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Live Online Courses - given online, at a prescheduled time, by a live instructor
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Online courses are currently being transitioned to a new learning management system, and are temporarily unavailable.

Live Online

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Note: All course information is presented in Eastern Time.

Core Concepts of Biomanufacturing and Quality Systems (March 17-18, 2022, 9:00am-5:00pm)

Core Concepts of Biomanufacturing and Quality Systems (CCB)

March 17-18, 2022
9:00am-5:00pm ET

Price:

Total Cost - Live Courses

Core Concepts of Biomanufacturing and Quality Systems (CCB)

March 17-18, 2022
9:00am-5:00pm ET

Price:

Total Cost - Live Courses

Live Online Course Selection

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Please note that each course consists of ~2 hours of instruction, plus 1 hour for the course assessment.

New Course Offerings Coming Soon!

cGLP for Nonclinical Laboratory Studies: Select Course Date*

Note: All courses take place 1:00 - 4:00 pm ET

Thursday, May 26, 2022

Navigating the Pre-IND Pathway: Select Course Date*

Note: All courses take place 1:00 - 4:00 pm ET

Thursday, April 28, 2022

cGMP for Biopharmaceutical Drug Products: Select Course Date*

Note: All courses take place 1:00 - 4:00 pm ET

Friday, May 13, 2022

Tuesday, June 28, 2022

Certificate Short Course - Live Online

cGMP for (Bio)Pharmaceuticals

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Certificate Short Course - Live Online

cGLP for Nonclinical Laboratory Studies

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Certificate Short Course - Live Online

Navigating the Pre-IND Pathway

Price:

Total Cost - Live Online Courses

Certificate Short Course

cGMP for (Bio)Pharmaceuticals

Price:

Certificate Short Course

cGLP for Nonclinical Laboratory Studies

Price:

Certificate Short Course

Navigating the Pre-IND Pathway

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Live Online Course(s) Total

Online Course Selection

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cGMP for Dietary Supplements

Corrective Action Preventive Action

Good Documentation Practices

Basics of Project Management

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Bloodborne Pathogens

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cGMP for (Bio)Pharmaceuticals

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cGMP for Dietary Supplements

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cGMP for Medical Devices

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Chemical Hygiene Plans

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Corrective Action Preventive Action

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Environmental Monitoring

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Equipment Qualification

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FDA Labeling Regulations

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Good Documentation Practices

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Guide to FDA Warning Letters

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Inventory Management

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Medical Device Design Controls

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Process Validation

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Quality Audits

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Regulatory Approval for Medical Devices

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The 5 Pillar Strategy for a Lean Workplace

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Writing Controlled Documents

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