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Biotechnology brochure - UCSC Extension Silicon Valley

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Molecular Diagnostics<br />

This survey course provides a foundation in the basic<br />

science and technologies that underlie the emerging<br />

field of molecular diagnostics, and highlights the<br />

potential impact on the health care landscape.<br />

The instructor examines the role of pharmacogenomics<br />

in the development of new therapeutics and<br />

treatment options. The instructor uses case studies<br />

to present the applications of molecular diagnostic<br />

tools in infectious disease identification and early<br />

detection and diagnosis of cancer. Also addressed<br />

are the regulatory challenges that face the new<br />

wave of diagnostic tests, and the global molecular<br />

diagnostics marketplace.<br />

Course 21972<br />

Nanotechnology, Introduction<br />

This survey course provides a foundation in the<br />

basic principles of nanotechnology. The instructor<br />

highlights recent advances in nanoscale science<br />

and engineering, drawing on examples and demonstrations<br />

from electronic, photonic, mechanical,<br />

chemical and biological systems. Participants learn,<br />

in each of these cases, how an understanding of the<br />

fundamental physical properties at the atomic level<br />

has permitted nanoscale engineering for specific<br />

applications. They gain an appreciation of the importance<br />

of reproducible manufacturing, in bottom-up<br />

and top-down approaches and self-assembly. The<br />

tools and methods used to characterize materials and<br />

devices at the nanoscale are explored. Instructors<br />

also discuss future prospects and possible roadblocks<br />

to implementation of nanotechnology, with reference<br />

to other technological advances in the last<br />

two centuries. Finally, local and national resources<br />

as well as key players are discussed.<br />

Course 4820<br />

Regulation of Drugs and Biologics<br />

This course helps participants understand the<br />

regulatory requirements, both U.S. and international,<br />

for patented and generic pharmaceuticals, over-thecounter<br />

drugs, and biological products. Students gain<br />

knowledge and insight into the regulatory agencies<br />

and their roles and responsibilities; regulatory applications<br />

and pathways; postmarketing requirements;<br />

the impact of regulatory differences between the U.S.<br />

and other countries; and how regulatory approval<br />

processes affect corporate strategy.<br />

Course 19007<br />

Statistical Design of Experiments:<br />

A Practical Approach<br />

The Statistical Design of Experiment (DOE) is a powerful<br />

tool for systematically analyzing factors affecting<br />

processes and their outputs, and identifying important<br />

interactions that might otherwise be missed. This<br />

methodology is applicable to a wide range of research<br />

and development experiments, as well as manufacturing,<br />

quality and marketing. It can speed up research,<br />

increase productivity, and reduce costs. Topics<br />

include screening designs, factorial designs, fractional<br />

factorials, analysis of variance, regression, response<br />

surface methods, power and sample size. Lectures and<br />

classroom DOE experiments take a practical approach,<br />

and will make use of Excel for examples and handson<br />

analyses. This course is designed for scientists<br />

and engineers working in high tech areas including<br />

biomedical research, material science, electronics and<br />

medical devices. No previous background in statistics<br />

is required.<br />

Course 23096<br />

Stem Cell Biology<br />

California is at the forefront of stem cell research and<br />

the industry continues to offer exciting opportunities<br />

in the Bay Area. This course introduces the basic<br />

biology and clinical applications of embryonic and<br />

adult stem cell therapies, provides a market overview<br />

of stem cell startup companies, and touches on the<br />

FDA regulation of biologic products.<br />

Course 13567<br />

Toxicology Basics for <strong>Biotechnology</strong><br />

Biopharmaceutical companies expend vast resources<br />

to identify new chemical and biological agents that<br />

have the potential for clinical benefit. However, before<br />

these can be tested and used widely in patients, safety<br />

and acceptable toxicity to critical organs must be<br />

demonstrated. This course surveys the adverse effects<br />

resulting from the interaction of chemical agents with<br />

living systems.<br />

Course 2310<br />

Viruses, Vaccines and Gene Therapy<br />

Interactive case studies and Web-supplemented<br />

lessons drive our exploration of the interplay of viruses<br />

with their cellular hosts. Building on these foundations,<br />

we examine salient topics in vaccines, gene<br />

therapy and therapeutic viruses. Pertinent and real<br />

issues relevant to the biopharmaceutical industry are<br />

also discussed. Course topics include virus evolution;<br />

emerging viruses—when worlds collide; the risk/<br />

benefits of vaccines; the polio eradication campaign;<br />

epidemiology of influenza; HIV-1 vaccines; and the<br />

trials and tribulations of gene therapy.<br />

Course 6974<br />

Also Recommended<br />

Data Privacy and Security<br />

for Healthcare and Biosciences<br />

Many healthcare and bioscience companies utilize<br />

Protected Health Information (PHI) or Personally<br />

Identifiable Information (PII) in order to develop and<br />

test products such as medical devices and mobile<br />

applications, or to perform other services, including<br />

data analysis on their customer’s healthcare related<br />

data. This course examines the important data privacy<br />

and security issues that govern these industries.<br />

Topics include relevant state, national and international<br />

data privacy and security regulations, medical<br />

device security and privacy, FTC requirements, HIPAA<br />

training and risk analysis requirements, among others.<br />

Not only will you understand issues relevant to your<br />

industry, but you will address these concerns by<br />

developing a plan of action toward compliance<br />

with relevant regulations and requirements.<br />

Explore <strong>UCSC</strong> <strong>Extension</strong>’s<br />

Other Bioscience Programs<br />

Bioinformatics<br />

Clinical Trials Design and Development<br />

Medical Devices<br />

Regulatory Affairs<br />

See ucsc-extension.edu/biosciences<br />

for more information.<br />

Earn Two Certificates:<br />

Learn More for Less<br />

Course 30120<br />

Students pursuing two<br />

bioscience certificates<br />

need a minimum of 30-32<br />

units (depending on the certificate), including<br />

all required courses and elective units for<br />

both programs. Please note that in order to<br />

complete two certificate programs with the<br />

minimum number of units, students must<br />

select some electives that are common to both<br />

programs.<br />

Contact us at extensionprogram@ucsc.edu<br />

or call (408) 861-3860 if you need more<br />

information or would like assistance creating<br />

a study plan.<br />

Not printed or mailed at state expense. 611791-1204-1334 (08/23/12)

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