The White House issued an executive order in 2015 to review and revise the biotech approval system that pretty much everyone agrees is broken. In the United States, GMOs have been regulated under the Coordinated Framework for the Regulation of Biotechnology, issued in 1986 and updated in 1992. As the White House noted, that “update affirmed that Federal oversight should focus on the characteristics of the product and the environment into which it is being introduced, rather than the process by which the product is created.”
Under the coordinated framework, regulation of genetically engineered crops and animals has been cobbled together under the jurisdiction of three different government agencies: The Department of Agriculture, with existing authority to regulate “plant pests,” approves all releases of GMOs to make sure that they don’t create an environmental hazard. The Environmental Protection Agency, with authority over pesticides, must approve all crops that contain insect-killing genes. And the Food and Drug Administration is responsible for evaluating whether GMOs are safe to eat. A new GMO product can fall under the jurisdiction of only one or as many as all three of the agencies, depending on what is being developed. A new crop that’s going to be used both for human food and animal feed, for example, might fall under jurisdiction of all three.
GMO crops are treated much like any other food. If it turns out that they cause health problems, the FDA can order them taken off the market, but the FDA does not currently require biotech companies to submit these crops for approval before they go on the market. Although formal studies are not required, biotech companies developing a new GMO have waited for the FDA to issue a letter certifying that the agency has looked at the product and found no safety issues with it.
The White House has now urged federal agencies to draw up new regulations to focus on “transparency,” “predictability” and a commitment to “reduce uncertainty in their regulatory processes.” The U.S. historically has taken a product-focused “risk based” approach based on weight of evidence. But competing agencies and campaigning pressure from anti-biotechnology groups has resulted in the adoption of more precautionary views in recent years. It’s not clear whether the U.S. will also embrace a European-style process-based approach going forward.
The devolution of the oversight system over the past 30 years has dramatically slowed the adoption of new GM seeds and animal products. From 1988 to 1997, it took an average of 3.6 years to gain approval for a new GM product. (In addition to the half dozen or more years spent in research and development) But from 1998 to 2015, that wait time stretched to 6.8 years (13 years total including R&D) at an average cost of $130 million according to research by economists at the management school at Queen’s University.
While plants have a clear, if torturous, path to approval under the framework, GM animals must travel through regulatory no-man’s land. Animals are overseen by the FDA as drugs. The FDA has approved only two products an anticoagulant derived from the milk of transgenic goats and the AquaBounty salmon, which grows twice as fast as a non GMO version.
The salmon approval process took 20 years, a time frame that only multinational corporations with deep pockets can afford. (The entrepreneurial start up AquaBounty was taken over by Intrexon when it became clear it did not have the resources to press the regulatory process). Even after jumping regulatory hurdles, politics can intervene. Writing in the Genes and Science, Forbes and Slate (detailed in December 2012), the GLP’s Jon Entine exposed how White House politics blocked formal approval of the fish even after it was approved by the FDA. The GM salmon is still years away from making it to consumers’ plates.
Things are even more complex in Europe, where anti-GMO sentiments have created a cumbersome landscape in which cultivation is widely banned even as those nations import significant amounts of GMO animal feed. As in the U.S., the approval process in the E.U. has both scientific and bureaucratic stages. But there also is a political stage. Even after the European Food Safety Authority signs off on a new crop, it still must be approved by a legislative body the Standing Committee on the Food Chain comprising representatives from each of the E.U. nations.
The approval time is currently less than it is in the U.S., coming in at just under 5 years, according to the Queen’s University study, but that is because the GM products being evaluated are for import, not cultivation.
Some of the information generated for approval in the E.U. relies on information generated for the approval process in the U.S. Further, applications in the U.S. almost always include field trials as applications include cultivation, while the majority of the applications for approval in the E.U. are for “import and processing” and not for “cultivation.” Thus, we avoid a statistical comparison of their total approval time as it would be theoretically flawed.
The situation in Europe is just one example of another regulatory problem faced by biotech pioneers. Even after a new trait has been approved in the U.S., that doesn’t necessarily mean the seeds are ready to be marketed. Given the global nature of today’s grain markets, approvals must also be gained from nations who want to import the GM product, usually to be used as animal feed.
Otherwise companies run the risk of finding themselves in the ugly situation encountered by Syngenta in 2013, when it sold a new corn seed that had not yet been approved in China. The corn, MIR 162, was approved in the U.S. in 2010. China, which is known to be slow with its GMO approvals, rejected thousands of tons of corn after testing revealed traces of Syngenta’s new seed. That, in turn, prompted lawsuits against Syngenta by corn growers, grain handlers and feed companies.
The overall issue of R&D cost was examined in a 2011 study for Crop Life International by Phillips McDougal, a consulting firm in the United Kingdom. The firm surveyed several of the major industry players, including Monsanto, Dow AgroSciences, Syngenta and Bayer CropScience, to develop a better picture of the price tag associated with bringing a new trait to market. The mean cost was $136 million. Among the biggest factors: $31 million for discovery, $28 million for breeding and field testing (to meet regulatory expectations), and more than $35 million for directly engaging the regulatory system. And that last segment may be on the rise:
Based on the results of the survey into the actual time associated with each activity stage of the R&D process, the overall time involved in regulatory testing and approval appears to have increased. If this trend is real and continues it could have a significant impact on the cost of regulatory testing and authorization in future years.
The high cost both in terms of time and money to bring a new GM trait to market is often cited as one of the limiting factors in developing plants and animals that could offer a wide range of benefits to the world.
Some GMO supporters point to the Rainbow Papaya as example of what genetic modification could do in a friendlier regulatory environment. The fruit was engineered to be resistant to ringspot virus, which had threatened to wipe out Hawaii’s papaya industry in the 1980s and 90s. The plant was developed by a university researcher with an assist from Monsanto, which provided its licensed technology for what the New York Times described as “almost nothing” (Monsanto receives no money from the cultivation or sale of the papaya.)
The fruit found a smooth path to commercialization. According to its inventor, plant pathologist Dennis Gonsalves, the papaya received its approvals from the FDA, EPA and USDA just two years after the start of the regulatory process allowing a much faster recovery by the island state’s papaya industry.
Economists and industry experts say the current cost/time equation is a contributing factor in the decisions by Monsanto and other large companies to focus most of their attention on products with the highest potential financial returns. It doesn’t make financial sense, for example, to spend $135 million developing a new variety of wheat that’s resistant to a pest found only in a few Wyoming fields or a fruit with a tiny market share. And there aren’t many small firms with the capital required to develop a new commercial GM trait. Peter Phillips, a public policy professor at the University of Saskatchewan, says regulatory over-reach is limiting innovation:
A patchwork of poorly harmonized global regulations incentivize biotech companies to bypass smaller markets, placing crop and nutritional benefits and innovations out of reach of consumers and farmers with the greatest need. Regulatory programs that ensure timely review and public policy approaches that provide stability in the process will incentivize innovative companies of all sizes to pursue ongoing advances in biotechnology innovation and research.