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Online Events on Operations (past events)
Online Events on Operations
(past events)
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Production Conferences
Manufacturing Conferences
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Capa Conferences
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Showing 245 conferences
Business Process Management (BPM) Training
Oct 2024
Operational Risk Management MasterClass - EU
Oct 2024
Microbiological Contamination Control MasterClass - US
Jul 2024
Implementation of a Successful Technology Transfer Process
Nov 2023
Statistical Analysis for Process and Product Development
May 2023
Business Transformation & Operational Excellence APAC
Apr 2023
Refining Blending
Mar 2023
HPAPI Handling & Manufacturing Summit
Sep 2022
Behavioural Good Manufacturing Practices MasterClass
Sep 2022
International Conference on Clean and Sustainable Production (ICCSP)
Aug 2022
International Conference on Energy Production and Management
May 2022
EcomWorld Conference
May 2022
HR Forum
Mar 2022
No-Code Day: Manufacturing Industry
Mar 2022
Nuclear New Builds
Mar 2022
Connected Worker & OpEx
Feb 2022
GPS Spoofing Techniques and Procedures
Jan 2022
CXN Live: Future CX & Contact Center Trends & Technology APAC
Nov 2021
SAP Digital Supply Chain Live
Sep 2021
OPEX and Business Transformation
Sep 2021
Smart Manufacturing Summit
Sep 2021
Future Pharma
Aug 2021
Canadian Crude Logistics Conference
Jul 2021
Global Mobility and Remote Assignments MasterClass
Jul 2021
Blockchain for Business Summit
Jun 2021
Biologics Formulation Development and Drug Delivery Forum
Jun 2021
Risk Americas Convention
May 2021
The Internal Communications Conference Amsterdam
Apr 2021
Health, Safety & the Environment: How Can You Lead the Way During and After the Crisis
Mar 2021
Pharma Contract Manufacturing Exchange
Mar 2021
Advanced S&OP and Integrated Business Planning Excellence
Mar 2021
APRICOT - Asia Pacific Regional Internet Conference on Operational Technologies
Mar 2021
Decommissioning Of Offshore Oil And Gas Installations
Aug 2020
Global Entrepreneurship Summit
Jul 2020
Managing Supply Chain Disruptions
Jul 2020
ACH Government Payment Processing - Handling Death Notification Entries (DNEs) and Reclamations
Jun 2020
Predictive Profiling
May 2020
Service Level Agreements Masterclass
Apr 2020
Human Factors Engineering to Satisfy the New IEC 62366-1, -2
Aug 2019
IQ, OQ, PQ in the Verification and Validation Process
Aug 2019
Statistical Justification for Sample Size and the Use of Only 3 Lots for Process Validation
Aug 2019
Adjustable Rate Mortgage (ARM) Rule
Aug 2019
4-Hour Virtual Seminar on Batch Record Review and Product Release
Jul 2019
Big Data in FDA-Regulated Industry - Best Practices for Systematic Use
Jul 2019
Effective Records Management and Document Control for Medical Devices
Jul 2019
Statistical Process Control - Keys to Prevent Process Variation and Ensure Quality
Jul 2019
I-9 Audits: Strengthening Your Immigration Compliance Strategies
Jul 2019
Monitoring High Risk Transactions
Jun 2019
Using Kanban JIT Systems to Run a Startup Plant
Jun 2019
Master Validation Plan - The Unwritten Requirements
Jun 2019
What is the harm in that? Risk Management 101
Jun 2019
Implementing Operational Risk in Foreign Exchange Activities
Jun 2019
FDA`s 21 CFR Part 11 Add-on Inspections
Jun 2019
Zero-Injury Workplace Culture vs. Safety Culture
Jun 2019
Good Laboratory Practices (GLPs) vs GMPs - Comparisons and Contrasts
Jun 2019
FDA`s Risk Evaluation and Mitigation Strategy (REMS)
May 2019
Storm Water Pollution Prevention Plans (SWPPP)
May 2019
The Essentials of Managing Operational Risk
May 2019
Establishing and Regaining Control of Cleanroom
May 2019
The Business Case for LGBT Inclusion in the Workplace: Navigating Policies, Procedures, Practices and Bathrooms
May 2019
Integrating Cyber Risks in the ERM Plan
May 2019
Good Manufacturing Practices – 3 Hour Virtual Seminar
May 2019
The Dos and Don’ts of Poster Compliance - Is Your Company in Compliance with the Poster Requirements?
