Packaging and Paper Products definition

Packaging and Paper Products or “PPP” means those packaging and paper products that are more thoroughly described in the Environmental Management Act, Schedule 5 of the Regulation, and the approved Stewardship Program Plan;;

Examples of Packaging and Paper Products in a sentence

  • We wanted to further provide our input and feedback to be included in the report, from the perspective of an existing hauler operating in the sector and industry.During the forum discussions, it was suggested that EPR for Packaging and Paper Products be expanded into the ICI sector.

  • King County, Department of Natural Resources and Parks, Seattle Public Utilities, “Container Deposit Study: Phase III: Costs and benefits of Residential Packaging and Paper Products in Washington State” November 2020 Eunomia Research & Consulting Inc.

  • In May 2011, the Province amended the Recycling Regulation to include a new category: Packaging and Paper Products (PPP).

  • The study found that three main sub-sectors contribute to 82% of all Packaging and Paper Products (PPP) disposed (Table 8).

  • Transition of Operational and Financial Responsibility of Blue Box Program to Producers of Packaging and Paper Products As noted, the letter requires producers of packaging, which is managed in the Blue Box Program, to take over operational and financial responsibility of the program over the period of January 1, 2023 through January 1, 2025.

  • In 2014, a private sector industry stewardship organization MMBC (now RecycleBC) assumed responsibility for recycling Packaging and Paper Products from single family and multi-family homes, as legislated by the Province.

  • Product Stewardship Institute, Summary of Elements of Packaging and Paper Products (PPP) EPR Legislation (2020), https://cdn.ymaws.

  • Extended Producer Responsibility for Packaging and Paper Products: policies, practices, and performance.

  • Packaging and Paper Products Stewardship Act● Illinois Statewide Recycling Needs Assessment Advisory Council established.

  • Recalling its earlier discussions on this subject, the Bureau may provide guidance to the ITC for its preparation of proposals to be transmitted to the Executive Committee of the UNECE (E/ECE/1434/Rev.1, paragraph 36).

Related to Packaging and Paper Products

  • Packaging means the assembly of components necessary to ensure compliance with the packaging requirements of these regulations. It may consist of one or more receptacles, absorbent materials, spacing structures, thermal insulation, radiation shielding, and devices for cooling or absorbing mechanical shocks. The vehicle, tie-down system, and auxiliary equipment may be designated as part of the packaging.

  • Packaging Materials means the packaging materials for any of the Products, including product labels, packaging inserts, external packaging and similar materials.

  • Tobacco products means cigars, cigarettes, cheroots, stogies, periques, granulated, plug cut, crimp cut, ready rubbed, and other smoking tobacco, snuff, snuff flour, moist snuff, cavendish, ping and twist tobacco, fine-cut and other chewing tobaccos, shorts, refuse scraps, clippings, cuttings and sweepings of tobacco, and other kinds and forms of tobacco, prepared in such manner as to be suitable for chewing or smoking in a pipe or otherwise, or both for chewing and smoking.

  • Consumables and medical devices means (consumables) items that require regular replacement (e.g. batteries) to keep a medical device (such as a hearing aid) operational. Many medical devices require consumables.

  • NEC Electronics products means any product developed or manufactured by or for NEC Electronics (as defined above).

  • Specialty drug means a prescription drug that:

  • API means American Petroleum Institute.

  • Radiopharmaceutical quality assurance means, but is not limited to, the performance of appropriate chemical, biological, and physical tests on potential radiopharmaceuticals and the interpretation of the resulting data to determine their suitability for use in humans and animals, including internal test assessment, authentication of product history, and the keeping of proper records.

  • Manufacturing means all activities related to the manufacture of a Compound, including planning, purchasing, manufacture, processing, compounding, storage, filling, packaging, waste disposal, labeling, leafleting, testing, quality assurance, sample retention, stability testing, release, dispatch and supply, as applicable.

  • Specialty Drugs means drugs listed on the Approved Drug List meeting certain criteria, such as:

  • FCA : means the Financial Conduct Authority.

  • Marijuana products means concentrated marijuana products and marijuana products that are comprised of marijuana and other ingredients and are intended for use or consumption, such as, but not limited to, edible products, ointments, and tinctures.

  • Tobacco product manufacturer means an entity that after the date of enactment of this Act directly (and not exclusively through any affiliate):

  • Manufacturing Facility means buildings and structures, including machinery and equipment, the primary purpose of which is or will be the manufacture of tangible goods or materials or the processing of such goods or materials by physical or chemical change.

  • Remanufacturing means the activity of overhauling, retrofitting, fabricating, or repairing a product or its component parts for ultimate sale at retail.

  • Aerosol coating product means a pressurized coating product containing pigments or resins that dispenses product ingredients by means of a propellant, and is packaged in a disposable can for hand-held application, or for use in specialized equipment for ground traffic/marking applications.

  • Specialty coating means any coating that is manufactured and used for one (1) of the following specialized applications:

  • Distillery manufacturing license means a license issued in accordance with

  • Pharmaceutical care means the provision of drug therapy and

  • Manufacturing Materials means parts, tools, dies, jigs, fixtures, plans, drawings, and information produced or acquired, or rights acquired, specifically to fulfill obligations set forth herein.

  • veterinary surgeon means a veterinary surgeon within the meaning of the Veterinary Surgeons Act 1936.

  • Labeler means an entity or person that receives prescription

  • Pharmaceutical Product shall have the meaning ascribed to such term in Section 3.1(hh).

  • Steel Products means products rolled, formed, shaped, drawn, extruded, forged, cast, fabricated or otherwise similarly processed, or processed by a combination of two or more or such operations, from steel made by the open heath, basic oxygen, electric furnace, Bessemer or other steel making process.

  • Marketing Materials has the meaning ascribed thereto in NI 41-101;

  • Drug Substance means an active ingredient that is intended to furnish pharmacological activity or other direct effect in the diagnosis, cure, mitigation, treatment, or prevention of disease or to affect the structure or any function of the human body, but does not include intermediates used in the synthesis of such ingredient.