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Showing 171-180 of 703 items.

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3 Hours Virtual Seminar on 21 CFR Part 11 Guidance for Electronic Records and Electronic Signatures ...

Carolyn Troiano

Recorded Duration : 180 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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Technical Writing for a Traditional 510(k) Submission

John E. Lincoln

Recorded Duration : 90 Minutes

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

John E. Lincoln, is Principal of J. E. Lincoln and Associates LLC, a consulting company with over 38 years experience in U.S. FDA-regulated ind...

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The End of the Public Health Emergency is Near: What Your Health Care Organization Needs to do Now?

Joseph Wolfe

Recorded Duration : 60 Minutes

Life Sciences > Healthcare

Joseph Wolfe is an attorney with Hall Render, the largest healthcare-focused law firm in the country. Mr. Wolfe supports high-performing hospitals, health systems, medical gro...

Webinar

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3-hr Virtual Seminar on IEC 62304 and Demystifying Software Validation

Jose Mora

Recorded Duration : 180 Minutes

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

Jose Mora, is a Principal Consultant specializing in Manufacturing Engineering and Quality Systems. For over 30 years he has worked in the medical device and life sciences ind...

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How to Prepare a 510(k) Submission

Edwin Waldbusser

Recorded Duration : 60 Minutes

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

Ed retired from industry after 30 years in management of development of medical device products and development of company Quality Systems. He was involved in the development ...

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3-Hour Virtual Seminar: Effective Cleaning Validation Procedures

Joy L. McElroy

Recorded Duration : 180 Minutes

Life Sciences > Pharmaceutical | Biotechnology | Clinical | Laboratory

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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Regulatory Requirements for Conducting an OOS Investigation

Danielle DeLucy

Recorded Duration : 60 Minutes

Life Sciences > Pharmaceutical | Biotechnology | Clinical | Laboratory

Danielle DeLucy, MS, is owner of ASA Training and Consulting, LLC which provides Pharmaceutical and Biologics based companies with training and quality systems assistance in o...

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Documentation Needs: Medical Device Software per IEC 62304

Jose Mora

Recorded Duration : 60 Minutes

Life Sciences > Medical Devices

Jose Mora, is a Principal Consultant specializing in Manufacturing Engineering and Quality Systems. For over 30 years he has worked in the medical device and life sciences ind...

Webinar

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Drafting and Negotiating Physician Employment Agreements: Key Considerations for 2023

Joseph Wolfe

Recorded Duration : 60 Minutes

Life Sciences > Healthcare | Clinical | Laboratory

Joseph Wolfe is an attorney with Hall Render, the largest healthcare-focused law firm in the country. Mr. Wolfe supports high-performing hospitals, health systems, medical gro...

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GMP Auditing for Pharmaceutical Manufacturing

Carl Patterson, MS, SSGB, SSBB

Recorded Duration : 60 Minutes

Life Sciences > Pharmaceutical | Biotchnology | Laboratory

Carl Patterson is a seasoned Pharmaceutical Manufacturing, Aseptic Processing, and Quality Assurance professional who is based in San Diego, Ca...

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Recorded

Essentials of Validation – IQ, OQ, PQ

LIVE : April 08 , 2025 01:00 PM EST

21 CFR Part 820 - Quality System Regulation - Principles of Lean Documents and Lean Configuration

Jose Mora

LIVE : April 09 , 2025 01:00 PM EST

3 Hours Virtual Seminar on 21 CFR Part 11 Guidance for Electronic Records and Electronic Signatures ...

Carolyn Troiano

Recorded Duration : 180 Minutes

Technical Writing for a Traditional 510(k) Submission

John E. Lincoln

Recorded Duration : 90 Minutes

The End of the Public Health Emergency is Near: What Your Health Care Organization Needs to do Now?

Joseph Wolfe

Recorded Duration : 60 Minutes

3-hr Virtual Seminar on IEC 62304 and Demystifying Software Validation

Jose Mora

Recorded Duration : 180 Minutes

How to Prepare a 510(k) Submission

Edwin Waldbusser

Recorded Duration : 60 Minutes

3-Hour Virtual Seminar: Effective Cleaning Validation Procedures

Joy L. McElroy

Recorded Duration : 180 Minutes

Regulatory Requirements for Conducting an OOS Investigation

Danielle DeLucy

Recorded Duration : 60 Minutes

Documentation Needs: Medical Device Software per IEC 62304

Jose Mora

Recorded Duration : 60 Minutes

Drafting and Negotiating Physician Employment Agreements: Key Considerations for 2023

Joseph Wolfe

Recorded Duration : 60 Minutes

GMP Auditing for Pharmaceutical Manufacturing

Carl Patterson, MS, SSGB, SSBB

Recorded Duration : 60 Minutes

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