May 2019
Supplier Qualification - Important Part of Quality Systems and Supply Chain Management
May 2019
Root Cause Analysis and CAPA using 8-D Problem Solving Method
May 2019
USA Import Compliance Program and Written Procedures
Apr 2019
Human Error Investigations, Root Cause Determination and CAPA Effectiveness
Apr 2019
Contemporary Case Management Staffing and Models: Best Practices in the Era of Value-Based Purchasing
Apr 2019
Technical Report Writing
Apr 2019
Effective Cleaning Validation Procedures – Best Practices
Apr 2019
Risk Based Monitoring for GCP Compliance
Mar 2019
EO Sterilization Validation / Revalidation per ISO 11135
Mar 2019
Human Error Reduction in GMP Related Environments
Mar 2019
Integrating Lean and Project Management
Mar 2019
Preparing for a BSA/OFAC Regulatory Examination
Mar 2019
How to Write Effective 483 and Warning Letter Responses
Mar 2019
Best Practice Case Management Roles and Functions: How to Optimize RN and Social Worker Skill Sets
Mar 2019
How to Write Effective 483 and Warning Letter Responses
Mar 2019
Additive / 3D Printing Manufacturing and Its Regulatory Issues
Mar 2019
ISO 13485: 2016 Requirements and Compliance to Latest Updates
Feb 2019
SR Letter 11-7 – Supervisory Guidance on Model Risk Management
Feb 2019
Human Error and Cognitive Load: How to Reduce Memory and Attention Failures
Feb 2019
Lock Out Tag Out - Zero Energy Assurance : How to Prevent Common Accidents and Amputations and avoid OSHA penalties for non-compliance - Repair, Service, Set Up of Machinery
Feb 2019
Successful Water System Sanitization
Feb 2019
Process Capability for Normal and Non-Normal Data
Feb 2019
SR Letter 11-7 - Supervisory Guidance on Model Risk Management
Feb 2019
Complaint Handling, MDR`s & Recalls
Feb 2019
ASTM 2500: Lessons Learned Through a Decade of Implementation
Feb 2019
How to Develop, Implement and Manage an Effective Change Control Program
Jan 2019
Confirming your Compliance to ISO 13485:2016 Requirements
Jan 2019
Technical Writing for the Regulated Industries
Jan 2019
FDA Regulations for Analytical Instrument Qualification and Validation – Comprehensive Best Practices
Dec 2018
Complaint Handling Requirements – Interrelationship with CAPA, Change Control, Adverse Event Reporting and Recalls, Life Cycle Process Activities
Dec 2018
How to Perform a Thorough Root Cause Analysis and CAPA Development
Dec 2018
Human Error Prevention in Pharmaceutical Manufacturing
Nov 2018
Conducting Successful Quality Audits
Nov 2018
Root Cause Analysis and Corrective Action
Nov 2018
Becoming a Chief Audit Executive - Leading the Internal Audit Function
Nov 2018
Auditing and examining Travel and Entertainment Expenses: Expense Reimbursement Fraud
Oct 2018
Workplace Violence Prevention Programs Including Active Shooter Scenarios
Oct 2018
FDA’s Adverse Event Reporting and Product Recalls
Oct 2018
Introduction to Design of Experiments
Oct 2018
Microsoft Excel: Using What-If Analysis-When, Why, and How
Oct 2018
Change Control Procedures in Regulated Industries
Oct 2018
Aseptic Process Overview and Validation
Oct 2018
Recent FDA Auditing Practices and the Top 10 Most Common Cited GMP Deficiencies
Sep 2018
Tougher Supplier Controls – Avoid Unwanted Changes
Sep 2018
Controlling Human Error in the Manufacturing Floor
Sep 2018
Process Validation LifeCycle
Sep 2018
Chipping away at constraints – Practical tips to Improve your Manufacturing Operations
Sep 2018
CGMP controlled Raw Materials
Sep 2018
Laboratory Controls – Anticipate the Systems Based FDA Inspection
Sep 2018
Vendor Selection and Management
Sep 2018
Marketing to Medicare or Medicaid Beneficiaries - What You Can and Cannot Do
Aug 2018
Tools for Human Error Reduction
Aug 2018
Effective Project Audit Implementation: Quality, Cost, Procurement Management
Aug 2018
Process Validation – Principles and Protocols
Aug 2018
Agile HR 101: Applying Agile to Human Resources
Aug 2018
HACCP – Hazard Analysis and Critical Control Points
Aug 2018
Microsoft Excel - Let`s Look Beyond the Look-Up
Aug 2018
The Psychology and Law of Harassment Investigations
Aug 2018
CMS Hospital CoP and TJC Telemedicine Standards, Telemedicine Credentialing and Privileging
Jul 2018
Get Lean, NOT Mean – Secrets of the Toyota Production System
Jul 2018
Through the Eyes of an Auditor
Jul 2018
Payment Risk Management and Fraud Control
Jul 2018
