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Online Events on Innovations (past events)
Online Events on Innovations
(past events)
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Showing 278 conferences
UIN Conference on Economics and Business (UINACEB)
Nov 2024
International Commercial Contracts School Training Course
Sep 2024
Modernize Clinical Technology
Aug 2024
International Conference on Advanced Nanoscience and Technology (ANaNO)
Apr 2024
Sales Development Excellence
Oct 2023
International Competitive & Market Intelligence Conference
Jun 2023
Technology Matters Marathon
May 2023
Responsible Business Asia
May 2023
Statistical Analysis for Process and Product Development
May 2023
Eurasia Gulf Online Startup Forum
Dec 2022
AI in Clinical R&D Summit
Nov 2022
TECH ARENA UK
Nov 2022
Sustainability in Creative Industries
Nov 2022
Knowledge Management Reborn Modern KM: Latest Technologies & Strategies
Sep 2022
Spikes Asia Academy : THE NEXT
Sep 2022
International Conference on Innovative Practices in Technology and Management
Jun 2022
Auto Tech
Jun 2022
Innovative Glazing Global Summit
Apr 2022
Innovative Curing & Tire Building Forum
Mar 2022
DX3 CANADA
Mar 2022
Avoiding Pitfalls in Patent/Know-How Licences and R&D Collaborations
Mar 2022
UK Smart Cities Mission to Malaysia
Feb 2022
Innovation Arabia Annual Congress
Feb 2022
Connected Worker & OpEx
Feb 2022
Quality Control Laboratory Compliance - cGMPs and GLPs
Feb 2022
NFT Confex
Feb 2022
Carbon Neutral Vehicles & LCA Congress
Jan 2022
MoneyNext Summit
Nov 2021
Technology & Innovation North America
Nov 2021
Asian Forum on Enterprise for Society
Sep 2021
R&D Product Development & Design Thinking Summit
Sep 2021
Strategic Resource & Portfolio Management
May 2021
Chief Innovation Officer Summit
May 2021
FITC Toronto - The Technology & Creativity Conference
Apr 2021
Design Thinking Virtual (#DTVX)
Apr 2021
Medical Writing for Medical Devices
Mar 2021
Innovative All-Season & Winter Tire Development Forum
Mar 2021
Patentability and State of the Art Searching
Feb 2021
Writing Effective SOPs for QMS
Dec 2020
Pharmacovigilance
Dec 2020
World Innovators Meet
Dec 2020
Consumer-Focused R&D | R&D Performance Management
Nov 2020
Product Launch Excellence for Pharma & Biotech
Nov 2020
Business Development and Licensing in Pharma and Biotech
Nov 2020
Circular, Zero Waste Textiles
Nov 2020
International Food, Nutrition and Bioprocess Technology Conference (Food & Nutrition)
Oct 2020
Manufacturing Leaders` Summit EMEA
Oct 2020
WIRED Smarter
Oct 2020
International Conference on Neuroscience and Neurochemistry
Sep 2020
European Congress on Vaccines R&D & Vaccination
Aug 2020
International Conference on Design Engineering and Product Innovation (ICDEPI)
Jul 2020
Normality Tests and Normality Transformations: Explanations, Justifications, and Uses
Jun 2020
Statistical Analysis of Gages (Metrology)
Feb 2020
Bad Standard Operating Procedures (SOPs) - Bad Training: Garbage In, Garbage Out
Aug 2019
IQ, OQ, PQ in the Verification and Validation Process
Aug 2019
Design of Experiments for Non-Statisticians
Aug 2019
Statistical Justification for Sample Size and the Use of Only 3 Lots for Process Validation
Aug 2019
Prescription and Over-the-Counter GMPs: Avoiding FDA Form 483 and Making the Best Decisions
Aug 2019
Big Data in FDA-Regulated Industry - Best Practices for Systematic Use
Jul 2019
6-Hour Virtual Seminar on Adaptive Design for Clinical Trials
Jul 2019
4-Hour Virtual Seminar on Aseptic Processing and Validation
Jul 2019
Effective Records Management and Document Control for Medical Devices
Jul 2019
Writing Validation Master Plans - Best Practices for Writing a Compliant Document
Jul 2019
Root Cause Analysis - Starting at the Beginning
Jul 2019
Better Alternatives to AQL Sampling Plans for Risk Management in Incoming QC
Jun 2019
Top Process Validation Mistakes - And How to Avoid Them
Jun 2019
FDA Quality System Inspection Technique (QSIT) Audits – Good Preparation Practices
Jun 2019
Master Validation Plan - The Unwritten Requirements
Jun 2019
Solving Statistical Mysteries – What does the FDA want
Jun 2019
FDA`s 21 CFR Part 11 Add-on Inspections
Jun 2019
Good Laboratory Practices (GLPs) vs GMPs - Comparisons and Contrasts
Jun 2019
Best Practices to Obtain FDA Feedback Prior to 510(k) and De Novo
Jun 2019
Lyophilization Process Development and Cycle Design with a Case Study
Jun 2019
How to Prepare a Standard Operating Procedure (SOP)?
