George P. Larrick
8/12/1954 - 12/27/1965
George P. Larrick was born on November 19, 1901 in Springfield,
Ohio. He worked his way through two years at Wittenberg College
from 1919-1921, and then took a pre-med course at Ohio State University
from 1921-1923. In 1923, he accepted a "temporary job"
as a food and drug inspector in Cincinnati. Fascinated with the
work, he abandoned his medical aspirations, and successfully passed
the competitive Civil Service exam for a permanent appointment.
By 1930, he had been appointed senior food and drug inspector. In
1937, he was responsible for dispatching very nearly the entire
field force of the FDA to track down remnants of the poisonous Elixir
Sulfanilamide which killed 109 people, and dramatized the need for
premarket testing of new drugs. Larrick was also responsible for
assembling an exhibit, dubbed by reporters, "The Chamber of
Horrors," which effectively documented the need for a new federal
food and drugs act. In 1939, following enactment of the new Food,
Drug, and Cosmetic Act, he was appointed Chief Inspector of the
Food and Drug Administration. In addition to directing FDA investigations,
he served as acting director of the Drug Division for a time, and
early during World War II, assisted in the organization of the Procurement
and Assignment Service of the Office of Defense, Health and Welfare
Services.
Following the war, he served as Assistant Commissioner, Associate
Commissioner and finally Deputy Commissioner of the Food and Drug
Administration. In 1954, he was appointed Commissioner, succeeding
Charles Crawford. Commissioner Larrick headed the FDA during the
period of its greatest growth. In 1954, the Agency had less than
1,000 employees to regulate more than one fourth of the nation's
commerce in consumer goods. The First Citizen's Advisory Committee
report became the blueprint for extensive changes in the organization
and a rapid increase in its resources. During Larrick's tenure,
FDA appropriations increased more than tenfold, from 5 million to
over 50 million, and its staff expanded to almost 4,000. The building
program inaugurated during Larrick's administration provided modern
laboratories for a majority of the FDA field districts and a $25
million headquarter's laboratory. His last official act was its
dedication in December 1965.
Larrick was noted for his ability to maintain good relations with
Congress and major amendments began to transform the 1938 Act from
a primarily punitive law to one designed to assure consumer protection
by preventing violations. During Larrick's administration, however,
the FDA came under strong criticism from some members of Congress.
One of its strongest critics was Senator Hubert H. Humphrey, who
accused the agency of showing lax management, having ineffective
leadership, of being slow moving, and of lagging in scientific work.
Mr. Humphrey and others called for "new and dynamic leadership."
Larrick counted among his friends, however, Rep. John E. Fogarty
(D-RI), the powerful chairman of the House Appropriations subcommittee.
Larrick's administration oversaw the 1959 cranberry recall due
to residues of the carcinogenic pesticide aminotriazole; the issuance
of a public warning against the Hoxsey cancer treatment and legal
actions against Krebiozen, another false cancer treatment; prohibition
of thalidomide as a human teratogen in 1961, and the passage of
the Kefauver Harris Drug amendments in 1962 in response to the thalidomide
crisis. Attention was focused on drugs and the drug approval process
beginning with revelations that William Welch, the agency's chief
of the Antibiotics Division, had accepted nearly one-quarter of
a million dollars for editing private promotional journals in his
field while passing judgement on the products in his position at
FDA. Congressional investigations into thalidomide brought accusations
that drug manufacturers had too easy access to regulators and could
thereby exert undue influence upon the review process. Although
Larrick assured Congress that drug approvals had not been superficial,
testimony was heard alleging that lay administrators were not really
able to evaluate major drug review problems which were "all
of a medical nature and exceedingly complex." Calls for Larrick's
resignation were accentuated with recommendations that the next
commissioner be a physician.
When Larrick announced his intentions to retire in 1965, John
Gardner credited Larrick with great progress in administering the
law, noting that "despite the twin handicaps of inadequate
resources and inadequate legal authority, FDA has achieved remarkable
success in its mission."
After he retired from active service, Larrick became a consultant
on food and drug law and administration until he died. In this capacity,
he made a study for the Pan American Health Organization on the
feasibility of a central food and drug laboratory for South American
countries. The Drexel Institute of Technology conferred on him an
honorary Doctor of Science in 1955, and in 1968 he was recognized
by AFDO as a "catalyst who consistently brought about constructive
change, and a skilled administrator in a field that requires experience,
courage, respect for the rights of the regulated, and faith in the
due process of law." Larrick died on August 13, 1968.