Training Course:Preparation, Packaging and Labeling of Clinical Trial MaterialsSchool/Trainer:The Center for Professional Advancement
New Brunswick, New Jersey, United States
Course Format: Classroom | E-learning | Virtual Class | Online | On-site | Blended | Self-paced
Course Description:
'' The aim of this comprehensive course is to provide an introduction to the many details that must be considered in the design, preparation, packaging, labeling and distribution of clinical trial materials in support of adequate and wellcontrolled clinical studies. Emphasis will be given to practical examples of procedures, components, and regulatory requirements needed to provide acceptable investigational materials. Comparison of the requirements of the United States and Europe and consideration of the harmonization of international clinical studies will be given.
The interrelationships of the industrial pharmacist, clinical research associate, medical monitor, regulatory officer, clinical pharmacist, clinical supplies and quality assurance/control personnel will be discussed. In addition, cGMP will be reviewed to ensure compliance during the preparation, use and return of the trial materials.
The course provides participants the opportunity to share experiences with faculty and colleagues about effective methods to design, produce, package, and label clinical trial materials. The concepts presented during the course are integrated by means of case studies that consider real-world clinical trial supply problems and solutions.
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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: New Brunswick
Houses & Roommates: New Brunswick
Other training courses offered by The Center for Professional Advancement:
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
Good Clinical Practices (GCP)
Quality Audits
Packaging of Pharmaceuticals
Tablet Production for Operators and Supervisors
Pharmaceutical Technology Transfer
ICH-Q7A
IQ, OQ, PQ
ICH Q10: Pharmaceutical Quality System
Current Good Manufacturing Practice (cGMP) for Purchasing
Excipient GMPs
Sulfonation and Sulfation
Pharmaceutical Process Development
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