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Life Sciences Regulations Training, Compliance Best Practices and Standards
Life science product regulations based webinars, in-person seminars, standards and best practices. Learn from renowned experts about FDA and global regulations for life science products – FDA GMP, FDA GCP, FDA GLP, FDA Submission Guidelines, Food Safety, FDA packaging and labeling guidelines, Life science product regulations in Latin America, China, South Korea, etc.Sub Categories:
Drugs and Chemicals (Pharma)
|
Medical Devices
|
Clinical Research
|
Biotechnology
|
All FDA Regulated Industry
|
Laboratory

Webinar
7
/ May
Wednesday-2025
Data Integrity and Privacy: Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR
- Speaker: David Nettleton
- Product ID: 701687
- Duration: 90 Min
* Per Attendee
$229
$229
Webinar

19
/ May
Monday-2025
Performing Effective Management Review of the Quality System
- Speaker: David L Chesney
- Product ID: 704933
- Duration: 90 Min
* Per Attendee
$199
$199
Webinar

22
/ May
Thursday-2025
Annual Current Good Manufacturing Practices (cGMP) Training
- Speaker: Kelly Thomas
- Product ID: 705422
- Duration: 60 Min
* Per Attendee
$199
$199
Webinar

22
/ May
Thursday-2025
How to Investigate Environmental Monitoring Excursions
- Speaker: Gerry O Dell
- Product ID: 701354
- Duration: 90 Min
* Per Attendee
$199
$199
Webinar

9
/ Jun
Monday-2025
Effective Systems for Change Control in the Pharmaceutical Industry
- Speaker: David L Chesney
- Product ID: 705002
- Duration: 90 mins
* Per Attendee
$199
$199
Seminar

Latin America: Understanding Regulatory Compliance Requirements Across the Life Science Industry (Pharmaceuticals, Biologics, Medical Devices, IVDs)
Location: Virtual Seminar | April 25, 2025
Robert J. Russell
President and CEO, RJR Consulting, Inc.
* For one Registration
$449
Seminar

21 CFR Part 11 Compliance for SaaS/Cloud Applications
Location: Virtual Seminar | June 25-26, 2025
David Nettleton
FDA Compliance Specialist, Computer System Validation
* For one Registration
$1499
Seminar

Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR
Location: Virtual Seminar | June 25-26, 2025
David Nettleton
FDA Compliance Specialist, Computer System Validation
* For one Registration
$1499
Seminar

Managing GMP Compliance and Phase Appropriate GMP Considerations for Virtual Companies
Simu Live
On-demand Streaming - Virtual Training Through WebEx
On-demand Streaming - Virtual Training Through WebEx
David L. Chesney
Principal and General Manager, DL Chesney Consulting, LLC (Former FDA Director)
* For one Registration
$1199
Seminar

Change Control Best Practices - Avoiding Unintended Consequences of Changes
Simu Live
On-demand Streaming - Virtual Training Through WebEx
On-demand Streaming - Virtual Training Through WebEx
Michael Ferrante
President, Quality and Compliance Associates LLC
* For one Registration
$1099
Seminar

Effective Quality Oversight of Pharmaceutical Contract Manufacturing Organizations (CMOs)
Simu Live
On-demand Streaming - Virtual Training Through WebEx
On-demand Streaming - Virtual Training Through WebEx
Michael Ferrante
President, Quality and Compliance Associates LLC
* For one Registration
$1099
Recorded/CD

Total Organic Carbon Analysis for Cleaning Validation in Pharmaceutical Manufacturing
- Speaker: Joy McElroy
- Product ID: 705929
- Duration: 90 mins
CD/Recorded
$199
$199
Recorded/CD

Designing an Effective Cleaning Validation for Reusable Medical Devices in Today's Regulatory Environment
- Speaker: Gerry O Dell
- Product ID: 701929
- Duration: 90 Min
CD/Recorded
$249
$249
Recorded/CD

You have a BI Positive or Product Sterility Positive - Now What?
- Speaker: Gerry O Dell
- Product ID: 703288
- Duration: 75 Min
CD/Recorded
$249
$249
Recorded/CD

Sterile Filtration of Pharmaceutical Products - Validation and Regulatory Requirements
- Speaker: Roger Cowan
- Product ID: 703727
- Duration: 60 Min
CD/Recorded
$249
$249

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