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Showing 216 conferences
Advanced CMC Masterclass - EU
Oct 2024
Global Meet on Pharmaceutics and Drug Delivery Systems (GMPDDS)
May 2024
Comparability for Biologics
Apr 2023
U.S. FDA and EU Medical Device Directive Requirements for DHFs, DMRs, DHRs, and TF/DDs
May 2022
Pharmacokinetics (PK) / Pharmacodynamics (PD) Studies in Drug Discovery and Development
May 2022
Packaging and Labeling in Pharmaceutical Product Development - Best Practices
May 2022
Quality Control Laboratory Compliance - cGMPs and GLPs
Feb 2022
Advanced CMC MasterClass
Feb 2022
Supplier and Contract Manufacturer Management
Jan 2022
Global Conference on Cleaning Validation
Nov 2021
Conference on Laboratory Medicine & Pathology
Apr 2021
Data Integrity: FDA/EU Requirements and Implementation
Jan 2021
Brazil School for Single Particle Cryo-EM
Nov 2020
FDA`s Regulation of Regenerative Medicine including Stem Cell Treatments and Tissue Engineering Training
Oct 2020
Laboratory Inspection and Auditing
Oct 2020
International Conference on Pharmaceutical Analysis & Analytical Chemistry (Pharmaceutical Analysis)
Jul 2020
Issues in Calibrations and Accuracy in Method Validation
Jun 2020
Strategies for Speeding Up Formulation Development
Jul 2019
Basics of Testing Associated with Sterilization Validation and Routine Processing
Jul 2019
Quality Control for Microbiological Media and Reagents
Jun 2019
How to Prepare Yourself for FDA`s on-going Part 11 Inspection Program
Jun 2019
Solving Statistical Mysteries – What does the FDA want
Jun 2019
How to Prepare a Standard Operating Procedure (SOP)?
May 2019
3-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries
May 2019
New Elemental Impurities Tests for Pharmaceutical Products According to the New ICH Q3D and USP 232/233 Guidelines
May 2019
Stability Studies & Estimating Shelf Life
May 2019
Quality Control for Microbiological Media and Reagents
May 2019
Selection and Use of (Certified) Reference Material in Analytical Laboratories
Mar 2019
Water System Biofilm Control and Microbial Monitoring Myths
Mar 2019
Validation and Use of Excel Spreadsheets in FDA Regulated Environments
Feb 2019
Medical Marijuana in the Workplace
Jan 2019
Particulates in Biological Products - Evolving Regulations for Testing in Clinical and Commercial Stages
Dec 2018
GMP Compliance for Quality Control and Contract Laboratories
Oct 2018
cGMPs in the Quality Control Laboratory
Sep 2018
Advancing Pathology for Cancer Diagnosis, Staging and Prognosis
Aug 2018
HPLC Instrument Qualification and Method Validation
Aug 2018
Key Factors to Write an Effective Standard Operating Procedures (SOP) and Work Instructions (WI)
Jul 2018
Laboratory Investigations for Out of Specification Results
Jul 2018
New Revision of USP <1058>: Analytical Instrument Qualification
Jul 2018
Opioid Abuse in the Workplace: Using Effective Drug Testing and Policies to Reduce the Pain of the Painkiller Epidemic
Jul 2018
Sunshine Act Reporting: Clarification for Clinical Research
Jul 2018
Good Documentation Guideline (Chapter <1029> USP)
Jul 2018
Onboarding In A GMP Environment – Best Practices
Jul 2018
Forced Degradation Studies/ Biologics Stability Programs for Biopharmaceuticals
Jul 2018
Deviation Investigation Best Practices: Ensuring Correct Content and Conclusions
Jul 2018
Patients Suing Under HIPAA
Jul 2018
Develop a Compliant Validation Protocol and Analytical Procedures according to the FDA Guidance and USP Good Documentation Practices
Jul 2018
510(k) Documentation Best Practices for Software or Software Enabled Medical Devices
Jun 2018
Water System Investigation `How-To`s` and Example Case Studies
Jun 2018
Biocompatibility Testing; what you need to know
Jun 2018
Does your QC lab do GMP and non-GMP activities?
