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From our experience in multiple industries and consultation with regulatory experts, Ampacet has developed a new portfolio of medical grade masterbatch solutions. Our extensive testing program helps customers meet all performance criteria and compliance with the increasingly stringent requirements of regulatory agencies. For more information about Ampacet medical grade masterbatches and complete Regulatory Status, please complete the product ...
ByAmpacet Corporation based in Tarrytown, NEW YORK (USA)
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Today’s food and beverages (F&B) are much more than just simple "organic fuels" needed for survival. Beyond their nutritive value, they are consumed for their taste or flavor. Increasingly, they are also a source for maintaining health and enhancing our well-being via high-quality nutrition. At the same time, with an ever-increasing number of processed foods, food quality and safety aspects are becoming more important. All the more because foods are highly complex materials – prone to degradation ...
ByMetrohm AG based in Herisau, SWITZERLAND
Our comprehensive training package provides a regulatory overview of OSHA, information on the new labeling requirements, as well as the new SDS ...
ByComprehensive Safety Compliance, Inc. (CSC) based in Pittsburgh, PENNSYLVANIA (USA)
Governments and public bodies are often leaders in environmental and safety performance. Nimonik helps them streamline their tools and ensure they are compliant across their ...
ByNimonik Inc based in Montreal, QUEBEC (CANADA)
dataEssence software is ideal for managing complex ingredients such as essential and fragrance oils, and simplifying the process of blending those ingredients for multiple ...
ByData Essence Limited based in London, UNITED KINGDOM
dataEssence software offers a compliance solution for the fragrance industry to efficiently manage regulatory affairs including generating SDS reports, CLP labels and IFRA ...
ByData Essence Limited based in London, UNITED KINGDOM
In order to bring new treatments to patients, we conduct clinical trials to assess the safety and efficacy of our investigational medicines. This information is submitted to regulatory agencies, such as the U.S. Food and Drug Administration (FDA), the European Medicines Agency, and Health Canada, to enable approval for patient use. ...
ByZymeworks Inc based in Vancouver, BRITISH COLUMBIA (CANADA)