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Home ›  Laboratory Compliance

Laboratory Compliance Regulations Training, Compliance Best Practices and Standards

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Webinar
Total Organic Carbon Analysis for Cleaning Validation in Pharmaceutical Manufacturing
17
/ Apr
Thursday-2025

Total Organic Carbon Analysis for Cleaning Validation in Pharmaceutical Manufacturing

  • Speaker: Joy McElroy
  • Product ID: 705929
  • Duration: 90 mins
In this cleaning validation webinar attendees will learn the Total Organic Carbon (TOC) feasibility, method validation and transfer from the laboratory to the manufacturing floor, as well as reviewing a feasibility study of multiple, difficult to oxidise or low solubility organic compounds.
* Per Attendee
$199
View Details
Webinar
Ethylene Oxide (EO) Sterilization Basics for R&D Engineers
17
/ Apr
Thursday-2025

Ethylene Oxide (EO) Sterilization Basics for R&D Engineers

  • Speaker: Gerry O Dell
  • Product ID: 701272
  • Duration: 90 mins
This Sterilization training will provide valuable information to companies that design products for terminal sterilization with ethylene oxide.
* Per Attendee
$199
View Details
Webinar
Performing Effective Management Review of the Quality System
19
/ May
Monday-2025

Performing Effective Management Review of the Quality System

  • Speaker: David L Chesney
  • Product ID: 704933
  • Duration: 90 Min
This webinar will teach you how to conduct an effective management review of the quality system which helps you understand how to plan and focus on right metrics and governed by an efficient process. Participants will also understand FDA policy regarding disclosure of management review information during inspections.
* Per Attendee
$199
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Seminar
Quality Control Laboratory Compliance - cGMPs and GLPs

Quality Control Laboratory Compliance - cGMPs and GLPs

Simu Live
On-demand Streaming - Virtual Training Through WebEx

Kelly Thomas

Vice President, Americas Quality Operations at Stallergenes Greer
* For one Registration

$1199

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Seminar
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)

Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)

Simu Live
On-demand Streaming - Virtual Training Through WebEx

Mark Powell

Director, Mark Powell Scientific Limited
* For one Registration

$1199

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Seminar
Sustainable Compliance for Out of Specifications (OOS) Results, Deviations, and Corrective and Preventive Actions (CAPA)

Sustainable Compliance for Out of Specifications (OOS) Results, Deviations, and Corrective and Preventive Actions (CAPA)

Simu Live
On-demand Streaming - Virtual Training Through WebEx

Rajesh K Gupta

Visionary Scientific and Compliance Consultant, Biologics Quality & Regulatory Consultants, LLC
* For one Registration

$1199

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Seminar
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)

Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)

Simu Live
On-demand Streaming - Virtual Training Through WebEx

Mark Powell

Director, Mark Powell Scientific Limited
* For one Registration

$1199

View Details
Seminar
Laboratory Inspection and Auditing

Laboratory Inspection and Auditing

Simu Live
On-demand Streaming - Virtual Training Through WebEx

Mark Powell

Director, Mark Powell Scientific Limited
* For one Registration

$649

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Seminar
Conducting Effective Investigation of Out-of-Specs and Atypical Laboratory Data

Conducting Effective Investigation of Out-of-Specs and Atypical Laboratory Data

Currently This Seminar is in the process of Getting Scheduled
Wanted to have it scheduled near your city
Pre-Register (no payment required) yourself and get the official Invite Once dates are announced for this seminar.
Call +1-888-717-2436 or email at customercare@complianceonline.com with your Name, Email and Preferred Month and Location for this seminar
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Recorded/CD
GMP Compliance for Quality Control and Contract Laboratories

GMP Compliance for Quality Control and Contract Laboratories

  • Speaker: David L Chesney
  • Product ID: 706869
  • Duration: 90 Min
This webinar will cover the requirements for laboratory controls under US GMP regulations, such as those relating to equipment calibration and preventive maintenance; sample chain of custody; good documentation practices; investigation of out of specification and out of trend results; analytical method validation; change control; impact of staffing levels and work flow patterns in the lab on GMP compliance; training and other issues.
CD/Recorded
$249
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Recorded/CD
Good Laboratory Practices by Using The Quality Management System (QMS)

Good Laboratory Practices by Using The Quality Management System (QMS)

  • Speaker: John Fetzer
  • Product ID: 706858
  • Duration: 4 Hrs
This GLP quality system webinar provides a general overview of the Proposed Rule, a GLP QMS and its implementation, GAP analysis, Plan-Do-Check-Act cycle, process control and optimization theory and quality audits are utilized for the analysis of an existing QMS and the potential benefits, barriers steps to implementing an optimized GLP QMS.
CD/Recorded
$399
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Recorded/CD
FDA Ambitious Regulation of Social Media and Corporate Responsibility

FDA Ambitious Regulation of Social Media and Corporate Responsibility

  • Speaker: Casper Uldriks
  • Product ID: 703853
  • Duration: 60 Min
FDA regulates advertising and promotion material as labeling. The legal definition of labeling covers just about anything that explicitly or implicitly conveys a message intended to affect a person’s behavior and decision outcomes. How FDA applies its legal tenants of false and misleading information or variations on that theme requires continual updating by FDA and constant re-evaluation by industry. Now the regulatory landscape involves other federal agencies and academic principles in psychology. It has become very complicated and will prove very costly if you knowingly or unknowing walk into one of FDA’s legal snares. This webinar will bring attendees up to speed so you are clearer about what is a problem, what is not a problem and what becomes a risk laden judgment call.
CD/Recorded
$219
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Recorded/CD
How to Prepare a Standard Operating Procedure (SOP)?

How to Prepare a Standard Operating Procedure (SOP)?

  • Speaker: Dr. Afsaneh Motamed Khorasani
  • Product ID: 705131
  • Duration: 60 Min
This webinar will detail a step-by-step procedure on how to write a practical, effective and compliant Standard Operating Procedures (SOPs), review and revise SOPs and maintain compliance over the course of the SOP life-time.
CD/Recorded
$199
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Standard
Document Controls Group(all SOP's listed below)

Document Controls Group(all SOP's listed below)

  • Provider: Med_Device_Advisors
$200
View Details
Standard
Laboratory Notebook Control

Laboratory Notebook Control

  • Provider: Med_Device_Advisors
$100
View Details
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