It’s here! FDA creates Office of Dietary Supplement Programs

Elevating the program’s position will raise the profile of dietary supplements within the agency, and will enhance the effectiveness of dietary supplement regulation by allowing ODSP to better compete for government resources and capabilities to regulate this rapidly expanding industry, said the Agency in a statement.

The dietary supplement program was established 20 years ago, during which time the industry has grown from about $6 billion to more than $35 billion in annual sales.

Industry welcome​

The five trade associations representing the dietary supplement industry were quick to welcome the elevation of the Division of Dietary Supplement Programs (DDSP) to an “Office” status.

A statement from the American Herbal Products Association (AHPA), the Consumer Healthcare Products Association (CHPA), the Council for Responsible Nutrition (CRN), the Natural Products Association (NPA), and the United Natural Products Alliance (UNPA) read: “There has been considerable industry growth since DDSP was established in 1994, and with this growth, new regulatory challenges within the industry have presented themselves. ​

“The five associations have been consistent and longstanding in their joining together to urge FDA to take stronger enforcement action against companies illegally manufacturing and selling adulterated products. In a letter of support to Congress sent earlier this month, the associations expressed belief that the elevation of DDSP to an ‘Office’ could help ‘increase FDA’s abilities to take more aggressive enforcement action.’ Additionally, the groups anticipate that the elevation could ‘raise the visibility and attention for dietary supplement safety and compliance measures at FDA,’ as well as ‘better utilize CFSAN’s enforcement resources.’”​

“Overall, the industry views the elevation of DDSP not only as a demonstration of the government’s commitment to eliminating the illegal activity and leveling the playing field for the responsible companies already following the law, but also as an important step for increasing consumer safety by cracking down on rogue manufacturers who sell illegal products. As stated in an earlier joint letter to HHS, ‘Such a move would aid in accomplishing FDA’s current and long-range goals related to dietary supplements’.”​

'Long overdue'​

Dan Fabricant, PhD, Executive Director and CEO of NPA, said: “This is a long overdue step towards elevating the dietary supplement division within FDA so that it can exercise all the authorities it has to regulate this important industry.​

“America’s dietary supplement supply is the safest in the world and this will give consumers additional confidence that the natural products they prefer meet their expectations. We strongly support this decision and will continue to work with FDA and other regulatory officials to deliver quality products for the millions of people in the US and around the world.”​

Leadership​

The new permanent leadership of the ODSP is still being identified, but Bob Durkin will continue to serve as Acting Office Director in the meantime.

As a result of the transition announced today, ODSP’s former parent office will now be known as the Office of Nutrition and Food Labeling, under the leadership of Doug Balentine, PhD, who joined FDA on December 14, 2015.

Dr Balentine has a PhD in food science and nutrition from Rutgers University. As the head of the Office of Nutrition and Food Labeling, Dr Balentine will oversee the development of policy and regulations for nutrition labeling and food standards, infant formula and medical foods Dr. Balentine brings a wealth of knowledge and expertise to this position.

Ramping up enforcement​

The Agency noted that it has taken numerous actions on dietary supplements to protect public health in the last several years, and the ODSP will continue to utilize its current authorities and available resources to monitor the safety of dietary supplement products by continuing to:

Take action to remove from the market supplement products that are dangerous to consumers;

Work with FDA’s Center for Drug Evaluation and Research to help remove from the market products falsely labeled as dietary supplements that contain potentially harmful pharmaceutical agents;

Enforce the dietary supplement good manufacturing practices (GMP) regulation, giving priority to cases in which GMP violations:

Potentially compromise product safety;

Fail to ensure product identity, potentially jeopardizing consumer safety; and

Result in consumer deception, when, for example, manufacturers do not verify the identity of their raw materials.

Take action against claims in cases involving serious risk of harm to the consumer (such as egregious claims of benefit in treating serious diseases) or widespread economic fraud.