Cosmetics each member is permitted to wear cosmetics of conservative color and amount.
Cosmetics. Supplier shall comply with the requirements specified in 923-2001-XX “WWOPS: Global Cosmetics Quality and Workmanship Standards.”
Cosmetics. 2.2 For bilateral cooperation related to inspection and quarantine in the area of imported and exported foodstuffs and cosmetics, Chapter 6 (Technical Barriers to Trade), Chapter 7 (Sanitary and Phytosanitary Measures) of the Free Trade Agreement between the Swiss Confederation and the People’s Republic of China signed on 6 July 2013 and other relevant agreements between the Parties or their authorities apply.
Cosmetics. In addition to means and areas of cooperation set out in Article 4 of the Agreement, the Parties will in the area of cosmetics in particular cooperate on the following:
Cosmetics. Supplier shall comply with the requirements specified in Dot Hill's Global Cosmetics—Quality—Workmanship specifications.
Cosmetics. Based upon the results of the initial medical assessment, Provider will administer Botox injections upon request by the Client.
Cosmetics. Members of a European Parliament committee have approved a resolution that aims to establish a global ban on animal testing for cosmetics by 2023. The resolution calls on the Commission, Council and Member States to push for such a ban when meeting with institutions from other countries, regions and the UN. REACH How to avoid unnecessary testing on animals Under REACH, testing on vertebrate animals (e.g. rats, other mammals or fish) can only be used as a last resort to fulfill information requirements for registration. For companies manufacturing or importing between 1 to 100 tons per year, there are multiple ways to avoid unnecessary animal testing and to reduce the number of animal tests. For each individual information requirement you should consider the following:
Cosmetics. Male Cadet are not authorized to wear cosmetics. Female Cadet may wear cosmetics; however, if worn, they will be conservative (moderate, being within reasonable limits; not excessive or extreme) and in good taste. Female Cadet will not wear shades of lipstick that detract from the uniform, or that are extreme colors. Some examples of extreme colors include but are not limited to, purple, gold, blue, black, bright (fire-engine) red, and fluorescent colors. Cosmetics will not be worn during field conditions.
Cosmetics. May be used at minimal levels and must adhere to standards of professional appearance and taste.
Cosmetics. The claim on a cosmetic product that in Ayurvedic medicine, a botanical in the formula has been traditionally used for its anti-oxidant effects. A fragrance developed from a flower native to the Democratic Republic of the Congo, where the odor compounds have been acquired using headspace technology. What Your Company Should Do If the Nagoya Protocol Applies Approaches to compliance diverge significantly depending on the area of activity and the degree of reliance on biological materials. From the perspective of EU enforcement authorities, the following is typically expected: Standard operating policies laying out the company’s process of verifying the existence of and compliance with access and benefit-sharing rules. For a large company, this may consist of multiple SOPs to handle different stages of the product development process (e.g., obtaining biological material, collaboration with third parties, patent filing and commercialization). Internal measures to communicate the implementation of the Nagoya policy to relevant employees and to provide appropriate training. Appointment of a contact person who has the appropriate background to deal with Nagoya compliance. This individual should also have sufficient resources to implement the Nagoya policy. An internal system to track and trace when biological materials enter the company, how they are used, and when they leave the company. This often requires a sophisticated IT platform, given the large amount of data involved. The process should at least be able to document the following information on biological materials: (i) the date and place of obtaining the material, (ii) a description of the material and its source, (iii) previous holders of the material, (iv) the presence or absence of obligations relating to access and/or benefit-sharing, and (v) whether these obligations have been complied with according to the standards set out in the compliance policy. Organizing such a system requires significant investment of time and resources, as well as senior management buy-in. Although legal or IP typically leads the process, the cross- functional involvement of regulatory, procurement, commercial and R&D is often essential. As an alternative to a fully-fledged, top-down compliance program, some companies have opted to build their process (and experience) through pilot projects. They would select one or a few key products, e.g., in terms of profitability and risk exposure, and check whether provi...
