Trainings for FDA Compliance - Webinars, Seminars on Latest Regulations

Webinars

Statistical Justification for Using Small Sample Sizes and only 3 Lots in Process or Produ ....

John N Zorich
Mar 21, 2019

Total Organic Carbon Analysis for Cleaning Validation in Pharmaceutical Manufacturing

Joy McElroy
Mar 22, 2019

The Identification and Quantitation of low-level compounds for Impurity and Degradation An ....

John Fetzer
Mar 26, 2019

Risk Based Monitoring for GCP Compliance

Laura Brown
Mar 27, 2019

CDISC Mapping 2: ODM, MindMaps and References

Sunil Gupta
Mar 27, 2019

Managed Care Contracts and the Case Management Leader: Leading Your Department to Improved ....

Beverly Cunningham
Mar 27, 2019

Effective Records Management and Document Control for Medical Devices

Denise Wrestler
Mar 27, 2019

CMS Two Midnight Rule

Bernadette Benta
Mar 27, 2019

2019 Safe Food for Canadians Regulations

Gina Reo
Apr 2, 2019

21 CFR Part 11 and Annex 11 Compliance; Specifics for Data Integrity with SaaS/Cloud

David Nettleton
Apr 3, 2019

FDA Part 820 Basics - Everything you need to know to get your start-up Company Compliance

Denise Wrestler
Apr 3, 2019

FDA Establishment Inspections - What to Expect?

Charles H Paul
Apr 4, 2019

An Update on Discharge Planning Rules and Regulations for 2019

Toni Cesta
Apr 4, 2019

The Physician Advisor's Role in Case Management

Beverly Cunningham
Apr 4, 2019

Fair Hearings from A Hearing Officer's Perspective

William Mack Copeland
Apr 4, 2019

Neonatal Abstinence Syndrome Best Practice Management

Bernadette Benta
Apr 8, 2019

Chief Compliance Officer: What does it take to do the job? The Organization's and CCO's Re ....

Laura S Hargraves
Apr 15, 2019

ICH Q7 FDA Guidance – Its Structure, History, Application and Writer's Intent

Max Lazar
May 23, 2019

Seminars

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Webinars

Statistical Justification for Using Small Sample Sizes and only 3 Lots in Process or Produ ....

Total Organic Carbon Analysis for Cleaning Validation in Pharmaceutical Manufacturing

The Identification and Quantitation of low-level compounds for Impurity and Degradation An ....

Risk Based Monitoring for GCP Compliance

CDISC Mapping 2: ODM, MindMaps and References

Managed Care Contracts and the Case Management Leader: Leading Your Department to Improved ....

Effective Records Management and Document Control for Medical Devices

CMS Two Midnight Rule

2019 Safe Food for Canadians Regulations

21 CFR Part 11 and Annex 11 Compliance; Specifics for Data Integrity with SaaS/Cloud

FDA Part 820 Basics - Everything you need to know to get your start-up Company Compliance

FDA Establishment Inspections - What to Expect?

An Update on Discharge Planning Rules and Regulations for 2019

The Physician Advisor's Role in Case Management

Fair Hearings from A Hearing Officer's Perspective

Neonatal Abstinence Syndrome Best Practice Management

Chief Compliance Officer: What does it take to do the job? The Organization's and CCO's Re ....

ICH Q7 FDA Guidance – Its Structure, History, Application and Writer's Intent

Seminars

21 CFR Part 11 Compliance for SaaS/Cloud Applications

Computer System Validation - Reduce Costs and Avoid 483s

HIPAA Privacy Rule Compliance-Understanding New Rules and Responsibilities of Privacy Officer

Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions

Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina)

FDA Recalls - Before You Start, and After You Finish

Managing Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an Inspection

FDA's GMP Expectations for Phase I and First-in-Man Clinical Trials

REACH and RoHS Compliance: Gain a Deeper Understanding

FDA's New Import Program for 2019 - Strict Precision

Effective Quality Oversight of Pharmaceutical Contract Manufacturing Organizations (CMOs)

Quality Control Laboratory Compliance - cGMPs and GLPs

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