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Life Sciences

Understand dynamic regulatory environment in the life sciences industry. Find courses covering a wide variety of topics, including Good Manufacturing Practices (GMP), quality assurance, Contamination control, development and approval, immunogenicity testing, Good laboratory practices (GLP), Medical Device Reporting (MDR), computer system validation, packaging and labeling regulations, clinical trial audit, FSMA, and more.

Webinar

Clinical Trial

Responding to Clinical Observations: Developing Robust Audit & Insp...
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Jan 20, 2022 - 01:00 PM EST
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Webinar

Clinical Trial

The Importance Of Protocol Deviations and Violations to Subject Saf...
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Jan 24, 2022 - 03:00 PM EDT
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Webinar

Hospital & Healthc..

Grievances and Complaints: Ensuring Hospitals Compliance with the C...
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Jan 26, 2022 - 01:00 PM EDT
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Webinar

Clinical Trial

Management of the Data Safety Management Committee for Clinical Trials
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Jan 26, 2022 - 01:00 PM EDT
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Webinar

Medical Devices

Complaint Handling Requirements (US); Interrelationship with CAPA, ...
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Jan 27, 2022 - 03:00 PM EST
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Webinar

Clinical Trial

Standard Operating Procedures for Risk-Based Monitoring of Clinica...
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Jan 27, 2022 - 01:00 PM
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Recorded

Hospital & Healthc..

Grievances and Complaints: Ensuring Hospitals Compliance with the C...
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Price: $ 449
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Recorded

Hospital & Healthc..

The Complexity and Interplay Among ADAAA, FMLA, and Worker's Comp (...
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Price: $ 349
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Recorded

Food Safety & Diet..

Managing Data and Documentation for FDA Inspections
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Price: $ 349
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Recorded

Medical Devices

Process Verification and Validation Planning and Execution
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Price: $ 249
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Recorded

Pharmaceutical

21 CFR Part 11 and QMS Software Risk-Based Implementation
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Price: $ 349
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