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Evolution of the Mediation Field: Monthly Conversation Series with Field Leaders

Evolution of the Mediation Field: Monthly Conversation Series with Field Leaders
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L. Christine Lawson Litigation Attorney Womble Bond Dickinson Atlanta


Professional Biography:
Christine is an experienced product liability litigation and regulatory compliance attorney with more than 20 years of experience defending manufacturers and laboratories in complex cases in which medical and scientific facts were at issue. She focuses her practice on food and beverage regulation and litigation, as well as smoking and health litigation.
In her practice defending food product manufacturers, Christine relies on her first-hand experience as a small business owner of a company that makes snacks inspired by the dietary restrictions of her children on the autistic spectrum. Establishing this company has required her to navigate state and federal regulatory hurdles, giving her a client’s perspective on the compliance process and related disputes. Christine has earned the Food Defense Awareness Certification from the Food Safety Preventative Controls Alliance as well as the Better Process Control School Certification. She most recently co ....

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Do Not Take a Shot in the Dark: Important Considerations for Puerto Rico Employers Eyeing Mandatory COVID-19 Vaccination Programs | Littler


[co-author: José L. Maymí-González]
Multiple states and jurisdictions are reporting a deadly winter spike of COVID-19 infections. An excess of 220,000 cases of COVID-19 were reported in early December, a dramatic increase from the 44,783 reported in October. Nevertheless, a glint of hope flashes within the gloom of the COVID-19 pandemic: Operation Warp Speed, a partnership program between the public and private sectors to develop, produce, and mass distribute a COVID vaccine. Pfizer’s vaccine has a reported effectiveness rate of 82% after the first dose and a 95% rate after the second dose. This, and various other vaccines with similar effectivity rates, are currently in the race for government authorization for mass vaccinations, with Pfizer-BioNTech’s and Moderna’s vaccines having received Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA). This “emergency use” authorization stems from the FDA’s ability to greenlight unapproved ....

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