Preface This is the first edition of CAN/CGSB/CSA-Z1640, Personal protective equipment (PPE) for investigating and dismantling clandestine drug laboratories. The objective for this Standard is to assist first responders and other agencies in selecting the appropriate level and type of personal protective equipment (PPE) when investigating and dismantling clandestine synthetic drug laboratories (CDLs) and marijuana grow operations (MGOs). The PPE selection guidance in this Standard takes a risk-based approach in which selection of the appropriate level of protection is based on the identification and assessment of suspected and known hazards and risks during the various operations of the investigation and dismantling process. It is intended to ensure that all responders are provided with a consistent level of protection, regardless of responder service or jurisdiction. The requirements and guidance provided in this Standard result from consensus of the CSA-CGSB Technical Committee on Personal Protective Equipment for Clandestine Drug Laboratories, which represents a broad spectrum of stakeholder interests. The Technical Committee received input from other stakeholders during the development of this Standard and through public comments received as a result of a wide distribution of the draft Standard during the CSA Public Review and Comment period. The Technical Committee acknowledges that information with respect to hazards and risks associated with CDL and MGO operations is ever evolving and that periodic revisions to the Standard will be necessary to incorporate new information that becomes available.
Scope 1.1 This Standard provides requirements and guidance to assist first responders and other agencies in selecting the appropriate level and type of personal protective equipment (PPE) when investigating and dismantling clandestine synthetic drug laboratories (CDLs) and marijuana grow operations (MGOs) so as to reduce personal risk in the execution of their responsibilities. 1.2 This Standard takes a risk assessment approach in providing recommendations for whole-body protection (respiratory and dermal) to protect against anticipated and known hazards and risks associated with CDL and MGO operations. To facilitate PPE selection, this Standard provides information on the elements of an illicit drug response operation and hazards and risks associated with CDLs and MGOs. This Standard addresses integration with other PPE and provides guidance on limitations of PPE. 1.3 This Standard does not address operational or tactical procedures for responding to a CDL or MGO, except where they have a direct impact on the selection of PPE. This Standard does not provide information on sampling procedures or analytical methods for illicit drugs and associated chemicals. This Standard does not address the remediation phase of a CDL or MGO; however, the guidance provided in this Standard may be used by agencies involved in remediation activities. Clandestine explosive laboratories can be mistaken for a CDL since common chemicals can be found in both. Synthetic drug labs and homemade explosive labs have similar characteristics and dangerous conditions as they share common precursors and processes. Certain explosives can be mistaken for drugs, specifically hydrogen peroxide-based explosives triacetone triperoxide (TATP) and hexamethylene triperoxide diamine (HMTD), which are crystalline, odourless, shock sensitive powders similar in appearance to a synthetic drug.
1.4 Within the Canadian legislative framework, a variety of regulations apply to the first responders, depending on the jurisdiction. These shall be taken into consideration when using this Standard. 1.5 In this Standard, "shall" is used to express a requirement, i.e., a provision that the user is obliged to satisfy in order to comply with the Standard; "should" is used to express a recommendation or that which is advised but not required; and "may" is used to express an option or that which is permissible within the limits of the Standard. Notes accompanying clauses do not include requirements or alternative requirements; the purpose of a note accompanying a clause is to separate from the text explanatory or informative material. Notes to tables and figures are considered part of the table or figure and may be written as requirements. Annexes are designated normative (mandatory) or informative (non-mandatory) to define their application.
GST REG No R119441681
QST REG No R1006017360