IIVS | Management
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Management

Rodger D. Curren, PhD

Rodger D. CurrenChief Executive Officer and Chairman of the Board

Dr. Rodger Curren co-founded IIVS and currently serves as CEO and Chairman of the Board of Directors.

After more than 10 years of specializing in genetic toxicology and chemical carcinogenesis, Dr. Rodger D. Curren created an In Vitro Toxicology Division as part of the contract research organization Microbiological Associates (now BioReliance) in 1988. This activity was subsequently incorporated as its own non-profit Institute, the Institute for In Vitro Sciences, Inc. (IIVS) in 1997. The goal was – and still is – to provide educational and laboratory-based resources for non-animal safety testing to industry, government, and animal welfare organizations, as well as the general public.

In addition to Dr. Curren’s work with IIVS, he serves on many national and international committees and science advisory boards of organizations focused on the development, validation, and practical use of alternative methods to whole animal testing. Among other activities, he is past president of the American Society for Cellular and Computational Toxicology (ASCCT), and a former member of both the Scientific Advisory Committee for the European Center for the Validation of Alternative Methods (ECVAM) and the Scientific Advisory Committee for Alternative Toxicological Methods in the US. He currently serves on the Advisory Boards of the Center for Responsible Science and the International Foundation for Ethical Research.

Dr. Curren’s efforts in optimizing and promoting new alternative methods have earned him several honors in the in vitro field, including the Russell and Burch Award, the Bjorn Ekwall Memorial award, and the William and Eleanor Cave award for outstanding achievements in the development, validation and advancement of humane alternatives for product testing.

Dr. Curren received his B.S. (Biology) from Purdue University, followed by an M.S. from Ohio University and a Ph.D. in microbial genetics from the Institute of Microbiology at Rutgers University. His post-doctoral work (human cell mutagenesis and DNA repair) was conducted at the Michigan Cancer Foundation and Michigan State University.

Erin H. Hill

Erin H. HillPresident

Ms. Hill co-founded IIVS in 1997 with Dr. Rodger Curren where she is currently President and a member of the Board of Directors. As President, Ms. Hill is responsible for planning, directing and coordinating activities to achieve IIVS’ mission of increasing the use and acceptance of in vitro methods. She also interacts with other groups, both domestic and international, who are involved the advancement of non-animal alternative methods with the intent of coordinating efforts leading to the regulatory acceptance of these methods.

Prior to co-founding IIVS, Ms. Hill worked for a tissue engineering company (Advanced Tissue Sciences) where she assisted with the marketing and sales of 3-Dimensional human skin constructs to the personal care and household products market. Ms. Hill then expanded her interest in in vitro methods during work for a developer of hollow fiber bioreactors for the production of mono clonal anti-bodies. In 1995 she joined the In Vitro Toxicology Unit at Microbiological Associates with Dr. Rodger Curren.

In 2010 Erin co-founded the American Society for Cellular and Computation Toxicology (ASCCT) where she serves as Treasurer. She is also a board member of the In Vitro Testing Industrial Platform. Erin receiving her bachelor’s degree in 1990 in Cell Biology and Biochemistry from the University of California, San Diego.

Hans A. Raabe, MS

Chief Operating Officer and Treasurer

As Vice President and Chief Operating Officer, Mr. Raabe is responsible for the development, design, operation and improvement of the systems that create and deliver in vitro testing services. Mr. Raabe has served as an expert on several OECD Test Guideline panels, has been an invited presenter at ICCVAM Workshops and review panels, and has participated in multiple ECVAM and ICCVAM validation studies.

Mr. Raabe joined the newly-formed IIVS in 1997 as Study Director for GLP-compliant ocular and dermal irritation assays. Prior to joining IIVS, Mr. Raabe worked for Microbiological Associates, Inc. (now BioReliance Corp.) in the Genetic Toxicology Division where he conducted and supervised in vitro and in vivo toxicity and DNA damage detection assays.

His research interests include modeling ocular and dermal irritation and wound healing events in vitro using complex 3-D tissue constructs and ex vivo tissues. He has been an SOT member since 2008.

Mr. Raabe received his BS degree in Zoology from the University of Maryland in 1984 and a MS in Biotechnology Management at the University of Maryland, University College in 1996.

Greg Mun, BA

Greg MunLaboratory Manager

Mr. Mun is responsible for the overall operations of IIVS’ commercial contract laboratory activities, the scheduling of reconstructed tissue testing activities, and the technical transfer, optimization and validation of new and emerging in vitro applications.

Greg has been with IIVS since its beginnings in 1997. He has extensive experience with GLP-compliant contract laboratory services as a technician, laboratory manager, and study director. Greg experience also includes training of technicians in 3-D assay systems, the BCOP assay, and sterile tissue culture training, and participation in projects such as the Reconstructed Skin Micronucleus Assay. Greg received his BA degree in Biochemistry from the University of Virginia in 1988.

Amanda Ulrey, RQAP-GLP

img_7305-web-copyDirector of Quality Assurance

Ms. Ulrey is the Director of Quality and Compliance for IIVS, assuming responsibility for instituting and fostering a culture of quality management and compliance throughout the organization. She provides leadership, training, and oversight of the Quality Assurance Unit, and institutes and maintains policies and procedures for regulatory compliance and organizational quality management.

Ms. Ulrey is a member of the Society of Quality Assurance (where she is currently a member of the Mentoring Program Committee, Computer Validation Initiative Committee, and GLP Specialty Section) and the American Society for Quality. She has given several presentations and authored posters on the topics of the application of GLPs to in vitro studies and the importance of supplier qualification programs.