May 2019
CDISC Mapping 4: SDTMs and ADAMs Examples (80%/20% Mapping Rule)
May 2019
New Elemental Impurities Tests for Pharmaceutical Products According to the New ICH Q3D and USP 232/233 Guidelines
May 2019
Root Cause Failure Analysis Closed Loop Corrective Action
May 2019
Storm Water Pollution Prevention Plans (SWPPP)
May 2019
Ethylene Oxide (EO) Sterilization Basics for R&D Engineers
May 2019
Implementing a Metrics Program - Uncovering and Overcoming the Challenges
May 2019
Data Quality Culture and Building a Corporate Data Integrity Plan
May 2019
Quality by Design (QbD) in Pharmaceutical and Medical Device Manufacturing
May 2019
Good Manufacturing Practices – 3 Hour Virtual Seminar
May 2019
Statistical Hypothesis Tests: Concepts and Applications
May 2019
Design History Files and Technical Files/Design Dossiers - Meeting U.S. FDA CGMPS and the EU`s MDD Requirements
May 2019
Supplier Qualification - Important Part of Quality Systems and Supply Chain Management
May 2019
Stability Studies & Estimating Shelf Life
May 2019
Root Cause Analysis and CAPA using 8-D Problem Solving Method
May 2019
3-Hour Virtual Seminar on SOP Writing, Training and Compliance in the Pharmaceutical Industry
May 2019
Continued Process Verification - A Systematic Approach
Apr 2019
Estimating Reliability Performance with Accelerated Life Tests
Apr 2019
ANDA Submission and GDUFA Final FDA Guidance
Apr 2019
Complaint Management: Best Practices to Assure Compliance and Customer Retention
Apr 2019
Technical Report Writing
Apr 2019
Mastering Excel Formulas and Functions
Apr 2019
Understanding and Implementing a Technology Transfer Process
Apr 2019
Sampling – How Large a Sample Do I Need? Determining the Right Size for Accurate, Cost Effective Results
Mar 2019
EO Sterilization Validation / Revalidation per ISO 11135
Mar 2019
Process Capability Analysis using Confidence or Reliability Calculations
Mar 2019
Regulatory and Testing Requirements of the Bacterial Endotoxin Testing (BET) or LAL Program
Mar 2019
Managing Product and Process Risk through Failure Mode and Effects Analysis (FMEA)
Mar 2019
EU and US GMP/GDP – Similarities and Differences
Mar 2019
Device Changes, FDA Changes, and the 510(k)
Mar 2019
Quality System Regulations for Combination Products
Mar 2019
510(k) Update - How to Format Succinct and Comprehensive 510(k)s
Mar 2019
Additive / 3D Printing Manufacturing and Its Regulatory Issues
Mar 2019
ISO 13485: 2016 Requirements and Compliance to Latest Updates
Feb 2019
Medical Device Software 62304 Compliance
Feb 2019
Statistical Power – Understanding, Calculating, and How to Effectively Use it
Feb 2019
Design Verification, Validation and Testing for Medical Devices
Feb 2019
USP [1224] Transferring the Method to meet Regulatory Expectations
Feb 2019
How to Conduct a Quality Management System Audit to ISO/IEC 17025:2017
Feb 2019
Understanding FDA Design Verification and Validation Requirements for Medical Devices
Feb 2019
Confidence/Reliability Calculations of Product and Product Capability
Feb 2019
What FDA-Regulated Industry Should Know about FDA’s New Policy on GMP Enforcement
Jan 2019
Statistical Process Control (SPC)
Jan 2019
QbD Development Process Evaluating Critical Steps
Jan 2019
