FDA approved Singapore work trip during government shutdown, records show

SINGAPORE — Sentosa Island boasts the luxury, five-star Ora and Michael hotels, with palm-tree-lined pools, lobbies flanked with luxury stores, and a casino that adjoins both hotels and buzzes with gamblers. The Singapore resort is also where a group of federal employees from the U.S. Food and Drug Administration were sent for a work trip in the final hours of the government shutdown. 

Internal FDA records obtained by CNBC show 31 agency staffers traveled to Singapore in mid-November for a conference of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use, or ICH — a trip that cost more than a quarter of a million dollars, or upward of $8,000 per person, according to the documents. The travel was approved when the agency was operating with reduced staffing and limited resources in part due to the shutdown. 

The FDA is under significant pressure. The Trump administration proposed an 11.5% cut to the FDA’s budget this year. Nearly 1,900 staffers were laid off, and around 1,200 others took early retirement packages, according to May testimony from FDA Commissioner Marty Makary. In addition, senior leadership has been in upheaval, and former FDA chiefs have publicly questioned the agency’s handling of key issues such as vaccine policy. 

The FDA attendees at the Singapore conference ranged from deputy directors to a program coordinator, records show. Their travel was approved about one week before the end of the government shutdown — the longest in U.S. history, at 43 days. Most staffers departed on Nov. 12, the same day the U.S. House of Representatives voted to end the shutdown, and the remaining travelers left Nov. 13 and 14, according to the documents. 

The ICH, registered as a nonprofit under Swiss law, says it aims to unify the global standards for drug development and approval. The conference, held Nov. 18-19, took place in a series of meeting rooms on the island resort grounds.

ICH told CNBC in an email that “approximately 500 people attended in person,” including regulators and pharmaceutical industry experts from around the world. It also wrote that the “FDA is one of the founding members of ICH” and helps develop the requirements for “safe, effective, and high-quality pharmaceuticals.”

As part of the November assembly, three guidelines were adopted that aim to streamline global drug development and safety monitoring, according to the ICH. In a follow-up email, the organization said the first guideline provides a template to eliminate “inconsistent formats” in clinical trial protocols and ease electronic data sharing. The second seeks to ensure…