May 2018
Why and How - Verification of Compendial Methods - USP [1226]
May 2018
Gaining and Re-Establishing Control of Your Cleanroom
May 2018
How to Achieve a Compliant and Effective Cleanroom Design and Facility Validation
May 2018
Auditing Analytical Laboratories for FDA Compliance
May 2018
Analytical Method Validation Under Good Laboratory Practices - GLPs
Dec 2017
Laboratory Instrument Qualification
Oct 2017
21 CFR Part 11 Compliance for Computer Systems Regulated by FDA
Oct 2017
Laboratory Instrument Calibration
Oct 2017
Investigation of Out-Of-Specification Laboratory Results
Sep 2017
Laboratory-Developed Tests: Why does FDA think they can Regulate them, and why do others think they Cannot
Aug 2017
Understanding Aseptic Technique and Cleanroom Behavior
Jul 2017
Laboratory Accreditation: Getting there is just the beginning
Jul 2017
Harmonizing Compliance Requirements for SDS and Labeling Standards - Accounting for Variations that Exist from Country to Country
Jun 2017
Verification or Validation of Methods in Food Microbiology
Mar 2017
Laboratory Inspection Readiness - Implementing GMPS for the Pharmaceutical Laboratory
Feb 2017
Innate Immunity: The line of defence
Nov 2016
Determining Sample Size: How to Ensure You Get the Correct
Nov 2016
HPLC Analytical Method Development and Validation
Nov 2016
Developing antibiotic alternatives: A discussion of new approaches to overcoming antimicrobial resistance
Nov 2016
Good Laboratory Practice Regulations - Introduction and Strategies for Implementation
Nov 2016
Good Laboratory Practices (GLPs) - Comparing and Contrasting with Good Manufacturing Practices (GMPs)
Nov 2016
Vaccine Antigen Delivery: new approaches to vaccine development
Oct 2016
Laboratory Instrument Calibration: Current FDA Regulatory Requirements and Best Practices
Oct 2016
Laboratory Investigation Out-of-Specification Results
Oct 2016
Calibration in the Laboratory
Oct 2016
Sub-visible Particulates in Biological products
Sep 2016
Legal, Regulatory and Policy Issues Related to Computer System Validation as the FDA Regulates Tobacco Products
Sep 2016
Understanding the USP and FDA Functions in the Pharmaceutical Industry
Sep 2016
Medical Record Standards: What Hospitals Should Know About the CMS Hospital CoPs
Sep 2016
Meeting the Toughest Laboratory Accreditation Requirements (Part-2)
Aug 2016
Lyophilization: What you Need to Know, Validation and Regulatory Approaches
Aug 2016
Evolving Regulatory Expectations for Data Integrity in GMP laboratory
Aug 2016
New CMS CoP Regulations for Managing Grievances and Complaints: What Hospitals Should Know about the CMS and Joint Commission and DNV Standards
Aug 2016
Writing Effective SOPs for the GMP Laboratory
Jul 2016
Creating an Effective Lab Safety Program
Jul 2016
Laboratory Management with ISO/IEC 17025:2-Part Series
Jul 2016
Understanding and Implementing an Effective Laboratory Quality Management System to comply with ISO/IEC 17025
Jul 2016
USP <71> Sterility Testing: New Harmonization with International Compendia and Overview
Jul 2016
21 CFR 111 GMP Dietary Supplement Laboratory
Jun 2016
Project Management Essentials: The 8 Keys to Bring Every Project on Time and On Budget (Part-1)
Jun 2016
Analytical Method Validation under Good Laboratory Practices (GLPs)
Jun 2016
Transfer of Analytical Procedures According to the New USP Chapter [1224]
Jun 2016
Validation of a HPLC/UPLC methodology
Apr 2016
Mathematics of Terminal Sterilization - Probability of Survival Approach -vs- Overkill Approach
Mar 2016
Sterile Filtration of Pharmaceutical Products - What you need to know to meet Validation and Regulatory Requirements - By AtoZ Compliance
Mar 2016
Sterilization Processes: The Methods, Parameters and Deficiencies Often Cited
Feb 2016
Cleanroom Monitoring & Maintaining a Quality Environment : Overcoming USP [797] Common Non-Compliance Issues
Jan 2016
Avoiding 12 Most Common Statistical Errors in Clinical Research
Jan 2016
Writing Effective Standard Operating Procedure (SOPs)
Jan 2016
From the ER to the OR - IQCP Compliance for CAP Accredited Hospitals
Jan 2016
Objectionable Microorganisms: Considering the Risk
Dec 2015
Corrections and Removals - Understanding and Implementing the Final Guidance Document
Nov 2015
Differences between Device Research and Drug Research
Oct 2015
Calibration and Qualification in Analytical Laboratories
Sep 2015
The Enigma of a Healthy Diet
Jul 2015
Preparing for the LDT Regulation
Jul 2015
Is it Method Verification or Validation, or Just Semantics?