Technical Writing for the Regulated Industries
Jan 2019
Confirming your Compliance to ISO 13485:2016 Requirements
Jan 2019
Translating Academic Assays for GLP Use
Jan 2019
Supply Chain and Product Compliance Using RoHS, REACH, and Conflict Minerals
Jan 2019
Human Factors Engineering in New Product Development
Jan 2019
Human Factors Engineering in New Product Development
Jan 2019
FDA and EMA Global Labeling Challenges and Requirements
Jan 2019
How to Use the FDA’s Final Guidance to Correctly Label Biosimilar Products
Jan 2019
Writing Effective Standard Operating Procedure (SOPs) and Work Instructions (WIs)
Jan 2019
Getting R&D on Board with Risk Analysis
Dec 2018
Selecting Right Statistical Tools to Solve Problems
Dec 2018
Developing IQ, OQ, PQ Protocols as Part of a Validation Plans
Dec 2018
FDA Regulations for Analytical Instrument Qualification and Validation – Comprehensive Best Practices
Dec 2018
Implementing a Risk-Based Internal cGMP Annual Audit Program
Dec 2018
How to Perform a Thorough Root Cause Analysis and CAPA Development
Dec 2018
Risk Management Techniques for Medical Devices
Nov 2018
Process Verification and Validation
Nov 2018
Ensuring Integrity and Security of Laboratory Data
Nov 2018
Meet the Tougher U.S. FDA CGMPs
Nov 2018
Human Error Prevention in Pharmaceutical Manufacturing
Nov 2018
Data Analysis in QSR - Techniques and Tools to avoid Warning Letter
Nov 2018
Effective Quality by Design (QbD)
Oct 2018
Computer System Validation
Oct 2018
Sterilization of Pharmaceutical Products and Medical Devices
Oct 2018
Troubleshooting Ethylene Oxide (EO) Processes
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
FDA’s New Guidance’s Deciding When to Submit a 510(k) for Device and Software Changes
Sep 2018
Process Validation LifeCycle
Sep 2018
Chipping away at constraints – Practical tips to Improve your Manufacturing Operations
Sep 2018
Supply Chain Issues (21 CFR Part 820.50 and 820.80) and Warning Letters
Aug 2018
Process Validation – Principles and Protocols
Aug 2018
HACCP – Hazard Analysis and Critical Control Points
Aug 2018
HPLC Instrument Qualification and Method Validation
Aug 2018
Design Control Basics
Aug 2018
FDA Compliant QC and QA Practices – Creating a Perfect, Audit-Ready QMS
Aug 2018
Laboratory Investigations for Out of Specification Results
Jul 2018
Good Documentation Guideline (Chapter <1029> USP)
Jul 2018
Forced Degradation Studies/ Biologics Stability Programs for Biopharmaceuticals
Jul 2018
Develop a Compliant Validation Protocol and Analytical Procedures according to the FDA Guidance and USP Good Documentation Practices
Jul 2018
Overview of Medical Device Regulation in Europe
Jun 2018
Approaching unknown cause laboratory investigations using lean tools
Jun 2018
Stability Programs for Leachable Impurities
Jun 2018
Differences Between ISO 13485 & ISO 9001 - and How to Choose Which One to Implement
Apr 2018
Discussion on Raw Material Methods and Specifications
Apr 2018
Equipment and Facility Qualification
Dec 2017
AAMI TIR 45: Agile Meets Software Standards, and we all Win
Nov 2017
Understanding, Calculating, and Using Statistical Power
Nov 2017
Medical Device Engineering Change Control
Oct 2017
GLP Quality System Essences and Comparison with GMP
Oct 2017
