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How to Approach Embodied Carbon Reduction within an Architectural Project

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In order to start integrating embodied carbon studies into projects to meet sustainability goals, it is important to consider many factors such as carbon (kgCO2e) values, and what typical ranges of values to be aware of when designing for embodied carbon reduction. This e-book presents an overview of how to start integrating embodied carbon studies in your projects.
Why Calculate Embodied Carbon in the Early Stages of a Project?
Annually, the embodied carbon of building structure, substructure, and enclosures are responsible for 11% of global GHG emissions and 28% of global building sector emissions. Between 39%-80% of a building’s total Carbon Footprint is a result of the embodied carbon from building materials. If evaluated early in the design phase, 80% of a building’s embodied carbon can be reduced. ....

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Dulux's commitment to a sustainable future | Architecture & Design

Dulux meets the challenge of a sustainable future by staying at the forefront of technology and investing in research and development to create innovative, high performance products with reduced environmental impact.
Dulux’s innovations in sustainable solutions are an outcome of their proactive shift from solvent-based products to water-based alternatives, and the introduction of Australia s first low VOC paint in the early 1990s among others.
From initiating sustainable business partnerships, through to product innovations and right up to the actual clean-up stage including waste paint disposal, Dulux continues to develop new ways to reduce the environmental impact of their products, without affecting their outstanding performance and the quality results that Australia s professional and DIY painters have come to expect from the brand. ....

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TGA Removes Some China Made Face Masks From the Therapeutic Goods Register

TGA Removes Some China Made Face Masks From the Therapeutic Goods Register
The Therapeutic Goods Administration (TGA) has said that not all face masks meet the necessary regulatory requirements for safe use and may remove some masks from the Australian Register of Therapeutic Goods (ARTG) following a post-market review.
The Australian sponsors of 5 out of 15 Chinese-made face mask products have been advised to issue either a product defect alert or product notification that describes the nature of the concern to their customers, “so that customers can consider the setting the face mask is being used in, so as to minimise risks associated with its continued use.” ....

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FDA warns vs. purchase, use of AiDeLai face masks

January 15, 2021 | 7:20 pm
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The Food and Drug and Administration (FDA) has warned the public not to use two face mask brands which did not go through the proper authorization process.
In an advisory released on Friday, FDA Director-General Rolando Enrique D. Domingo said a brandless product referred to as “Disposable Face Mask” and the AiDeLai Face Mask have not been certified by the agency.
Republic Act No. 9711 or the FDA Act of 2009 prohibits the manufacture, importation, exportation, sale, offering for sale, distribution, transfer, non-consumer use, promotion, advertising, or sponsorship of any health product without the agency’s evaluation. ....

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FDA warns against Toni Gonzaga's cologne brand | Philippines Lifestyle News

January 12, 2021
The Food and Drug Administration (FDA) warns against the purchase and use of cologne spray sold by the company of actress Toni Gonzaga and vlogger Winnie Wong.
According to the FDA, through post-marketing surveillance, POUF! Everyday Bloom Cologne Spray was found to have no valid Certificate of Product Notification.
Because of this, the agency said they were unsure of the quality and safety of its use.
They said it is possible that the said product will cause health risks to consumers.
“The abovementioned product was verified by FDA through postmarketing surveillance and shows no valid Certificate of Product Notification (CPN) as of 17 December 2020. Pursuant to Book II, Article I, Section 1 (a) of the Rules and Regulations Implementing Republic Act No. 9711, otherwise known as the “Food and Drug Administration Act of 2009”, the manufacture, importation, exportation, sale, offering for sale, distribution, transfer, non-consumer use, promo ....

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