Training School:The Center for Professional Advancement  Northbrook, IL, United States http://www.cfpa.com
Jobs & Resumes: Northbrook Houses & Roommates: Northbrook
Total 113 program(s)/course(s) available.
Atomization, Sprays and Atomizers Atomization is an important process used in many industries, including chemical, petrochemical, biochemical, medical, food, paper, combustion, fuels, and agriculture. This course provides an introduction to atomization for engineers, scientists and technologists who are interested in or need to know more about atomization, atomizer design, atomizer specifications and selection for various appli......
Starch: Chemistry, Properties and ApplicationsThis course covers the fundamental structure, chemistry, functional properties of starches and their utilization in food applications. The course also reviews the various types of starches and factors that should be considered when choosing and using starches. The application of starches in many food systems is presented in depth. There will be a demonstration of food starches. The most current......
GMP for Dietary SupplementsThis two-day course will cover regulatory and legal aspects of GMP¡¯s for dietary supplements. It will provide a comprehensive introduction and a ¡°how to¡± program for implementation. Participants will understand issues involved in manufacturing and testing of dietary supplements. They will become familiar with FDA expectations when performing audits of dietary supplement companies. A rational ap......
Powder Mixing TechnologyThe course presents the principles and techniques of mixing free-flowing or cohesive powders. Selection of suitable industrial equipment for particular mixing duties will be discussed analyzing mixer performance in terms of process advantages, mixture quality and the flexibility of the mixer for multi-product manufacture.
Other topics to be covered include powder sampling techniques, a pract......
Industrial Drying of Heat Sensitive MaterialsThis course describes the aspects of achieving successful drying operations involving heat sensitive materials, especially where dryer feedstocks are available as a liquid formulation or as a moist solid particulate. Another major focus is the drying of such difficult-to-dry materials as foams and extremely dense large particulates. Reference will be made to the relevant drying theory, and the ......
Color Additives and Their Use in Decorative CosmeticsThis course provides a comprehensive look at the broad spectrum of color additives that are used in decorative cosmetic products, including standard organic and inorganic pigments as well as pearlescent, fluorescent and surface treated ones. Starting with a discussion of color basics from a physics perspective, it then moves to the selection of colors from the viewpoints of regulations, stabili......
Process Analytical TechnologyBoth the US Food and Drug Administration and the European Medicines Agency are pushing improvements in pharmaceutical manufacturing efficiency, defined as Process Analytical Technology, or PAT. These initiatives are driven by increased regulatory demand, consumer pressure and soaring drug dosage costs. The regulatory agencies have identified the test-to-document requirements of the old cGMP man......
Aerosol TechnologyThis course has been designed to cover the major aspects of aerosol technology and to instruct you in the successful formulation of aerosols for use in personal care products (deodorants, hair spray and shaving lathers), household products (room deodorants and disinfectants), automotive products (cleaners, lubricants and refrigerants), paints, food products (including pan sprays), industrial/ i......
Emulsion-SuspensionThis course emphasizes the application of emulsion and suspension principles to the solution of practical, technological problems in the preparation and evaluation of pharmaceutical, cosmetic and related personal care products. Throughout the course, the interrelationship of the many specialty areas involved in emulsion and suspension products will be stressed. Newer technologies such as microe......
Good Laboratory Practices (GLP)The main intent of this course is to review the requirements imposed by Good Laboratory Practice (GLP) regulations for facilities engaged in, toxicology and product safety testing, primarily in animals and biological test systems. The responsibilities and functions of management, the Study Director, Principal Investigator and the Quality Assurance Unit (QAU) will be covered. Various procedures ......
cGMP for Pharmaceutical Production SupervisorsThis course will provide an orientation and understanding of the Current Good Manufacturing Practice segment of the U.S. Food, Drug, and Cosmetic Act. The course will cover supervisory techniques and practices for complying with the U.S. FDA regulations in packaging, assembly, production and manufacturing. It will provide a practical application of the cGMP on the operating level. Actual experi......
Critical Process Cleaning and Cleaning ValidationThis course will provide a solid overview of the principles and technology of residue removal and residue measurement on product contact surfaces. It will address the latest issues, industry practices and compliance strategies regarding choice of cleaning techniques, cleaning agents, analytical methods, residue challenges, grouping strategies and validation protocols. Examples of current indust......
Pharmaceutical Quality Assurance and ControlThis course provides an understanding of the principles and practice of pharmaceutical quality assurance and control and of specific topics which have become important because of regulatory interest or recent technological achievements. Throughout the course an emphasis is placed upon quality as viewed on a cost/benefit basis as well as a cGMP basis.
The first day provides an understanding o......
Lyophilization TechnologyThis course is designed to provide participants with an up-todate understanding of the theory and practice of lyophilization. Freeze-drying (lyophilization) will be presented and explained in physical, physicochemical, biochemical and engineering terms. Theory and practice will be interrelated and biotechnological and pharmaceutical applications will be emphasized. Participants should acquire a......
System Validation, GAMP Harmonization and P.A.TThis course is designed to provide the basics of computer system validation. Utilizing lectures, discussions, hands on exercises, the class will address the rules, tools and techniques needed to develop, manage, and conduct a validation process and project. The program focuses on the best validation practices utilizing, Risk assessment, PAT, GAMP 4 and more. Included in this comprehensive cours......
Granulation, Tabletting and Capsule TechnologyThe main aim of this course is to review the science relating to tabletted and encapsulated pharmaceutical products. The course begins with a consideration of raw material testing and the basic aspects of powder and granulation technology, progresses through formulation of solid dosage forms to manufacturing processes and equipment including scale-up and technology transfer. The program conclud......
INDs, NDAs vs CTDs Global RegulationsThe content of this course is designed to present the intricate parts of INDs, NDAs, BLAs, ANDAs, SNDAs and CTDs. These regulatory submissions for drug and biologic products will be based on the requirements of the US Code of Federal Regulations, the ICH Guidelines for global submissions and the EU Directives. Specifics of the IND, NDA, BLA, ANDA, SNDA and CTD will be detailed for safety, quali......
Patent LawThe U.S. Court of Appeals for the Federal Circuit is the focal point for the legal criteria by which US patents are enforced. The Court¡¯s rulings on recent multi-million dollar patent infringement awards illustrate how important it is for the business manager to understand how the patent system works.
With the great increase in the cost of technology development, and the rapidity of technica......
cGMP Auditing - Strategies for ComplianceThis practical, introductory course was designed to provide a mechanism for those interested in understanding the basic requirements for auditing in the pharmaceutical and related industries.
The course presents an introduction to the evolutionary process of FDA regulations and describes in detail the latest FDA initiatives in the inspection process. It provides a road map for auditors in se......
Preparing for and Surviving an FDA InspectionThis course provides a background and understanding of the role played by the Agency, it¡¯s administrative and enforcement powers. It takes the participant step by step through the entire inspection process and describes various types of inspections, i.e. pre-approval inspections (PAI), routine GMP inspections, bioresearch monitoring inspections, quality systems inspections techniques (QSIT) app......
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