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AI for Health is a $60 million, five-year philanthropic program from Microsoft, created to empower nonprofits, researchers, and organizations tackling some of the toughest challenges in global health.
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AI for Health is a program focused on gathering and sharing data to speed up innovation and address difficult health issues. We seek to empower researchers around the world to have a greater impact on the people who need it most.
We partnered with Humanitarian OpenStreetMap Team (HOT) to improve the mapping of areas vulnerable to natural disaster and poverty, enabling communities to respond more quickly and effectively after disasters.
Many of our partners and projects invite volunteers to help their work across global social and environmental challenges. Learn about opportunities to participate in meaningful AI projects as a citizen scientist. Donate your computing time, label data, explore open data, identify images, and more.
The Good Food Guild is the only national trade association uniting food and drink crafters committed to environmentally sustainable and socially just production practices. With nearly 500 business members in over 45 states and Washington, D.C., the Guild is an economic force transforming the American food system.
The Good Food Merchants Alliance is a growing, national coalition of retailers who work in tandem to raise awareness of the role independent grocers play in maintaining a good food system and support the food crafters that make the shelves of exceptional grocers unique.
Pilot Flying J Pilot Flying J discount available at company-owned-and-operated Pilot or Flying J locations. Offer void where prohibited by law. Other terms and conditions may apply.
On March 15, 2023, the U.S. Environmental Protection Agency (EPA) issued its final Good Neighbor Plan, which secures significant reductions in ozone-forming emissions of nitrogen oxides (NOX) from power plants and industrial facilities. This action will save thousands of lives and result in cleaner air and better health for millions of people living in downwind communities.
The Environmental Protection Agency is taking final action to revise certain administrative deadlines under seven allowance trading programs for nitrogen oxides and sulfur dioxide, including all Cross-State Air Pollution Rule (CSAPR) trading programs and the Texas SO2 Trading Program. EPA proposed to revise these deadlines as part of the proposed Good Neighbor Plan published April 2022.
Think of the AQI as a yardstick that runs from 0 to 500. The higher the AQI value, the greater the level of air pollution and the greater the health concern. For example, an AQI value of 50 or below represents good air quality, while an AQI value over 300 represents hazardous air quality.
For each pollutant an AQI value of 100 generally corresponds to an ambient air concentration that equals the level of the short-term national ambient air quality standard for protection of public health. AQI values at or below 100 are generally thought of as satisfactory. When AQI values are above 100, air quality is unhealthy: at first for certain sensitive groups of people, then for everyone as AQI values get higher.
The AQI is divided into six categories. Each category corresponds to a different level of health concern. Each category also has a specific color. The color makes it easy for people to quickly determine whether air quality is reaching unhealthy levels in their communities.
Five major pollutantsEPA establishes an AQI for five major air pollutants regulated by the Clean Air Act. Each of these pollutants has a national air quality standard set by EPA to protect public health:
ENISA contributes to EU cyber policy, enhances the trustworthiness of ICT products, services and processes with cybersecurity certification schemes, cooperates with Member States and EU bodies, and helps Europe prepare for the cyber challenges of tomorrow.
The site is secure. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.
Cronobacter sakazakii is a bacteria commonly found in the environment. In most people it causes no symptoms but in some, particularly premature infants, infants under 2 months of age or infants with weakened immune systems fever, poor feeding, excessive crying or low energy as well as other serious symptoms can occur.
Consumers can request refunds for impacted products and find more information about Gerber Good Start by contacting the Gerber Parent Resource Center on behalf of Perrigo at 1-800-777-7690 anytime 24/7. Consumers with any health-related questions should contact their healthcare provider.
About PerrigoPerrigo Company plc is a leading provider of Consumer Self-Care Products and over-the-counter (OTC) health and wellness solutions that enhance individual well-being by empowering consumers to proactively prevent or treat conditions that can be self-managed. Visit Perrigo online at www.perrigo.com.
