Trainings for FDA Compliance - Webinars, Seminars on Latest Regulations

Webinars

Best Practices for an Effective Cleaning Validation Program

Joy McElroy
Nov 19, 2019

How to Prepare a Standard Operating Procedure (SOP)?

Afsaneh Motamed Khorasani
Nov 19, 2019

Complaint Handling Requirements (US); Interrelationship with CAPA, Change Control, Adverse ....

Vanessa Lopez
Nov 19, 2019

You have a BI Positive or Product Sterility Positive - Now What?

Gerry O Dell
Nov 19, 2019

GxP/GMP Requirements and its Consequences for Documentation and Information Technology Sys ....

Eleonora Babayants
Nov 20, 2019

Validation Master Plan - The Unwritten Requirements

John E Lincoln
Nov 20, 2019

EU IVDR 2017/746 - the new EU regulation for invitro diagnostic

Frank Stein
Nov 20, 2019

Human Error and Cognitive Load: How to Reduce Memory and Attention Failures

Ginette M Collazo
Nov 25, 2019

Post Market Surveillance with the new Medical Device Regulation EU MDR 745/2017

Frank Stein
Nov 26, 2019

Recognizing and Responding to "Red Flags" in Clinical Operations

Peggy Berry
Dec 11, 2019

ISO 13485:2016 - What are the hot topics and changes?

Frank Stein
Dec 13, 2019

Data Blocking and Patient Access of Medical Records under HIPAA - New Focus of Enforcement ....

Jim Sheldon-Dean
Dec 17, 2019

HIPAA Audits and Enforcement for 2019 - Current Issues and Focus for HIPAA Compliance

Jim Sheldon-Dean
Jan 7, 2020

Seminars

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Webinars

Best Practices for an Effective Cleaning Validation Program

How to Prepare a Standard Operating Procedure (SOP)?

Complaint Handling Requirements (US); Interrelationship with CAPA, Change Control, Adverse ....

You have a BI Positive or Product Sterility Positive - Now What?

GxP/GMP Requirements and its Consequences for Documentation and Information Technology Sys ....

Validation Master Plan - The Unwritten Requirements

EU IVDR 2017/746 - the new EU regulation for invitro diagnostic

Human Error and Cognitive Load: How to Reduce Memory and Attention Failures

Post Market Surveillance with the new Medical Device Regulation EU MDR 745/2017

Recognizing and Responding to "Red Flags" in Clinical Operations

ISO 13485:2016 - What are the hot topics and changes?

Data Blocking and Patient Access of Medical Records under HIPAA - New Focus of Enforcement ....

HIPAA Audits and Enforcement for 2019 - Current Issues and Focus for HIPAA Compliance

Seminars

Quality Control Laboratory Compliance - cGMPs and GLPs

Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR

Biocompatibility Testing for Medical Devices

Preparing for FDA's New Import/Export Trauma in 2020

Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices

REACH and RoHS Compliance: Gain a Deeper Understanding

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

Designing and Sustaining New and Existing Product Stability Testing Program

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

FDA Recalls - Before You Start, and After You Finish

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