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FDA's Emerging Signals Guidance: Reporting Medical Device Safety Warnings

Susanne Manz

Recorded Duration : 60 Minutes

Life Sciences > Medical Device | Diagnostic | Pharmaceutical | Biologics fields

Susanne Manz, MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma. She has an extensive background ...

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GAMP® 5 System Classification and Compliance for Computer Systems Regulated by FDA

Carolyn Troiano

Recorded Duration : 90 Minutes

Life Sciences > Medical Device | Diagnostic | Pharmaceutical | Biologics fields

Carolyn Troiano has more than 30 years of experience in computer system validation in the pharmaceutical, medical device, animal health, tobacco and other FDA-regulated indust...

Webinar

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GAMP® 5 System Classification and Compliance for Computer Systems Regulated by FDA

Carolyn Troiano

Recorded Duration : 90 Minutes

Life Sciences > Medical Device | Diagnostic | Pharmaceutical | Biologics fields

Carolyn Troiano has more than 30 years of experience in computer system validation in the pharmaceutical, medical device, animal health, tobacco and other FDA-regulated indust...

Webinar

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CMO Supplier Quality Agreements - Comply with new FDA & EU GMP Guidelines for Contract Drug Manufact...

Recorded Duration : 60 Minutes

Life Sciences > Pharmaceutical

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6-hr Virtual Seminar: Understanding Corrective and Preventive Action in FDA- and ISO-Regulated Indus...

Jeff Kasoff

Recorded Duration : 360 Minutes

Life Sciences > Medical Device | Diagnostic | Pharmaceutical | Biologics fields

Jeff Kasoff, RAC, CMQ/OE, Lean Black Belt, has more than 30 years in Quality and Regulatory management. Over that time, Jeff has implemented and overseen quality system operat...

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Complaint Handling in Compliance with FDA and ISO Regulations

Jeff Kasoff

Recorded Duration : 60 Minutes

Life Sciences > Medical Device | Diagnostic | Pharmaceutical | Biologics fields

Jeff Kasoff, RAC, CMQ/OE, Lean Black Belt, has more than 30 years in Quality and Regulatory management. Over that time, Jeff has implemented and overseen quality system operat...

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3-hr Virtual Seminar: Technical Writing for the Pharmaceutical, Medical Device and Biotech Industrie...

Joy L. McElroy

Recorded Duration : 90 Minutes

Life Sciences > Biotechnology

Joy McElroy entered the pharmaceutical industry in 1992 shortly after earning a Bachelor of Science degree at North Carolina State University. ...

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2-hr Virtual Seminar: FDA Inspections - Understanding the Core Elements

LIVE : May 20 , 2024 01:00 PM EDT

21 CFR 58 - Good Laboratory Practice (GLP) and USP 1058 Validations

John E. Lincoln

LIVE : May 30 , 2024 01:00 PM EDT

6-Hour Virtual Seminar - Death by CAPA - Does your CAPA Program need a CAPA?

Susanne Manz

LIVE : June 18 , 2024 11:00 AM EDT

6-Hour Virtual Seminar on 21 CFR Part 11 Compliance for Computer Systems Regulated by FDA

Carolyn Troiano

LIVE : June 19 , 2024 11:00 AM EDT

6-hr Virtual Seminar: Medical Device Regulations and Evolving Requirements: Post Market Surveillance...

LIVE : June 25 , 2024 11:00 AM EDT

FDA's Emerging Signals Guidance: Reporting Medical Device Safety Warnings

Susanne Manz

Recorded Duration : 60 Minutes

GAMP® 5 System Classification and Compliance for Computer Systems Regulated by FDA

Carolyn Troiano

Recorded Duration : 90 Minutes

GAMP® 5 System Classification and Compliance for Computer Systems Regulated by FDA

Carolyn Troiano

Recorded Duration : 90 Minutes

CMO Supplier Quality Agreements - Comply with new FDA & EU GMP Guidelines for Contract Drug Manufact...

Recorded Duration : 60 Minutes

6-hr Virtual Seminar: Understanding Corrective and Preventive Action in FDA- and ISO-Regulated Indus...

Jeff Kasoff

Recorded Duration : 360 Minutes

Complaint Handling in Compliance with FDA and ISO Regulations

Jeff Kasoff

Recorded Duration : 60 Minutes

3-hr Virtual Seminar: Technical Writing for the Pharmaceutical, Medical Device and Biotech Industrie...

Joy L. McElroy

Recorded Duration : 90 Minutes

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