Safety Information. Any other bulletins may only be posted by mutual agreement between the Union and designated Management.
Safety Information. All chemicals, equipment, and materials proposed or used in the performance of this Contract shall conform to the requirements of the Occupational Safety and Health Act of 1970. Vendor shall furnish all material safety data sheets for any regulated chemicals, equipment, or hazardous material at the time of delivery.
Safety Information. All chemicals, equipment and materials proposed and/or used in the performance of this purchase order must conform to the standards required by the Occupational Safety and Health Act of 1970. Bidders must furnish Safety Data Sheets (SDS) for any regulated chemicals, equipment or hazardous materials at the time of delivery.
Safety Information. The Health and Safety Committee shall be provided with all accident reports and shall have full access to safety information known to the Employer regarding potentially hazardous substances utilized in the workplace.
Safety Information. The Employer shall annually utilize a portion of one of the initial planning days to review with unit member's key sections of this Agreement, administrative bulletins, and laws, which pertain to safety/discipline.
Safety Information. The safeguarding of human subjects participating in clinical trials and patients who use devices or take investigational or licensed medicinal products, certain consumer healthcare products, vaccines, or biological products (the foregoing collectively referred to as the “Products”) is of paramount importance. Products would also include blinded, placebo, or control agents used in clinical studies. Therefore, the Parties require a framework for management of Human Safety Information. The framework includes, but is not limited to: · Safety reviews of Products to evaluate emergent safety data · Creation of appropriate committees and safety departments to proactively address human safety throughout Product development · Reporting of Human Safety Information to safety departments in a timely fashion. This includes any information relating to human health and/or wellbeing arising following exposure of humans to products including reports of drug abuse or overdose, reports of drug interaction, or information received as part of product complaints · Animals should be used in research only when required by regulatory authorities or where there are no alternatives through adherence to the “3R” Principles—reducing the Confidential treatment has been requested with respect to portions of this agreement as indicated by “[***]” and such confidential portions have been deleted and filed separately with the Securities and Exchange Commission pursuant to Rule 24b-2 of the Securities Exchange Act of 1934, as amended. number of animals used, replacing animals with non-animal methods whenever possible and refining the research techniques used. In addition, the Parties include two more R’s: Responsibility and Respect for animals involved in animal research. · The Parties believe in using the highest standards for the humane care and treatment of all animals used in research, development and testing, including adherence to the principles (listed below), and all applicable legal and regulatory requirements, with a default to which ever is more stringent. · Access to species appropriate food and water · Access to species specific housing, including species appropriate temperature and humidity levels · Access to humane care and a program of veterinary care · Animal housing that minimizes the development of abnormal behaviors and allows for normal species specific behavior, · Adherence to principles of replacement, reduction and refinement in the design of in vivo studies · Study d...
Safety Information. For the safety of yourself and others, and to avoid damage to equipment and vehicles, all personnel handling the equipment must read the safety precautions mentioned in the manual.
Safety Information. If at any time during the Term, each Party becomes aware of any information concerning any safety issues, adverse experiences, or any product complaints associated with adverse experiences related to any Licensed Compound or Licensed Product, such Party shall promptly provide such information to the other Party.
Safety Information. Prior to the Transfer Date, Prothena shall have the right to report all safety information to Regulatory Authorities with respect to the Licensed Program Antibodies and/or Licensed Program Products in the Territory hereunder, and shall promptly provide Celgene with all information concerning the pharmaceutical safety of Licensed Program Antibodies and/or Licensed Program Products in the Territory. After the Transfer Date, Celgene shall have the right to report all safety information to Regulatory Authorities with respect to the Licensed Program Antibodies and/or Licensed Program Products in the Territory hereunder, and shall promptly provide Prothena with all such information concerning the pharmaceutical safety of Licensed Program Antibodies and/or Licensed Program Products in the Territory.
Safety Information. While participating in events held or sponsored by the Texas Association Family, Career and Community Leaders of America (Texas FCCLA) “social distancing” must be practiced and face coverings worn at all times (exceptions listed above) to reduce the risks of exposure to COVID-
