Take advantage of our $1507.50 price by registering early!
* After Friday, December 20, 2019, costs are $1687.50.
course is designed to introduce basic pharmacology concepts which are utilized
in drug development and clinical research to non-clinical professionals. Topics
will include the basic principles of pharmacology and overview of several major
classes of therapeutic agents, with attention to their mechanisms of action.
Issues of current and future directions in pharmacology will be addressed,
including the sources of information about pharmacologic agents, the ethics of
human experimentation, the drug development process, and new biotechnological
approaches to drug design.
- Become familiar with the concepts of
pharmacokinetics and pharmacodynamics
- Develop knowledge regarding several
major classes of therapeutic agents and understand their mechanisms of
- Gain an in depth understanding about
pre-clinical research and steps necessary for transition to clinical
phases of the drug development process
- Become familiar with the concept of
molecular targeted therapeutics
- Review of Investigator’s Brochure
(IB) contents and the Investigational New Drug Application (IND)
- Critique and analyze information
obtained from scientific literature and demonstrate an understanding of
the pharmacology parameters
or Project Team Leaders who will be managing projects
- New Clinical, Regulatory, and Department Staff who will design
clinical trial programs
- Clinical Research Associates, Data Managers or others interested in
transitioning into clinical trial management
- Grant Administrators
- Medical Directors
- Medical Writers
- Regulatory Affairs Professionals
- Research and Development Personnel
The course will be led by one of the following
Malikova, Ph.D., MSci, M.A., C.C.R.A., RAC
Click here for complete trainer
1: 8:30 a.m. – 5:00 p.m.
- Introduction: The Heritage of Pharmacology
- Sources of Information about Drugs
- Drug-Receptor Interactions
- Overview of pharmacology parameters utilized in the drug
development process (i.e. half-life of the drug, plasma concentration,
therapeutic index, area under the curve (AUC), effective concentration
EC50, etc.) Regular Copy
- Principles of Pharmacokinetics (PK studies): Drug Absorption, Distribution, Metabolism and
Elimination (ADME parameters overview)
- Pharmacodynamics (PD studies): Dose-Response Relationships; Time-Concentration
- Drug Interactions: CYP enzymes and their role in drug metabolism and
drug-drug interactions and side effects
- Overview of Investigator’s Brochure contents and Investigational
New Drug Application (IND)
2: 8:30 a.m. – 5:00 p.m.
- Principles of Endocrine Pharmacology
- Pharmacology of the Autonomic and Peripheral Nervous System
- Central Nervous System Pharmacology
- Pharmacology of Pain and Inflammation
- Principles of Cardiovascular Pharmacology
- Principles of Chemotherapy
- Molecular targeted therapeutics for cancer treatment
- Review of Investigator’s Brochure: Create
checklists that encompass timelines and sections needed from different
- Interactive Discussions
- Questions and Answers
fees include assorted breakfast items that will be available each day ½ hour
prior to the start of the seminar. Also included is a Networking Lunch that
will be served each training day.
Special rates are available for
multiple attendees from the same organization.
Contact Melissa Dolen at 781-972-5418 to discuss your options and take
advantage of the savings.
Click here for our seminar
Barnett International is accredited by the
Accreditation Council for Pharmacy Education as a provider of continuing
pharmacy education. Participants will
receive 15 hours (1.5 CEUs) of continuing education credit for full
participation, including the completion of a pre-test, post-test, and program
evaluation. Barnett International will
issue a receipt of completion for earned CEUs within three weeks of program
completion. ACPE#: 0778-0000-19-048-L01-P.
this course at your company! For more information, contact Naila Ganatra at +1