Developing a Contractor Safety Program
Jul 2018
Beyond Annual Performance Reviews: How to develop Employee Performance Year-around
Jul 2018
Onboarding In A GMP Environment – Best Practices
Jul 2018
BSA Training - Tips & Tools
Jul 2018
Practical Risk Appetite and Risk Tolerance
Jul 2018
The Low-down on ACH and Regulation E
Jun 2018
Validation of GC/ GC-MS Methodologies
Jun 2018
Introduction to Good Manufacturing Practices (GMP)
Jun 2018
Form W-2 for : All You Need to Know
May 2018
The Audit Role and Strategies for Business Continuity Planning (BCP)
May 2018
Acceptance Activities in FDA QSR
Feb 2018
Understanding, Calculating, and Using Statistical Power
Nov 2017
Process Reliability Modeling: Driving Organizational Success
Aug 2017
Effective Supplier Qualification Program
Aug 2017
Risk-Based Audit Methodology: How to Achieve Enterprise Security
Jul 2017
Writing Effective Standard Operating Procedures and Work Instructions
Jun 2017
Proper Execution of Annual Product Reviews
Jun 2017
Overhauling Outdated Credit Decisioning: Understanding and Best Practices
May 2017
How to Prepare for a Customs Focused Assessment Audit and Self Audit your Import Program
May 2017
Good Deviation Practice: What you need to know
May 2017
Theory of Constraints
Apr 2017
ISO 13485:2016 Utilizing Lean Documents and Lean Configuration
Apr 2017
Understanding Corrections and CA&PA
Apr 2017
Design Inputs Design Outputs Traceability Matrix
Apr 2017
Acceptance Sampling by Variables
Apr 2017
Preparation for GMP Inspections by Regulatory Agencies
Apr 2017
Understanding Proper Application of Risk Assessment
Mar 2017
10 Keys for Maximizing the Benefits of your SPC Program
Feb 2017
Conducting Successful Product Complaint Investigations
Feb 2017
CAPA Training and Causes of Warning Letters due to Lack of Comprehension
Feb 2017
When Regulation E and ACH Don`t Align
Dec 2016
Improving Data Governance in Higher Education
Dec 2016
Construction of the European Drug Master File (EDMF) for Regulatory Agencies - Webinar by GlobalCompliancepanel
Dec 2016
Good Laboratory Practices (GLPs) - Comparing and Contrasting with Good Manufacturing Practices (GMPs)
Nov 2016
Establishing a Revenue-Generating Corporate Engagement Program
Oct 2016
Using Lean to Streamline your Continuity Planning and Recovery
Oct 2016
Quality Metrics Program: FDA Challenges and Requirements including the New `Quality Metrics Technical Conformation Guide` Released
Sep 2016
Improving Internal Customer Outcomes in Shared Services
Sep 2016
Understanding Vendor Verification and Monitoring Programs for Food Manufacturing
Sep 2016
What Sample Size Do I Need?
Sep 2016
The Value of Analytics for Achieving Successful Manufacturing Process Transfer
Aug 2016
Service Level Agreements (SLAs) - Preparation Guidelines for Effective SLAs
Aug 2016
Controlling Food Safety Risks: Implementation and Audit in Accordance with FSSC 22000
Jul 2016
Using Analysis of Variance (ANOVA) - A Practical Approach
Jul 2016
Proper CAPA Management and Root Cause Analysis
Jul 2016
Developing an Effective HR Audit and Compliance Committee
Jul 2016
Tools for Human Error Reduction: Developing Metrics and KPI`s (Key Performance Indicators) to minimize Human error rates
Jun 2016
Shared Services: Assessing Your Readiness
Jun 2016
Getting Ready for Proposed FFIEC Call Report Changes
Jun 2016
Achieving Compliance with Robust CAPA Systems
Jun 2016
Financial Statement Audit Best Practices
May 2016
Acceptance Sampling by Variables
Apr 2016
Optimizing Target Weights for Foods and Beverages
Mar 2016
Sampling Plans for Process Validation and Production Lot Acceptance
Feb 2016
Controlling Human Error in the Manufacturing Floor
Jan 2016
Regulation V - Fair Credit Reporting Act
Jan 2016
Executing Strategy: Synergizing Your People, Operations and Processes With Results
Jan 2016
Writing Effective Policies and Procedures
Dec 2015
Analytics-based Enterprise Performance Management for Optimal Decisions
Nov 2015
Supply Chain Profitability - Achieve Competivitive Edge by Reducing Costs & Improving Performance
Oct 2015
Introduction to Risk Assessment
Sep 2015
Applying Statistical Process Control Effectively
Aug 2015
Meeting Annual U.S. FDA cGMP Training Requirements
Aug 2015
ISO/FDIS 9001: - Planning for the Changes
Aug 2015
The Middlesex MBA by distance learning
Aug 2015
Structuring Successful Outsourcing Contracts for Campus Services
