Pharma Guidelines, Pharma Conferences and Training Program.

Date

Conference

Speaker

Price

May 25, 2023

GMP For QC Laboratory Compliance

Ms. Kelly Thomas

$199

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Apr 26, 2023

FDA 483s, Warning Letters And Enforcement Trends

Ms. Kelly Thomas

$199

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Apr 20, 2023

The FDA recently released a new draft guidance related to Part 11

Carolyn Troiano

$199

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Mar 31, 2021

Human Error Reduction in GMP Related Environments

Ginette Collazo

$199

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Mar 24, 2021

Successful Supplier Audits

Danielle DeLucy

$199

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Aug 27, 2020

2020 CARES Act & OTC Drug Reform

Norma Skolnik

$199

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Aug 06, 2020

FDA Regulation of Artificial Intelligence/ Machine Learning

Edwin Waldbusser

$199

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Mar 04, 2020

Risk-Based Verification and Validation Planning to Meet US FDA and ISO 13485 Requirements

John E. Lincoln

$249

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Feb 26, 2020

Final Rule: Management Standards for Hazardous Waste Pharmaceuticals

Charlotte Smith

$249

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Feb 19, 2020

Medical Device Software Validation Meeting FDA Regulations

Edwin Waldbusser

$249

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Jan 14, 2020

FDA’s Cloud Compliance & Regulations

Angela Bazigos

$249

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Oct 07, 2019

Establishing Appropriate Quality Metrics and Key Performance Indicators (KPIs)

Ms. Kelly Thomas

$249

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Jun 26, 2019

FDA 21 CFR Part 11 - Electronic Records and Electronic Signatures

Carolyn Troiano

$249

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Jun 25, 2019

OSHA Guidelines on Workplace Violence & Active Shooter Scenarios

Joe Keenan

$249

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May 29, 2019

Compliant Qualification of Contract Manufacturing Organizations (CMOs)

Edwin Waldbusser

$249

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May 16, 2019

How to Satisfy OSHA Requirements and ADA Obligations 101

Joe Keenan

$249

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May 09, 2019

Proposition 65: All About California’s Supply Chain Risk Regulation

Travis Miller

$229

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May 02, 2019

The FDA Inspection Process: From SOP to 483

Richard Chamberlain

$249

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Mar 26, 2019

Navigating the New OSHA 300 Log Electronic Reporting System Before 2019 Deadline

Joe Keenan

$249

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Mar 12, 2019

Steam Sterilization Microbiology and Autoclave Performance Qualification

Danielle DeLucy

$229

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Feb 26, 2019

Navigating the New OSHA 300 Log Electronic Reporting System Before 2019 Deadline

Joe Keenan

$249

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Jan 29, 2019

Establishing Appropriate Quality Metrics and Key Performance Indicators (KPIs)

Ms. Kelly Thomas

$699

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Dec 17, 2018

OSHA Law Update 2018: Conducting OSHA 300 Log Record-keeping Training

Joe Keenan

$249

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Dec 12, 2018

2018 Update: Overview of Recent Medical Device Regulatory Changes in China

John Balzano

$249

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Nov 20, 2018

Best Practices in CAPA Management and Root Cause Analysis

Danielle DeLucy

$249

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Nov 16, 2018

Preparing a 510(k) Submission That Meets All FDA Requirements

Edwin Waldbusser

$249

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Nov 15, 2018

Human Error Prevention in Pharmaceutical Manufacturing

Charles H. Paul

$249

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Oct 29, 2018

FDA’s Expectations from Supplier Management for GMP: Quality Agreements and More

Danielle DeLucy

$249

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Oct 26, 2018

Classifying Medical Devices as per FDA Regulations

Charles H. Paul

$249

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Oct 25, 2018

Mobile Medical Apps (Is It an FDA Regulated Device) and Cybersecurity

Edwin Waldbusser

$249

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Oct 24, 2018

Management of Standard Operating Procedures

Richard Chamberlain

$229

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Oct 18, 2018

OSHA Law Update 2018: Conducting OSHA 300 Log Record-keeping Training

Joe Keenan

$249

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Oct 15, 2018

Developing a Strategic Approach to FDA Compliance for Computer System Validation

Carolyn Troiano

$249

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Oct 08, 2018

Medical Device Industry Trends for Computer Systems Regulated by FDA

Carolyn Troiano

$249

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Oct 03, 2018

Best Practices for Investigating Deviations Write-Ups and Management

Danielle DeLucy

$249

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Sep 19, 2018

Electronic Records and Signatures - 21 CFR Part 11: Basic Concepts

Angela Bazigos

$249

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Sep 14, 2018

3 Hour Boot Camp: Sharps Safety Program: Risks, Legal Concerns, Prevention & Management of Sharps Injuries

Angela Bazigos

$349

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Sep 05, 2018

FDA Case Scenarios – Best Practices for Managing Inspection Situations

Danielle DeLucy

$249

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Aug 29, 2018

Best Practices to Prepare for an FDA Computer System Audit

Carolyn Troiano

$249

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Aug 24, 2018

Customs-Trade Partnership Against Terrorism (C-TPAT) Compliance for Regulated Industries

Carolyn Troiano

$249

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Aug 01, 2018

Responding to FDA 483s and FDA Warning Letters - Can you afford not to be prepared?

