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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 in
respect to alcohol in an early paper by Dr.
Mullen).
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 ("AUC" in
exposure assessment)
- Compartmental models
(including criteria for choosing the
"best" model)
- Elements of "PBPK"
modeling & its comparison with
empirical modeling
- Steady-state concepts
(multiple dosing)
- Bioavailability &
bioequivalence
- Noncompartmental
analysis (mean residence times,
etc.)
- Fraction absorbed
(Wagner-Nelson) plots
- Drug metabolism
(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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July 9 - 11, 2012
Acadia University (click HERE to visit
Acadia University's website)
Wolfville
Nova Scotia
Canada B0P 1X0
REGISTER FOR
THIS COURSE
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