CenExel Clinical Research, Inc., (“CenExel” or the “Company”) announced that Anaheim Clinical Trials (ACT), an adult and pediatric Phase I through Phase IV clinical research Center of Excellence, recently underwent three separate routine national agency audits within 45 days.
SALT LAKE CITY and ANAHEIM, Calif., Sept. 9, 2019 /PRNewswire/ -- CenExel Clinical Research, Inc., ("CenExel" or the "Company") announced that Anaheim Clinical Trials (ACT), an adult and pediatric Phase I through Phase IV clinical research Center of Excellence, recently underwent three separate routine national agency audits within 45 days. The three agencies responsible for the protection and promotion of public health included the US Food and Drug Administration (FDA); the European Medicines Agency (EMA); and, the Japanese Pharmaceuticals and Medical Devices Agency (PMDA). Each agency individually concluded their inspections citing no significant objections or violations. "This may be an industry record – three consecutive audits within 45 days by national agencies with no FDA Form 483 or equivalent notifications," said Patrick McLaughlin, CEO of ACT. "Moreover, these three audits were prompted by our high enrollment in multiple clinical trials. The consistent quality of the data and the rigor of our Quality Assurance program were highlighted during these pivotal audits. This is a well-deserved accomplishment for everyone at ACT." "Along with our nurses, doctors, and pharmacists, the hard work and continued dedication of each employee at ACT contributed to this successful outcome," added Dr. Peter Winkle, MD, FACG, FACP, CPI. "Our patients and sponsors have come to expect the high quality and outstanding service that ACT delivers." "As a member of the CenExel site network, ACT has certainly lived up to the Center of Excellence best practices from which the name 'CenExel' was inspired," said Tom Wardle, CEO, CenExel. The FDA and other regulatory agencies conduct periodic audits of clinical research sites for bioresearch monitoring purposes. A Form 483 is issued by the FDA upon completion of a facility site inspection, to document any concerns or observations found by the investigator which may represent violations of the US Food, Drug and Cosmetic (FD&C) Act. For more information, please contact Linda Gundaker, Executive Vice President, Business Development at ACT, via email at lgundaker@act-trials.com or mobile at 610-937-2006. About Anaheim Clinical Trials About CenExel Clinical Research
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