DESCRIPTION
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Drug Dissolution Testing and Establishing Plasma Drug Levels in Humans
Drug dissolution testing is an essential and critical step for appropriate and efficient product development such as tablet and capsule.
This seminar will provide relevant pharmacokinetics and physiological background so that making this choice becomes easier and instinctive.
No prior knowledge of pharmacokinetic and/or physiology is required; however
Seminar Instructor Dr. Qureshi has extensive (30+ years) working experience, as a research scientist, with a regulatory agency (Health Canada).
Learning Objectives:
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Physiological and Pharmacokinetic Principles:
Related physiological terms: GI tract environment, drug absorption, permeation.
Pharmacokinetic principles including terminologies of plasma drug concentration-time profiles/curves, rates of absorption and elimination, Cmax, Tmax, half-life, AUC, apparent volume of distribution, bioavailability/bioequivalence, etc.
Defining and differentiating drugs/medicines and drug/medicinal products
Defining quality of drugs/medicines and drug/medicinal products.
Who will Benefit:
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Pharmaceutical Development
Setting up analytical methods (pharmacopeial, regulatory or in-house developed)
R & D, both analytical and formulation
Project Management
Quality Control
Quality Assurance
Regulatory Affairs
Please contact the event manager Marilyn below for the following:
- Discounts for registering 5 or more participants.
- If your company requires a price quotation.
Event Manager Contact: marilyn.b.turner(at)nyeventslist.com
You can also contact us if you require a visa invitation letter, after ticket purchase.
We can also provide a certificate of completion for this event if required.
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For more information: https://www.eventbrite.com/e/drug-dissolution-testing-and-establishing-plasma-drug-levels-in-humans-com-a-tickets-43249827398?aff=RMV
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