section 43 of the Act;
"HBA"
means hazardous biological agents which are micro-organisms, including those that have been genetically modified, pathogens, cells, cell cultures and human endoparasites that have the potential to provoke an infection toxic effects, subdivided into the following groups -
a) | Group I HBA are HBA that is unlikely to cause human disease; |
b) | Group 2 HBA are HBA that may cause human disease and be a hazard to exposed persons, which is unlikely to spread to the community and for which effective prophylaxis and treatment is usually available; |
c) | Group 3 HBA are HBA that may cause severe human disease, which presents a serious hazard to exposed persons and which may present a risk of spreading to the community, but for which effective prophylaxis and treatment is available; |
d) | Group 4 HBA are HBA that causes severe human disease and is a serious hazard to exposed persons and which may present a high risk of spreading to the community, but for which no effective prophylaxis and treatment is available. |
"micro-organisms"
means microbiological entities, cellular or non-cellular, capable of replication or of transferring genetic material;
"monitoring"
means the planning and carrying out of the measurement programme and the recording of the results thereof;
"respiratory protective equipment"
means a device which is worn over at least the mouth and nose to prevent the inhalation of airborne hazardous biological agents, and which conforms to a standard, acceptable to the chief inspector:
"safety equipment"
means a contrivance or a device designed to as far as possible try and prevent injury;
"standard precautions"
means a synthesis of the major features of Universal Precautions (UP) and Body Substance Isolation (BSI) and applies to all persons coming into contact with potentially -infected persons, animals or animal products and potentially contaminated blood and other body fluids in health care facilities or elsewhere and -
a) | apply to – |
i) | all blood; |
ii) | all body fluids, secretions and excretions, except sweat, regardless of whether they contain visible blood or not; |
iii) | non-intact skin; |
iv) | mucous membranes: and |
v) | tissues; and |
b) | are designed to reduce the risk of transmission of HBA from both recognised and unrecognised sources of infection in workplaces; |
"The Act"
means the Occupational Health and Safety Act,1993 (Act No. 85 of 1993)