Data Integrity and Its Issues
Sep 2017
Effective Supplier Qualification Program
Aug 2017
How to Perform Measurement Systems Analysis
Jul 2017
Creating a Good Design History File (DHF) for Audit Success
Jul 2017
Identifying and Managing Emerging Operational Risks
Jun 2017
Writing Effective Standard Operating Procedures and Work Instructions
Jun 2017
Export Update: Compliance Challenges and Best Practices
Jun 2017
USA and Canada Food Marketing Claims
Jun 2017
Proactive Internal Auditing -The Key to Establishing, Maintaining, and Improving Quality Systems
Jun 2017
Dos & Don`ts Related to Information Security and Data Privacy
Jun 2017
Elements of a Corrective and Preventive Action (CAPA) Program and Uses of CAPA Data
May 2017
ISO 13485:2016 Utilizing Lean Documents and Lean Configuration
Apr 2017
Introduction to Design of Experiments
Apr 2017
Design Inputs Design Outputs Traceability Matrix
Apr 2017
Acceptance Sampling by Variables
Apr 2017
What You Should Know About Export Requirements for FDA Regulated Products from the US to Foreign Countries
Apr 2017
Preparation for GMP Inspections by Regulatory Agencies
Apr 2017
Balancing Customer Satisfaction With Security Issues
Mar 2017
Lyophilization Technology
Mar 2017
Data Analysis in QSR
Mar 2017
Classifying Medical Devices - US and EU
Mar 2017
Avoiding Critical R&D Formulation/Drug Delivery Errors
Mar 2017
Understanding Design Controls
Feb 2017
GMP Complaint Systems, Adverse Event Reporting and Product Recalls
Feb 2017
Techniques to engage information workers to improve Information Governance compliance
Feb 2017
Best Practices for Project Management of Clinical Trials
Feb 2017
The Marriage of the PFMEA and Control Plan
Jan 2017
Implementation of the Generic Drug Labeling Rules
Jan 2017
21 CFR Part 11 - Electronic Record and signature Validation
Dec 2016
Challenges of Change Control: Implementation and Maintenance
Nov 2016
Risks of Omission
Nov 2016
MEDDEV 2.7.1, Revision 4 for Clinical Evaluation and the Latest Guideline: A Guide for Manufacturers and Notified Bodies
Oct 2016
How to Use Big Data for AML/AB&C Compliance and Risk Mitigation
Oct 2016
Understanding Proper Labeling & Packaging Requirements & How to Stay Legally Compliant
Oct 2016
Regulation E - Basics and Error Resolution (ACH and Debit Card): Processing, Disclosure and Investigation
Sep 2016
Regulatory Document – Site Master File
Sep 2016
Good Documentation Practice for GxP Environments
Sep 2016
Medical Record Standards: What Hospitals Should Know About the CMS Hospital CoPs
Sep 2016
What Sample Size Do I Need?
Sep 2016
How to prepare for and Host FDA Inspection and Avoid 483`s
Sep 2016
Accelerated Aging Product Testing
Aug 2016
Clinical Trials be at Risk for Potential Fraudulent Billing. Conducting a Billing Risk Assessment and Coverage Analysis are Essential for Proper Billing.
Aug 2016
FSMA Gives FDA Recall Authority Over Adulterated Food and Broadens Standards for Food Detention
Aug 2016
Evolving Regulatory Expectations for Data Integrity in GMP laboratory
Aug 2016
What Sample Size Do I Need
Aug 2016
Good Manufacturing Practice for Nutraceuticals
Aug 2016
CAMELS Evaluation and Ratings System plus Examination of CCAR and CLAR
Jul 2016
TSCA Reform - What`s Next?