Aug 2015
Student Affairs Fundraising: Building a Sustainable Structure
Aug 2015
21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Configuration
Jul 2015
A Risk-Based Methodology to Develop and Prepare an Effective Service Level Agreement (SLA) Package to Improve Service and Security Quality
Jul 2015
Preparing Your Institution for Shared Services Implementation
Apr 2015
Traceability Matrix - Principles of Lean Documents and Lean Configuration
Apr 2015
Process Validation - Statistical Process Control
Mar 2015
Airport Traffic Control Tower (ATCT)
Feb 2015
A Strategic Approach to Operational Budgeting
Jan 2015
Marine Salvage Law
Jan 2015
Pharmaceutical and Chemical Classification under the Harmonized Tariff Schedule
Jan 2015
The Value of Hourly Cost Maintenance Programs
Oct 2014
SOP and FDA Compliance
Aug 2014
Assessing Your Institution`s Readiness for Shared Services
May 2014
Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration
Mar 2014
Medical Devices and Pharmaceutical Quality Management System - Applying the Principles of Lean Documents and Lean C
Jan 2014
Best Techniques for Hiring and Retaining Global Talent
Nov 2013
How to Manage a Medical Device Recall Efficiently and Effectively
Jul 2013
Construct and Manage the Technical File and Design Dossier
Jul 2013
Offensive Behavior Investigation
Jun 2013
Effective OSHA Auditing - Creating Audit Documents for a Successful OSHA Audit
Mar 2013
The World of Enterprise Mobility
Mar 2013
New Finalized HITECH Amendments to HIPAA - How Policies and Practices Must Be Changed
Jan 2013
Acceptance Sampling by Variables Using Z1.9
Jun 2012
Modeling and Optimizing Process Behavior using Design of Experiments
Apr 2012
Predicting Warranty Expense Using Reliability Analysis Methods
Mar 2012
Transatlantic Shared Services and Outsourcing Week Online
Feb 2012
Setting up an effective Internal Audit Program
Feb 2012
Record Keeping for a (Food) Recall: Keeping Records to Minimize the Affect of a Recall
Jan 2012
How to Audit remotely using Online Auditing Techniques
Jan 2012
GMP Annual Training
Dec 2011
Lyophilization Process Development and Cycle Design
Nov 2011
Master Production Record Requirements - Webinar By GlobalCompliancePanel
Jun 2011
Webinar on Specification Development - Webinar By GlobalCompliancePanel
Jun 2011
How to successfully create a Device History Record and keep FDA happy in the process - Webinar By GlobalCompliancePanel
Apr 2011
An Advanced course on Lean Documents and Document Control
Apr 2011
Social Media in a Regulated Environment - ComplianceOnline Banking and Financial Training
Mar 2011
ISO 13485 as a Quality Management System for Medical Devices - Webinar By GlobalCompliancePanel
Dec 2010
The FDA`s Working Group Reports, I & II - New Directions - Webinar By GlobalCompliancePanel
Dec 2010
Introduction to Operational Risk - Webinar by GlobalCompliancePanel
Dec 2010
The Riskability Exercise – creating a EGRCM culture and technology deployment - ComplianceOnline Risk Management Webinar
Nov 2010
Good Documentation Practices in a Regulated Environment - Webinar by GlobalCompliancePanel
Nov 2010
The Tougher U.S. FDA - One Year Later
Oct 2010
ComplianceOnline Webinar - Estimating Greenhouse Gas Emissions; Determining Your Carbon Footprint
Oct 2010
Active and Intelligent Packaging Technologies: A Food Safety and Quality Perspective
Oct 2010
Critical Role of Quality Audit in GxP Compliance & Improvement
Sep 2010
Effective Quality Process Improvement for Medical Device Firms: Don’t get caught managing process through standardized SOP’s
Sep 2010
Compiling the Design History File, and Technical File / Design Dossier - Webinar by GlobalCompliancePanel
Sep 2010
Medical Devices in the EU: CE Mark and 93/42/EEC Directive
Sep 2010
Developing an ethylene oxide (EO) sterilization process for a product with limitations
Sep 2010
Understanding Acceptance Activities for Medical Devices - Webinar by GlobalCompliancePanel
Sep 2010
Key Modules of an Effective CAPA SOP - Webinar by GlobalCompliancePanel
Sep 2010
Good Documentation Practices for GMP Operations - Webinar by GlobalCompliancePanel
Sep 2010
Product Risk Management - ISO 14971 and ICH Q9
Aug 2010
Importing and Exporting Medical Devices: A Primer on Regulatory Strategy and Requirements - Webinar by GlobalCompliancepanel
Aug 2010
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