Corrective Action Preventive Action (CAPA)
COURSE DESCRIPTION CAPA… the word strikes fear in the hearts of some, dread in the hearts of others. But the truth is that CAPAs…
Guide to FDA Warning Letters
COURSE DESCRIPTION The outcome of regulatory inspections is critical to an organization’s success. If the outcome of the inspection results in FDA 483 observations…
Inventory Management
COURSE DESCRIPTION Inventory is expensive and difficult to manage, and yet is an essential requirement for providing great service to customers. This course provides…
The 5 Pillar Strategy for a Lean Workplace
This course provides future or current employees a comprehensive and applied understanding of how regulatory compliance is built into all aspects of a company.
BACE Open Testing
DESCRIPTION Launched in 2012, the BACE assesses the skills and knowledge valued by the bioscience industry. Exam questions are written and validated by subject-matter…
Know your ABCs: Applications of Biotechnology for the Classroom
COURSE DESCRIPTION This week-long (40-hour) program is designed for educators who are (or will be) teaching Biotechnology courses, Project Lead the Way’s Biomedical Science…
Introduction to Clinical Research
COURSE DESCRIPTION This course will provide an overview of the Clinical Research industry, to include a description of who the major players are and…
Regulatory Approval for Medical Devices
COURSE DESCRIPTION The Food and Drug Administration is responsible for ensuring that medical devices are safe and effective for their intended uses before they…
Medical Device cGMPs Internationally
COURSE DESCRIPTION Good manufacturing practices are a set of principles and procedures that help ensure medical devices are manufactured with the required quality. In…
Corrective and Preventive Action (CAPA) for the Medical Device Industry
COURSE DESCRIPTION Good manufacturing practices are the regulations enforced by the United States Food and Drug Administration (FDA) for medical devices. Part of these…
Process Validation
COURSE DESCRIPTION Good manufacturing practices are the regulations enforced by the United States Food and Drug Administration (FDA) for medical devices. These regulations provide…
Quality Audits
COURSE DESCRIPTION Medical Devices are marketed globally via country specific regulatory approval processes. These processes involve strict adherence and compliance with regulatory requirements and…
HVAC Cleanroom Design Concepts for Pharmaceutical Compounding
COURSE DESCRIPTION Taught by an expert in cleanroom design, this course will focus on the revised standards governing pharmaceutical compounding facilities set forth by…
Cleanrooms and Gowning
Gain practical experience within this critical aspect of Current Good Manufacturing Practices.
Core Concepts in Biomanufacturing and Quality Systems: Applications of cGMPs
This course provides future or current employees a comprehensive and applied understanding of how regulatory compliance is built into all aspects of a company.
Current Good Manufacturing Practices (cGMPs) for Dietary Supplements
In this course, We’ll learn how to create websites by structuring and styling your pages with HTML and CSS.
Current Good Manufacturing Practices for Medical Devices
Good manufacturing practices are the regulations enforced by the United States Food and Drug Administration (FDA) for medical devices. They are often referred to…
BACE Administrator Workshop
COURSE DESCRIPTION Biotility at UF’s Center of Excellence for Regenerative Health Biotechnology (UF CERHB) invites you to a hands-on workshop on administering the Biotechnician…
Basics of Bioinformatics
COURSE DESCRIPTION This course provides an opportunity to learn and apply the fundamentals of bioinformatics and molecular modeling techniques using the specialized app Molecular…
Industrial Biotechnology Teacher Experience (IBTE)
COURSE DESCRIPTION IBTE is a two week, 80-hour program developed for educators who are (or will be) teaching Biotechnology courses*, Project Lead the Way’s…
Elements of a GMP-Compliant Quality Control Laboratory
Practical examples, case studies and hands-on activities will be used to illustrate FDA QC laboratory hot button issues and regulatory compliance as related to…
Environmental Monitoring in a (Bio)Pharmaceutical Manufacturing Facility
Participants in this course will be introduced to the principles of environmental monitoring including hands-on activities.
Good Documentation Practices (GDPs) in a cGMP Environment
Participants in this course will learn the history of GDPs, strategies for implementing compliance, as well as standards and practices for accurately completing cGMP…
Good Documentation Practices and Quality Assurance
Lorem Ipsum is simply dummy text of the printing and typesetting industry. Lorem Ipsum has been the industry’s standard dummy text ever since the…