Jul 2016
Risk Assessment and Business Impact Analysis using PMI and ISO/IEC 21500 Project Management Methodologies
Jul 2016
Human Factors/Usability Based on ISO 62366
Jul 2016
USP <71> Sterility Testing: New Harmonization with International Compendia and Overview
Jul 2016
Tools for Human Error Reduction: Developing Metrics and KPI`s (Key Performance Indicators) to minimize Human error rates
Jun 2016
Understanding and Implementing the EU Vigilance System
Jun 2016
Compliance Failures - Detection, Prevention and Risk Mitigation Strategies
Jun 2016
Risk Management - Principles of Lean Documents and Lean Configuration
May 2016
Antimicrobial effectiveness test USP [51] : Overview and New Content Proposals
Mar 2016
Device Changes and the 510(k)
Mar 2016
Good Social Media Practices to Avoid FDA Actions
Jan 2016
Statistical Process Control
Jan 2016
The Controls for Outsourcing Manufacturing and Testing
Nov 2015
21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Configuration
Jul 2015
Best Practices for Quality Risk Management for the Pharmaceutical Industry
Jun 2015
Software Verification and Validation in Medical Industry
Jun 2015
Normality Tests and Normality Transformations
Jun 2015
South East Asia Regulatory Compliance for Life Science Products, Live Webinar
Jun 2015
Corrective and Preventive Action-Lean Management System
Jun 2015
Data Protection and Compliance under the EFPIA Disclosure Code
Apr 2015
Traceability Matrix - Principles of Lean Documents and Lean Configuration
Apr 2015
Process Validation - Statistical Process Control
Mar 2015
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
Robust Corrective And Preventive Action (CAPA)
Nov 2013
510(k) for IVDs
Nov 2013
Unique Device Identification (UDI) Final Rules Overview
Nov 2013
Construct and Manage the Technical File and Design Dossier
Jul 2013
Quality Practices for Research and Development (R&D) CMC Laboratories
Mar 2013
Immunogenicity to biologics: processes, impact on efficacy and safety, and management strategy
Feb 2013
Lean Project Management For U.S. FDA-Regulated Industries
Apr 2012
Modeling and Optimizing Process Behavior using Design of Experiments
Apr 2012
NLEA Regulation for Retail and Foodservice Labeling - Government Mandate and Additional Verbiage to Increase Food Safety and Brand Protection
Jan 2012
Medical Design & Manufacturing (MD&M Online)
Dec 2011
Lyophilization Process Development and Cycle Design
Nov 2011
Equipment Validation, Tracking, Calibration, and Preventive Maintenance - Webinar By GlobalCompliancePanel
Oct 2011
Proper Identification and Payment of Exempt Employees - Webinar By TrainHR
Sep 2011
Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities By compliance2go
Sep 2011
Effective Employee Performance Documentation: Elements and Techniques - Webinar By TrainHR
Jul 2011
ComplianceOnline Webinar - Why and How - Verification of Compendial Methods - USP [1226]
Apr 2011
Design Control Explained - Medical Device Webinar
Mar 2011
Don`t RISK to ignore RISKS. Understanding ISO 14971
Feb 2011
Design Validation Protocol and Acceptance Criteria for Chromatographic Methods to meet ICH requirements 2010
Jan 2011
Quality and Food safety - Problem Solving Methods (Steps, Tools & Success Key Factors) - ComplianceOnline Food Safety Webinar
Jan 2011
The FDA`s Working Group Reports, I & II - New Directions - Webinar By GlobalCompliancePanel
Dec 2010
QSR Device Inspections – Transition from “Barely Surviving” to “Gaining Control”
Nov 2010
Auditing API Manufacturers and Suppliers - Webinar by GlobalCompliancePanel
Nov 2010
Equipment Calibration, Maintenance, and Validation: What Auditors Look for in a Controlled Process
Nov 2010
Controlling Change to meet GMP Requirements
Nov 2010
ICH Q7 Guidelines and Practical Approaches to Manufacturing APIs - Webinar by GlobalCompliancePanel
Oct 2010
Navigating Pediatric Trials from recruitment to successful on-time completion
Oct 2010
The Tougher U.S. FDA - One Year Later
Oct 2010
ComplianceOnline Webinar - GMPs in Biopharmaceutical Development Laboratories
Oct 2010
Validating Radiation Sterilization for medical device industries
Sep 2010
Compiling the Design History File, and Technical File / Design Dossier - Webinar by GlobalCompliancePanel
Sep 2010
The Cosmetic-Cosmeceutical Distinction: Walking the Line in Developing Label Claims - Webinar by GlobalCompliancePanel
Sep 2010
ComplianceOnline Webinar - Medical Device Changes and The 510(k)
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
Signal Detection and Data Mining - Webinar by GlobalCompliancePanel
Sep 2010
Key Modules of an Effective CAPA SOP - Webinar by GlobalCompliancePanel
Sep 2010
Understanding Corrective and Preventive Action, and Elements of a CAPA System - Webinar by GlobalCompliancePanel
Sep 2010
Product Risk Management - ISO 14971 and ICH Q9
Aug 2010
Important Sterilization Information for Product Developers - Webinar by GlobalCompliancePanel
Aug 2010
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