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PHARMACOKINETICS: Essential Theory and Practical
Considerations //
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Enhance
your appreciation and
understanding of pharmacokinetics by attending this unique three-day
course in Nova Scotia's charming and historic Annapolis Valley.
THE COURSE IN CONTEXT //
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As every scientist in the
pharmaceutical industry knows, the pharmacokinetics of a drug
must be thoroughly studied before it has any chance of reaching the
pharmacists' shelves.
Early clinical trials are undertaken primarily to determine the
pharmacokinetic parameters characteristic of each new pharmacological
entity. The applications of pharmacokinetics, of course, extend beyond
research and development to routine clinical practice where clinical
pharmacokinetics is utilized in devising individualized dosing
regimens, particularly for chronically administered drugs with low
therapeutic indices.
Given its importance in drug research and its relevance to modern drug
marketing, it is imperative that key scientific, clinical and marketing
staff members within the innovative pharmaceutical industry have at
least a basic understanding of the science of pharmacokinetics.
Highly regarded by hundreds of former attendees from both the
pharmaceutical industry and government agencies, this popular course
has been presented at various venues internationally (Canada, the USA,
the U.K. and Brazil)
since 1987.
FOR WHOM INTENDED //
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This course will be of particular interest to pharmaceutical
scientists, pharmacists, toxicologists, physicians and clinical /
regulatory personnel from the pharmaceutical and allied industries and
government regulatory agencies.
Of course, pharmacokinetics (toxicokinetics) has numerous applications
in the biomedical sciences generally. For example, this course is
also of special relevance to those engaged in emergency and forensic toxicology (viz.
"forensic pharmacokinetics", a term introduced by Dr. Mullen in 1977).
PARTIAL COURSE CONTENTS //
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- Physico-chemical determinants of drug
disposition
- Kinetics of drug absorption, distribution &
elimination ("ADME")
- First order rate constants and half-life
- Apparent volume of distribution
- Clearance concepts
- First-pass effects
- Area under concentration-time curves (exposure
assessment)
- Compartmental models (including criteria for choosing
the "best" model)
- Steady-state concepts (multiple dosing)
- Bioavailability & bioequivalence
- Noncompartmental analysis (mean residence times,
etc.)
- Fraction absorbed (Wagner-Nelson) plots
- Drug metabolism (a.k.a. biotransformation)
- Drug protein binding
- Causes of pharmacokinetic variability
- Toxicokinetics
- Pharmacokinetics computer programs
(Note: This
course requires no special mathematics prerequisite.)
PRINCIPAL
INSTRUCTOR > Peter W. Mullen,
Ph.D.
SUMMER
VENUE
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August 9 - 11, 2010
Acadia University (click HERE to visit Acadia University's
website)
Wolfville
Nova Scotia
Canada B0P 1X0
To
register for this course CLICK HERE.
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