The Food and Drug Administration (FDA) has issued its “Strategic Plan for
Regulatory Science,” a document deemed to be the agency’s “blueprint for
overhauling the science it uses to develop and evaluate food, medicines, and
medical devices.” In a section underscoring the agency’s emphasis on food
safety, the document focuses on prevention and risk-based priorities required
by the Food Safety Modernization Act.

“To effectively implement this new food safety mandate, it is imperative that FDA ensures a strong science infrastructure, clearly identifies its research needs, and collaborates with other public health and research agencies in the [f]ederal government, state government agencies, academia, and private industry,” states the document, which details FDA’s Regulatory Science Initiative outlined in October 2010.

Regarding food science, FDA plans to (i) “[e]stablish and implement centralized planning and performance measurement processes,” (ii) “[i]mprove information sharing internally and externally,” (iii) “[m]aintain mission critical science capabilities,” and (iv) “[c]ultivate expert institutional knowledge.” The agency intends to involve stakeholders from the private sector in accomplishing its plan.

About The Author

For decades, manufacturers, distributors and retailers at every link in the food chain have come to Shook, Hardy & Bacon to partner with a legal team that understands the issues they face in today's evolving food production industry. Shook attorneys work with some of the world's largest food, beverage and agribusiness companies to establish preventative measures, conduct internal audits, develop public relations strategies, and advance tort reform initiatives.

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