Discover Fda Events & Activities Online

301 - FDA Insider
Tue, Jun 10, 9:00 AM EDT
301 - FDA Insider
Tue, Jun 10, 9:00 AM EDT
Sales end soon
Master FDA Inspections in 2025: Stay Compliant, Prevent Costly Setbacks
Tomorrow at 1:00 PM EDT
Sales end soon
Master FDA Inspections in 2025: Stay Compliant, Prevent Costly Setbacks
Tomorrow at 1:00 PM EDT
US FDA Formally Proposes Aligning Quality System Regulations with ISO13485.
Thursday at 1:00 PM EDT
US FDA Formally Proposes Aligning Quality System Regulations with ISO13485.
Thursday at 1:00 PM EDT
US FDA Formally Proposes Aligning Quality System Regulations with ISO 13485
Thursday at 1:00 PM EDT
US FDA Formally Proposes Aligning Quality System Regulations with ISO 13485
Thursday at 1:00 PM EDT
(TMF)- Trial Master File: FDA Expectations from Sponsors and Sites
Thu, May 15, 1:00 PM EDT
(TMF)- Trial Master File: FDA Expectations from Sponsors and Sites
Thu, May 15, 1:00 PM EDT
FDA Compliance in the Age of AI & Machine Learning
Tue, May 27, 1:00 PM GMT+5:30
FDA Compliance in the Age of AI & Machine Learning
Tue, May 27, 1:00 PM GMT+5:30
Evolution of US Drug Label Management: Leveraging Structured Product
Thu, May 15, 3:00 PM EDT
Evolution of US Drug Label Management: Leveraging Structured Product
Thu, May 15, 3:00 PM EDT
Just added!
Navigating FDA Inspections Successfully– Most Common Observation Strategies
Thu, Jun 5, 11:00 AM EDT
Just added!
Navigating FDA Inspections Successfully– Most Common Observation Strategies
Thu, Jun 5, 11:00 AM EDT
Just added!
Mastering 21 CFR 801: FDA Labeling & UDI Compliance
Thu, May 22, 1:00 PM EDT
Just added!
Mastering 21 CFR 801: FDA Labeling & UDI Compliance
Thu, May 22, 1:00 PM EDT
Achieving Maximum Benefit from Consultants
Wed, May 28, 7:00 PM EDT
Achieving Maximum Benefit from Consultants
Wed, May 28, 7:00 PM EDT
FDA Recalls - Before You Start, and After You Finish
Tue, Jul 29, 9:00 AM EDT
FDA Recalls - Before You Start, and After You Finish
Tue, Jul 29, 9:00 AM EDT
Regulatory Considerations for AI in MedTech
Thu, May 15, 12:00 PM EDT
Regulatory Considerations for AI in MedTech
Thu, May 15, 12:00 PM EDT
The 6 Most Common Problems in FDA Software Validation and Verification
Tue, May 13, 1:00 PM EDT
The 6 Most Common Problems in FDA Software Validation and Verification
Tue, May 13, 1:00 PM EDT
Mastering Design Control: Decoding Documentation for 21 CFR 820.30 and ISO
Friday at 3:00 PM EDT
Mastering Design Control: Decoding Documentation for 21 CFR 820.30 and ISO
Friday at 3:00 PM EDT
Quality Control Laboratory Compliance - cGMPs and GLPs Course
Tue, May 20, 7:00 AM EDT
Quality Control Laboratory Compliance - cGMPs and GLPs Course
Tue, May 20, 7:00 AM EDT
Sales end soon
FSMA Foreign Supplier Verification Programs (FSVP) Online Training
Thursday at 9:00 AM EDT
Sales end soon
FSMA Foreign Supplier Verification Programs (FSVP) Online Training
Thursday at 9:00 AM EDT
FSVP Course - Online Live Course - FSPCA Curriculum 1.5 Days
Thu, May 15, 8:00 AM CDT
FSVP Course - Online Live Course - FSPCA Curriculum 1.5 Days
Thu, May 15, 8:00 AM CDT
FSMA Foreign Supplier Verification Programs (FSVP) Online Training
Thu, Jun 5, 9:00 AM EDT
FSMA Foreign Supplier Verification Programs (FSVP) Online Training
Thu, Jun 5, 9:00 AM EDT
FSMA Foreign Supplier Verification Programs (FSVP) Online Training
Thu, Jul 3, 9:00 AM EDT
FSMA Foreign Supplier Verification Programs (FSVP) Online Training
Thu, Jul 3, 9:00 AM EDT
Unlocking the U.S. Market: A Guide for Italian Food & Beverage Companies
Wed, May 21, 11:00 AM EDT
Unlocking the U.S. Market: A Guide for Italian Food & Beverage Companies
Wed, May 21, 11:00 AM EDT

301 - FDA Insider

301 - FDA Insider

Master FDA Inspections in 2025: Stay Compliant, Prevent Costly Setbacks

Master FDA Inspections in 2025: Stay Compliant, Prevent Costly Setbacks

US FDA Formally Proposes Aligning Quality System Regulations with ISO13485.

US FDA Formally Proposes Aligning Quality System Regulations with ISO13485.

US FDA Formally Proposes Aligning Quality System Regulations with ISO 13485

US FDA Formally Proposes Aligning Quality System Regulations with ISO 13485

(TMF)- Trial Master File: FDA Expectations from Sponsors and Sites

(TMF)- Trial Master File: FDA Expectations from Sponsors and Sites

FDA Compliance in the Age of AI & Machine Learning

FDA Compliance in the Age of AI & Machine Learning

Evolution of US Drug Label Management: Leveraging Structured Product

Evolution of US Drug Label Management: Leveraging Structured Product

Navigating FDA Inspections Successfully– Most Common Observation Strategies

Navigating FDA Inspections Successfully– Most Common Observation Strategies

Mastering 21 CFR 801: FDA Labeling & UDI Compliance

Mastering 21 CFR 801: FDA Labeling & UDI Compliance

Achieving Maximum Benefit from Consultants

Achieving Maximum Benefit from Consultants

FDA Recalls - Before You Start, and After You Finish

FDA Recalls - Before You Start, and After You Finish

Regulatory Considerations for AI in MedTech

Regulatory Considerations for AI in MedTech

The 6 Most Common Problems in FDA Software Validation and Verification

The 6 Most Common Problems in FDA Software Validation and Verification

Mastering Design Control: Decoding Documentation for 21 CFR 820.30 and ISO

Mastering Design Control: Decoding Documentation for 21 CFR 820.30 and ISO

Quality Control Laboratory Compliance - cGMPs and GLPs Course

Quality Control Laboratory Compliance - cGMPs and GLPs Course

FSMA Foreign Supplier Verification Programs (FSVP) Online Training

FSMA Foreign Supplier Verification Programs (FSVP) Online Training

FSVP Course - Online Live Course - FSPCA Curriculum 1.5 Days

FSVP Course - Online Live Course - FSPCA Curriculum 1.5 Days

FSMA Foreign Supplier Verification Programs (FSVP) Online Training

FSMA Foreign Supplier Verification Programs (FSVP) Online Training

FSMA Foreign Supplier Verification Programs (FSVP) Online Training

FSMA Foreign Supplier Verification Programs (FSVP) Online Training

Unlocking the U.S. Market: A Guide for Italian Food & Beverage Companies

Unlocking the U.S. Market: A Guide for Italian Food & Beverage Companies

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