Angela Bazigos

$699

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Jul 30, 2018

Sunshine Act Reporting – Clarification for Clinical Research

Danielle DeLucy

$249

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Jul 24, 2018

Prevent Workplace Violence and Meet OSHA Standards

Joe Keenan

$229

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Jul 10, 2018

OSHA 101 - OSHA Standards to Know Inside and Out

Natalia Olive

$229

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Jun 27, 2018

Effective Batch Record Review

Danielle DeLucy

$229

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Jun 21, 2018

FDA Compliant QC and QA Practices: to Create a Perfect Audit –Ready QMS

Joy McElroy

$249

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Jun 12, 2018

Human Factors and Usability Studies following ISO 62366 and the new FDA Guidance

Edwin Waldbusser

$249

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May 23, 2018

OSHA Law Update 2018: Conducting OSHA 300 Log Record-keeping Training

Joe Keenan

$229

Order now

May 22, 2018

2018 Update -FDA's Two New Draft Guidance on Software and Device Changes and the 510(k)

Carolyn Troiano

$249

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May 03, 2018

2018: FDA's New Inspection Policy and Strategic Regulatory Updates

Carolyn Troiano

$249

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Apr 18, 2018

Sterility Failure Investigations – A Step-by-Step Process for Success

Danielle DeLucy

$249

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Apr 17, 2018

Steam Sterilization Microbiology and Autoclave Performance Qualification

Danielle DeLucy

$229

Order now

Mar 19, 2018

FDA Issues Final Guidance on "Deciding When to Submit a 510(k) for a Change to an Existing Medical Device"

Angela Bazigos

$359

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Mar 13, 2018

2018 Update: How to Write an Effective SOPs for FDA inspection & Regulatory Compliance

Angela Bazigos

$249

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Feb 22, 2018

New FDA Guidance- Medical Device Human Factors Validation Testing Following ISO 62366

Edwin Waldbusser

$249

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Feb 08, 2018

21CFR Part11 Conformance for Medical Devices

Edwin Waldbusser

$249

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Jan 23, 2018

Annual Product Reviews : New FDA Quality Metrics Guidance on Annual Product Review

Danielle DeLucy

$249

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Jan 18, 2018

Conducting a Software Validation of Medical Device to Meet FDA Requirements

Edwin Waldbusser

$249

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Jan 09, 2018

Project Management for Computer Systems Validation and 21 CFR 11 / Annex 11

Angela Bazigos

$249

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Dec 19, 2017

NEW ISO/IEC 17025:2017 Update-The New Standard For Laboratory Competence

Michael Brodsky

$249

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Dec 12, 2017

Total Organic Carbon Analysis for Cleaning Validation in Pharmaceutical Manufacturing

Joy McElroy

$259

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Nov 20, 2017

FDA Software Validation and Verification, Computer System Validation: Step-by-Step

Carolyn Troiano

$249

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Nov 03, 2017

FDA Announces Final Guidance on Drug Pharmacy Compounding

Rachelle D'Souza

$249

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Oct 31, 2017

FDA Regulations -2017 on GMP Environmental Monitoring -Maintaining a Clean Room

Roger Cowan

$229

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Oct 26, 2017

Regulatory Considerations for Environmental Monitoring Investigations

Carl Patterson

$249

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Oct 09, 2017

How to go Paperless in an FDA-Regulated Environment using Electronic Workflow Signature Approvals and Electronic Records

Carolyn Troiano

$249

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Sep 18, 2017

Update 2017 on Patient's Medical Record :Disposition of Records and Records Retention, Including Electronic Records

Mark Brengelman

$249

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Sep 14, 2017

Deviation Investigation Best Practices: Ensuring Correct Content and Conclusions

Danielle DeLucy

$229

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Sep 13, 2017

Medical Device Cyber-Security Following New FDA Guidance

Edwin Waldbusser

$229

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Sep 06, 2017

U.S. Import of FDA Regulated Products: Understanding the Entry Process

Dr. Rossano V. Gerald

$249

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Sep 06, 2017

Implementing a Change Control Quality System Successfully

Danielle DeLucy

$229

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Sep 05, 2017

Electronic Records and Signatures - 21 CFR Part 11: Basic Concepts

Edwin Waldbusser

$229

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Aug 25, 2017

FDA Regulation 2017- 3D Printing and Medical Devices

Rachelle D'Souza

$219

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Aug 16, 2017

Implementation and Management of GMP Data Integrity

Danielle DeLucy

$249

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Jul 28, 2017

Use of Electronic Health Record Data (EHR) in FDA regulated clinical investigations

Rachelle D'Souza

$249

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Jul 26, 2017

Conducting a Successful Supplier Audit

Danielle DeLucy

$249

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Jul 20, 2017

Sterile Filtration of Pharmaceutical Products - Validation and Regulatory Requirements

Roger Cowan

$249

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Jul 14, 2017

GMP Environmental Monitoring for Pharmaceutical Clean Rooms

Roger Cowan

$229

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Jul 06, 2017

Best Practices in Lean Complaint Management in Compliance with FDA and ISO Regulations

Jeff Kasoff

$249

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Jun 23, 2017

Understanding Aseptic Technique and Clean room Behaviour

Danielle DeLucy

$249

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Best Quality Trainings in Lowest Price

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