Training Course:ADME: Absorption, Distribution, Metabolism and EliminationSchool/Trainer:The Center for Professional Advancement East Brunswick, New Jersey, United States
Course Format: Classroom | E-learning | Virtual Class | Online | On-site | Blended | Self-paced
Course Description:
'' The course will provide participants with an understanding of the principals and fundamentals for absorption, distribution, metabolism, and the elimination (ADME) of pharmaceutical chemicals. The actual dose of a drug that ultimately reaches the target tissues and exerts pharmacologic or toxicologic effects is highly dependent on the kinetics of drug absorption and disposition in the body. Many factors can influence these kinetic processes. The goal of the course is to provide training in the fundamentals of ADME that should be understood for those involved in drug development and clinical applications. The thrust of the discussions will pertain to drugs, although the concepts are appropriate for all chemical entities. Some modeling and mathematical formulations will be presented; however, the lack of mathematical background will not impede one¡¯s ability to understand the concepts involved. Finally, a few practical examples of the ADME of drugs will be provided to illustrate how the principles are applied in real life situations. ...''
Please go to the school's official website for training price and schedule: http://www.cfpa.com
Phone:(732)238-1600
School Address:
Corporate Office Box 7077, 44 West Ferris Street East Brunswick, NJ USA 08816-7077 Phone: (732)238-1600 Fax: (732)238-9113 Email info@cfpa.com
Europe Office Oudezijds Voorburgwal 316A, 1012 GM Amsterdam, The Netherlands Phone +31/20/638.28.06 Fax +31/20/620.21.36 Email amsterdam@cfpa.com
Jobs & Resumes: East Brunswick Houses & Roommates: East Brunswick
Other training courses offered by The Center for Professional Advancement:
Project Management
Risk Analysis & Human Factors Engineering
Gums and Hydrocolloids
Microencapsulation and Particle Coating
Documentation Management and Control
Analytical Methods Validation for FDA Compliance
Drug Product Stability and Shelf-Life
Microbiological Control and Validation
Process Validation for the Pharmaceutical and Medical Device Industry
Non-Clinical Drug Safety Evaluation and Drug Development
Root Cause Investigation for CAPA
Complaint Procedures for Medical Devices
Early Stage Clinical Studies for Drugs and Devices
Drug Delivery Technologies
Drug Specifications for APIs and Drug Products
The Quality System
Good Clinical Practices (GCP)
Generic Drug Approvals
Generic Drug Approvals
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