Compliance with Mobile Medical Devices Discussed in MedTech Intelligence
Device companies seeking to develop products that include a mobile app must ensure regulatory compliance with product and data safety.
Couch Authors Article on GLPs for Dietary Supplement Contract Labs
Supplement brands that partner with contract labs must ensure they are following good lab practices and other quality assurance programs.
Couch Co-Authors Article in FDLI Update on PMTAs for Deemed Products
In October the FDA Center for Tobacco Products (CTP) held a Public Meeting about Preparing Marketing Applications for Deemed Products. A summary of that meeting was co-prepared by Tara Lin Couch, Ph.D. and published FDLI Update magazine.
Steve Armstrong Interviewed on Marketing Claims
Consumers demand certain qualities—think clean label, zero sugar and non-GMO, for example, and marketing claims can affect the ways that foods and beverages are produced.
Dietary Supplement and FSMA EAS Webinar – On-Demand
Did you know that some parts of FSMA also apply to dietary supplements? Watch our EAS on-demand webinar to ensure your understanding with requirements.
FDA’s CTP Updates Industry on Premarket Tobacco Product Applications for Deemed Products
If you missed FDA’s public meeting on PTMAs, click here for a summary co-prepared by EAS and published in the Food Drug Law Institute Update magazine.