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Showing 641-650 of 692 items.

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Implementing a Modern Quality Risk Management

Steven Laurenz

Recorded Duration : 60 Minutes

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

Steven Laurenz has over 25 years of technical leadership experience in product development, process development, technology transfer, and process optimization. He is skilled i...

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Analyzing Assay Validation for Clinical Diagnostics

Todd Graham

Recorded Duration : 60 Minutes

Life Sciences > Clinical | Biotechnology | Laboratory

Todd Graham , is a masters-level bench scientist and medical technologist with a host of experience in both the clinical diagnostics and biotechnology fields. He has work for ...

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Patients' Medical Records: Disposition of Records and Records Retention, Including Electronic Record...

Mark Brengleman

Recorded Duration : 60 Minutes

Life Sciences > Healthcare

Mark worked as the assigned counsel to numerous health professions licensure boards as an Assistant Attorney General for the Commonwealth of Kentucky. Moving to private practi...

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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...

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GMP Auditing of Facilities Performing Cell-Based Methods

Gwendolyn Wise-Blackman

Recorded Duration : 60 Minutes

Life Sciences > Pharmaceutical

Gwen Wise-Blackman has 20 years of combined experience in Cell-Based Assays and Quality Systems. She has worked at DuPont Pharmaceuticals, Catalent Pharma Solutions (formerly ...

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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...

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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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How to Manage OCR, HHS HIPAA and HITECH Audit

Srini Kolathur

Recorded Duration : 60 Minutes

Life Sciences > Healthcare

Srini Kolathur, HITPro, CISSP,CISA, CISM, MBA is a result-driven leader. Srini has several years of experience in helping companies effectively meet and exceed regulatory comp...

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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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Recorded

Problem Solving - Root Cause Analysis in Pharma Manufacturing

Joy L. McElroy

LIVE : November 26 , 2024 01:00 PM EST

Essentials of Validation – IQ, OQ, PQ

LIVE : November 27 , 2024 01:00 PM EST

Implementing a Modern Quality Risk Management

Steven Laurenz

Recorded Duration : 60 Minutes

Analyzing Assay Validation for Clinical Diagnostics

Todd Graham

Recorded Duration : 60 Minutes

Patients' Medical Records: Disposition of Records and Records Retention, Including Electronic Record...

Mark Brengleman

Recorded Duration : 60 Minutes

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

GMP Auditing of Facilities Performing Cell-Based Methods

Gwendolyn Wise-Blackman

Recorded Duration : 60 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

How to Manage OCR, HHS HIPAA and HITECH Audit

Srini Kolathur

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

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