Pira 2009 Sept. Arlington Taiwan New Chemical Regulation2
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The document summarizes Taiwan's new chemicals control regulation which aims to construct a Taiwan Existing Chemicals List and establish procedures for new chemicals notification and nomination. It outlines key details of the new regulation including nomination of existing chemicals by July 2010, building of the chemicals list by July 2011, and new chemicals notification requirements starting July 2011. Manufacturers and importers are advised to start preparing now by nominating their existing chemical substances and finding local contacts in Taiwan.
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3) Different categories of drugs and their registration processes, timelines, and requirements. Priority review is given to drugs addressing public health issues.
4) Ongoing efforts to strengthen regulatory capacity, encourage compliance, and facilitate access through various initiatives and
ICH guidelines
This document provides an overview of ICH guidelines related to quality (Q series). It describes the composition and objectives of ICH, which aims to harmonize technical requirements for pharmaceutical registration among regulators and industry in the EU, Japan, and US. The key points are that ICH guidelines are divided into four categories, including the Q series which relates to chemical and pharmaceutical quality. The Q series guidelines cover topics like stability testing, analytical validation, impurities, and residual solvents. The goal is to establish common standards for assessing safety, quality and efficacy of medicines.
Drug Control and Registration in Thailand - 2010
The document discusses Thailand's drug control and registration system. It provides details on the organization and responsibilities of key agencies like the Ministry of Public Health and Food and Drug Administration. It also summarizes Thailand's drug licensing process, registration system for new and generic drugs, safety monitoring programs, and efforts to harmonize standards with ASEAN countries. The document aims to provide an overview of Thailand's regulatory framework and approval processes for drugs.
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Mohammad Nur Sharif presented on impurities in drug substances. The objectives were to make recommendations to applicants on reporting, identifying, qualifying, and providing source information on impurities in new drug substances. Impurities can come from raw materials, reagents, manufacturing processes, atmospheric contamination, defects in processes, and intermediate products. Thresholds for reporting, identifying, and qualifying impurities were provided based on maximum daily dose.
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This material safety data sheet provides information on ecoClean Concentrate, a general purpose cleaner. It contains plant-based fatty acids, amino acids, corn oil, and other naturally derived and non-hazardous ingredients. No ingredients are considered carcinogenic or toxic. The product is classified as non-hazardous and poses no known health risks if used as intended. Proper handling and storage procedures are outlined.
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This presentation provides an overview of TSCA as it is currently configured and also reviews plans to reform the bills and possible implications on businesses.
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2) Approval timelines for new drug registration range from 6-24 months depending on the country. Singapore and Thailand typically approve within 6-12 months while Indonesia, Philippines, and Malaysia may take 12-24 months.
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Safer chemicals within REACH
The document summarizes the REACH regulation which aims to improve the protection of human health and the environment from risks posed by chemicals. It requires companies to gather information on the properties of their chemical substances, register the information in a central database, and downstream users can access the information. Chemicals that pose very high concern require special authorization for use, with the goal of promoting substitution of hazardous chemicals with safer alternatives over time through this process.
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Aluminium Oxide Chromatography MSDS including the physical and chemical properties, composition also information on ingredients which allows you to analyze the product.
Therapeutics goods administration & Row Countries
The document discusses regulatory requirements for pharmaceutical products in Australia and other countries collectively referred to as the "Rest of the World" or ROW. It outlines the role of the Therapeutic Goods Administration (TGA) in Australia to ensure quality, safety and efficacy of medicines. The TGA approves higher risk medicines and includes lower risk listed medicines in the Australian Register of Therapeutic Goods. Manufacturers must be licensed and comply with Good Manufacturing Practice standards. ROW countries have similar regulatory frameworks with a focus on pre-market assessment, post-market monitoring, and licensing of manufacturers. Requirements for registration in various ROW regions are also summarized.
About TURA
The Massachusetts Toxics Use Reduction Act of 1989 was the first state law to require reducing the use of toxic chemicals. The law achieved significant reductions in the use and releases of carcinogens and other toxics. Specifically, use of carcinogens decreased by 31% and byproducts from carcinogens decreased by 49% between 1990 and 2005. The Toxics Use Reduction Institute provided technical assistance and evaluated alternatives to help industries implement less toxic processes. The program's costs were outweighed by estimated economic and health benefits, demonstrating that reducing toxin use can improve both environmental quality and business competitiveness.
Key Points of Toxic Substances Control Act and Safe Cosmetics Act
The document summarizes a webinar on green business and chemical policy reform. It discusses the mission of the Green Business Network to promote a green economy. It outlines Green America's programs and membership opportunities for businesses. Experts from the American Sustainable Business Council and Campaign for Safe Cosmetics discuss the need to reform chemical policy and laws, noting the ubiquity of chemicals and lack of safety data. They argue reform would create a level playing field and expand markets for safer products.
MSDS CosmoMix-ACE
Material Safety Data Sheet (MSDS) for CosmoMix-ACE. Powderized saturated lipid formulation manufactured by Encapsula NanoSciences that is used specifically in the cosmetic industry. The brand name is CosmoMix-ACE. The CosmoMix-ACE formulation is composed of saturated phospholipids.
Similar to Pira 2009 Sept. Arlington Taiwan New Chemical Regulation2 (20)
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Find Latest India News and Breaking News these days from India on Politics, Business, Entertainment, Technology, Sports, Lifestyle and Coronavirus News in India and the world over that you can't miss. For real time update Visit our social media handle. Read First India NewsPaper in your morning replace. Visit First India.
CLICK:- https://firstindia.co.in/
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Find Latest India News and Breaking News these days from India on Politics, Business, Entertainment, Technology, Sports, Lifestyle and Coronavirus News in India and the world over that you can't miss. For real time update Visit our social media handle. Read First India NewsPaper in your morning replace. Visit First India.
CLICK:- https://firstindia.co.in/
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