Help and Support Request a callback Toll Free : 1-888-844-8963   Fax : 347-719-4399
  1. Home

Your Search Result For All Webinars

Showing 1-4 of 4 items.
Webinar
View Details
Good Documentation Guideline (Chapter <1029> USP)
Dr. Afsaneh Motamed Khorasani
LIVE : October 16 , 2025 01:00 PM EDT
Life Sciences > Pharmaceutical | Biotchnology | Laboratory

Dr. Afsaneh Motamed Khorasani, PhD, is a Medical and scientific Affairs expert and a Senior Scientist with a strong background in biomedical sc...

Webinar
View Details
How to Prepare For and Host a FDA Inspection and Respond to 483’s
Edwin Waldbusser
LIVE : October 16 , 2025 01:00 PM EDT
Life Sciences > Medical Devices
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 ...
Webinar
View Details
2-hr Virtual Seminar: FDA Inspections - Understanding the Core Elements
LIVE : October 22 , 2025 01:00 PM EDT
Life Sciences > Medical Device | Diagnostic | Pharmaceutical | Biologics fields
Webinar
View Details
Essentials of Validation – IQ, OQ, PQ
LIVE : October 23 , 2025 01:00 PM EDT
Life Sciences > Medical Devices
Showing 351-360 of 702 items.
Webinar
View Details
FMEA and Fault Tree Analysis for Preventing Hospital Risks
Dev Raheja
Recorded Duration : 90 Minutes
Life Sciences > Healthcare
Dev Raheja, MS,CSP, is an international Risk Management and Quality Assurance consultant for Healthcare,medical device, and aerospace industry for over 25 years. He applies ev...
Webinar
View Details
Clinical Trial Master File Compliance
Carolyn Troiano
Recorded Duration : 90 Minutes
Life Sciences > Clinical | Biotechnology | Laboratory
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
View Details
In Depth Testing of 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
View Details
GxP/GMP Requirements and its Consequences for Documentation and Information Technology Systems
Eleonora Babayants
Recorded Duration : 90 Minutes
Life Sciences > Pharmaceutical | Biotechnology | Clinical | Laboratory

Galaxy Consulting Founder and President Eleonora Babayants is a documentation management professional and hands-on consultant with over 25 year...

Webinar
View Details
Risk and Its Impact on Medical Device Design
Charles H. Paul
Recorded Duration : 90 Minutes
Life Sciences > Medical Devices
Charles H. Paul is the President of C. H. Paul Consulting, Inc. – a regulatory, training, and technical documentation consulting firm. Charles is a management consultant...
Webinar
View Details
EPA Final Rule for Hazardous Waste Pharmaceuticals and Nicotine Exemption
Dr. Marge McFarlane, PhD, MT (ASCP), CHFM, CJCP, CHSP, HEM, MEP
Recorded Duration : 60 Minutes
Life Sciences > Healthcare | Clinical | Pharmaceuticals

Marge McFarlane, PhD, MT (ASCP), CHFM, CJCP, CHSP, HEM, MEP, brings over 40 years of comprehensive experience in the environment of care, life ...

Webinar
View Details
QSR-Compliant Equipment Control & Validation of Processes in the Manufacturing Environment
Joy L. McElroy
Recorded Duration : 75 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. ...

Webinar
View Details
Effective and Compliant Failure Investigations and writing CAPA
Joy L. McElroy
Recorded Duration : 90 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. ...

Webinar
View Details
Essential Regulatory Documents and Regulatory Requirements for Biomedical Products
Marina Malikova
Recorded Duration : 90 Minutes
Life Sciences > Pharmaceutical | Biotechnology | Clinical | Laboratory

Dr. Malikova has over twenty years of experience in the clinical research field. She has managed Phase I – IV studies involving investiga...

Webinar
View Details
Risk-Based Quality and Compliance Management in Clinical Trials with Combination Products
Marina Malikova
Recorded Duration : 90 Minutes
Life Sciences > Clinical | Biotechnology | Laboratory

Dr. Malikova has over twenty years of experience in the clinical research field. She has managed Phase I – IV studies involving investiga...

live

LIVE

photos0

CART

About Us Refund Policy Terms of Services Privacy Policy Contact Us Speaking Opportunity Blog Careers Unsubscribe