On November 1, 2022, Perrigo acquired Nestlé's Gateway Eau Claire, Wisconsin, plant, along with the U.S. and Canadian rights to the Good Start infant formula brand. Perrigo operates the Good Start infant formula brand in the United States and Canada while Nestlé operates the Good Start infant formula brand for Women Infants and Children (WIC) contracts.
Fashion for Good is a global initiative to inspire change and drive the collective movement to make fashion a force for good. We work directly with the fashion industry to innovate towards solutions that are better for people and the planet and empower behaviour change through our sustainable fashion Museum.
Host your most successful event ever with our new fundraising events and auctions software. Reach more supporters with an online or hybrid event and boost your return on investment with our simple, smart auction platform.
Stop paying for multiple tools and storing important donor data in spreadsheets or clunky databases. Use simple, smart fundraising software from Network for Good to get everything you need to raise money at your fingertips.
Use built-in communication tools to form connections with your donors through email, text messages, personal videos, and direct mail. Personalize your communications by pulling donor data directly from your database to segment supporters and create more effective messages.
Create beautiful, branded fundraising pages in minutes using our guided tool and expert recommendations. Plus, take advantage of our free data migration and onboarding support. Make fundraising less complicated with easy-to-use software and expert advice.
Share tasks and set reminders to improve collaboration among your team, volunteers, and board. Keep everyone on track and working toward your purpose with management tools that improve accountability and workflow.
This policy establishes the expectation that all NIH-funded investigators and staff who are involved in the conduct, oversight, or management of clinical trials should be trained in Good Clinical Practice (GCP), consistent with principles of the International Conference on Harmonisation (ICH) E6 (R2).1
The principles of GCP help assure the safety, integrity, and quality of clinical trials. GCP provides a standard for ensuring clinical trial compliance, implementation, data collection, monitoring, and reporting (e.g., safety data, accrual reports, study status, protocol deviations, unanticipated problems, or final data), and outline the responsibilities of Institutional Review Boards (IRBs), investigators, sponsors and monitors. GCP addresses elements related to the design, conduct and reporting (e.g., safety data, accrual reports, study status, protocol deviations, unanticipated problems, or final data) of clinical trials.
GCP principles constitute an international ethical and scientific quality standard for designing, conducting, recording, and reporting clinical trials. The principles were developed in 1996 by the ICH in collaboration with representatives from the European Union, Japan, and the United States. The U.S. Food and Drug Administration (FDA) requires GCP compliance for studies conducted under an investigational new drug application or investigational device exemption.
GCP describes the responsibilities of investigators, sponsors, monitors and IRBs in the conduct of clinical trials. Compliance with GCP provides assurance that the rights, safety and well-being of human subjects are protected, that clinical trials are conducted in accordance with approved plans with rigor and integrity, and that data derived from clinical trials are reliable.
This Policy applies to NIH-funded investigators and clinical trial site staff who are responsible for the conduct, management and oversight of NIH-funded clinical trials. 3 GCP training includes the Principles of ICH GCP found in Section 2 of ICH E6. 4 GCP training may be achieved through a class or course, academic training program, or certification from a recognized clinical research professional organization. Completion of GCP training will demonstrate that individuals have attained the fundamental knowledge of clinical trial quality standards for designing, conducting, recording and reporting trials that involve human research participants. GCP training should be refreshed at least every three years in order remain current with regulations, standards and guidelines. Recipients of GCP training are expected to retain documentation of their training.
Investigator: The individual responsible for the conduct of the clinical trial at a trial site. If a clinical trial is conducted by a team of individuals at a trial site, the investigator is the responsible leader of the team and may be called the principal investigator.
Clinical trial staff: Individuals, identified by the investigator, who are responsible for study coordination, data collection and data management. The central focus of clinical trial staff is to manage participant recruitment and enrollment, to maintain consistent study implementation, data management, and to ensure integrity and compliance with regulatory and reporting requirements. These individuals may also seek informed consent from prospective participants, enroll and meet with research participants, and collect and record information from research participants. Clinical trial staff may also be called the research coordinator, study coordinator, research nurse, study nurse or sub-investigator. 041b061a72