CRN
30515
Term
Spring 2025
Subject
Course
12A
Section
651
Catalog Description

A general overview of Food and Drug Administration regulations as they pertain to the biotechnology field. Knowledge of Current Good Laboratory Practices (cGLP) and Current Good Manufacturing Practices (cGMP) is needed to work in biotechnology manufacturing and preclinical research laboratories. The course will emphasize those practices as they pertain to the biopharmaceutical industry.

Section Notes

BTEC 12A meets in person and requires the use of Canvas. All coursework is completed on Canvas using an internet enabled device.

Requisites

Recommended Preparation, ESL 186 or placement in ESL 188 or readiness for college-level English

Learning Outcomes