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| Drug Development |

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ReceptoPharm is developing proprietary
therapeutic protein products for the treatment of neurological,
viral and and autoimmune disorders. |
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| CRO Services |
ReceptoPharm offers a full range of contract
research services catering to small and start-up biotech companies. |
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Rik J. Deitsch has been the President,
Chief Executive Officer and a Director of
the Company since November 7, 2002. From
February 1998 through November 2002, Mr.
Deitsch served as the President of NDA Consulting
Inc., a biotechnology research group that
provided consulting services to the pharmaceutical
industry. NDA Consulting specialized in
the research of peptides derived from Cone
Snail venom, Cobra venom and Gila Monster
venom. Mr. Deitsch holds both a B.S. in
Chemistry and an M.S. in Biochemistry from
Florida Atlantic University and has conducted
clinical and laboratory research in collaboration
with scientists at Duke University Medical
Center and the Cleveland Clinic . Mr. Deitsch
is an adjunct professor and teaches several
courses for Florida Atlantic University's
College of Business and Continuing Education
Department.
Paul F. Reid, PhD. is a Co-Founder of ReceptoPharm.
From 1996 to May of 2001, Dr. Reid was an
independent consultant to several privately
held biotech companies where he used his
expertise to assist in corporate development,
strategic planning which included writing
business plans, estimating market valuations
for targeting potential venture capital
and corporate partners, and making presentations
to U.S. and European financial institutions.
Dr. Reid also advised his clients regarding
human and veterinary regulatory affairs
for the United States, Canada, and Europe,
and drug applications (pre IND, IND and
Orphan), drug production, new drug development,
clinical trial design, patient monitoring,
and experimental design.
From 1993 to 1996 Dr. Reid was employed
by the United States Medical Research Institute
for Infectious Diseases (USMRIID) at Fort
Detrick, Maryland, under a grant from the
National Research Council in Washington,
D.C. Under the grant he was responsible
for the expression and purification of a
variety of neuroactive components from snake
venom in bacterial and yeast systems and
purification of expressed material with
expansion to large-scale vaccine production.
From 1991 to 1993, Dr. Reid was employed
as a Post-Doctoral Researcher at Public
Health Laboratories in Port Down, England,
and Ruhr University in Bochum, Germany,
where he was responsible for converting
the laboratory to the utilization of genetic
techniques. Dr. Reid's Ph.D. studies centered
on investigating the activity and function
of neural ion channels. Dr. Reid has a Bachelor's
Degree in Microbiology from Trinity College
in Dublin, Ireland and his Ph.D. is in Neurobiochemistry
from Imperial College in London, England.
In addition, Dr. Reid has completed FDA
courses in current good manufacturing practices
(cGMP/cGLP) and the preparation of standard
operating procedures (SOPs) in accordance
with government guidelines.
Laurence N. Raymond, Ph.D. is a Co-Founder
of ReceptoPharm. From 1997 to May 2001,
Dr. Raymond was a consultant to BioTherapeutics,
Inc., also known as Phylomed, Inc., where
he was instrumental in the development of
monoclonal antibodies utilized in the investigation
of modified toxins as well as the development
of cell culture, immunochemical and receptor
based assays for examination of the therapeutic
applications of biopharmaceuticals.
Previously, Dr. Raymond was an Associate
Fellow at the Sandoz Research Institute,
a division of Sandoz Pharmaceuticals, where
he established and managed a laboratory
developing monoclonal antibody-based immunoassays.
Prior to that Dr. Raymond was Manager of
Research and Development for Pel-Freez Biologicals
in Rogers, Arkansas, and, simultaneously,
Director of the Hybridoma Lab at the University
of Arkansas Biotechnology Center in Fayetteville,
Arkansas. There he was responsible for establishing
and producing monoclonal antibody under
contract. Dr. Raymond developed techniques
in hybridoma creation and development as
well as protein purification and lymphoid
stimulation while at the University of New
Mexico School of Medicine in Albuquerque.
While at the Biophysics Technology Laboratory,
at the University of Arizona in Tucson,
he developed an adjunct system to plasmaphoresis
for the extra-corporal removal of plasma
proteins by electrodialysis to be applied
to the treatment of Waldenstrom's macroglobulinemia
and was applied to the model disease in
dogs. He was involved in rheumatoid arthritis
research with the Southwestern Clinic and
Research Institute in Tucson, Arizona, where
he developed his skills in tissue and cell
culture, mitogenic and antigenic stimulation
of lymphoid cells as well as in-vitro and
radio-assays. Dr. Raymond earned a Bachelor's
Degree in Nutritional Biochemistry, a Master's
of Science Degree in Animal Physiology and
a Ph.D. in Microbiology and Immunology all
from the University of Arizona.
Harold H. Rumph has been a director of
the Company since March of 2003 and bring
with him a career devoted to technical sales
and marketing. From 1988 to 2003 he was
founder and owner of a high tech business
providing computerized scheduling services
to the construction industry. From 1986
to 1988, Mr. Rumph was Director of Sales
and Marketing for JE Research, Inc. From
1980 to 1986 he was a founder, President,
and Director of Biogenix, Inc. This company
was involved in the development, manufacturing,
and marketing of in-hospital bedside and
ambulatory Patient Monitoring Systems. Biogenix
was also involved with research and development
of antiviral peptides from cobra venoms,
including clinical trials under FDA-issued
Investigational New Drug applications. Prior
to the above Mr. Rumph led sales teams and
was responsible for marketing at Harris
Communications, Harris Computers, Memorex
Corporation, Xerox Corporation, Cincinnati
Milacron, Amdahl Corporation, RCA Computers,
and IBM. Mr. Rumph received his BS degree
from the United States Naval Academy. |
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