Apr 2015
Regulatory Affairs in Biosimilars
Mar 2015
Biological Facility Design for Compliance
Mar 2015
Designing Effective and Efficient Extractables or Leachables Studies for Biologics
Mar 2015
Good Laboratory Practices for Food Manufacturing
Mar 2015
Stability Program to Support Shipping and Distribution of Drug Products
Feb 2015
Understanding the pathways of necroptotic cell death, free webinar
Jan 2015
New Requirements for Sponsors and Laboratories for Analyzing Clinical Trial Samples to Meet GCP/GCLP Internationally
Jan 2015
Cosmetics and the Science of Beautiful Skin
Dec 2014
Role of Analytical support during various audits - Regulatory and Non Regulatory
Aug 2014
Verification or Validation of Methods in Food Microbiology
Jul 2014
Epigenetic Mechanisms in Early Mammalian Development
Jan 2014
Robust Corrective And Preventive Action (CAPA)
Nov 2013
510(k) for IVDs
Nov 2013
CLIA (Clinical Laboratory Improvement Amendments) Guidelines on Quality Control and Quality Assessment
Oct 2013
Verification of Compendial Methods According to the Revised USP Chapter <1226>
Oct 2013
Developing and Updating a ``Compliant`` Lab Compliance Plan (Medicare and Medicaid Focus)
Aug 2013
How to Withstand an FDA Audit of your Facility
Apr 2013
Auditing the QC Microbiology Laboratory for FDA Compliance
Apr 2013
Key Factors to develop an effective CAPA system
Apr 2013
Bioanalytical Methods Validation
Mar 2013
Quality Practices for Research and Development (R&D) CMC Laboratories
Mar 2013
Good Laboratory Practices for Food Processing Quality Labs
Feb 2013
Clinical Laboratory Incident Management Plan - GLP and FDA Compliance
Feb 2013
Decoding CLIA (Clinical Laboratory Improvement Amendments) Regulations
Jan 2013
Negotiating Clinical Trial Contracts in a Minefield: The Stark Rule, Anti-kickback Statute (AKS), False Claims Act (FCA) and Medicare Secondary Payer Rule (MSPR)
Jan 2013
Auditing Analytical Laboratories for FDA Compliance
Nov 2012
Practical strategies to Improve Productivity in the Pharmaceutical Laboratory
Nov 2012
Efficient, Effective and Compliant Documentation in the QC Laboratory
Nov 2012
Laboratory Water Systems: Necessary Water Specifications and Validation Challenges
Oct 2012
System Based Inspections - Laboratory Controls
Oct 2012
Risk Assessment-Compliance Using Easy To Fill Out Documentation
Sep 2012
Addressing Impurities in Pharmaceutical Products: Impurities, Degradants, Residual Solvents and Elemental Impurities
Aug 2012
Sterilization as a Benchmark for Cleaning Validation and Control - Webinar By GlobalCompliancePanel
Aug 2012
New QC Based on Risk Management: A Collaboration between CLIA and CLSI
Jul 2012
Ethics and Scientific Misconduct in Regulated Studies
Jul 2012
Chemical Safety and Chemical Hygiene Plans for the Lab Environment
Jul 2012
HPLC Outside the Box: Beating Your Competitors to Market
Jul 2012
HPLC Outside the Box: How to Think Like a Chromatographer
Jul 2012
Managing GLP Studies in Non-GLP Facilities - Webinar By ComplianceOnline
Jul 2012
Good Laboratory Practices for Bioanalytical Laboratories - Webinar By ComplianceOnline
Jun 2012
Understanding and Implementing ISO 17025
Jun 2012
Test Article Management and Characterization for Drugs and Devices - Webinar By ComplianceOnline
Jun 2012
Excel Spreadsheet Validation To Eliminate 483s - Webinar by GlobalCompliancePanel
Jun 2012
Establishing and following Good Clinical Practice (GCP) compliant with the FDA requirements
May 2012
The Hero of Manufacturing Contamination Control - The Microbiology Lab
Apr 2012
Good Documentation Practices for GXPs
Apr 2012
Implementing the New USP Chapter <1224> for Analytical Method Transfer
Mar 2012
Validation of Bioanalytical Methods and Procedures for FDA Compliance
Mar 2012
Method Validation in Drug Development Process - Common Mistakes and Issues
Mar 2012
Leaping into Lab: Everything about Waived Testing
Feb 2012
Validation of Analytical Procedures for Use in the Pharmaceutical Industry
Feb 2012
FDA/EU Compliant Training for Laboratory Personnel
Feb 2012
Does your pharmaceutical lab have GMP and non-GMP functions?
Feb 2012
Annual Best Practice Phase IV studies
Feb 2012
Live Web Seminar Dietary Supplement Regulatory Compliance in the United States: Labeling, Product Claims & Updates from the FDA By compliance2go
Feb 2012
How to prepare for and survive a CLIA inspection - Clinical Laboratories Improvement Act
Feb 2012
Live Web Seminar Design Controls: What to know when it comes to FDA regulated industry? By compliance2go
Jan 2012
Troubleshooting Microbial Excursions in Pharmaceutical and Biotech Operations
Jan 2012
FDA’s New Food Safety Law - What does It mean for everyone in the Global Food Chain
Jan 2012
Live Web Seminar China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations By compliance2go
Jan 2012
FDA Compliant Handling of Out of Trend Results in Pharmaceutical Quality Control
Dec 2011
Proven Root Cause Investigation Techniques for Pharmaceutical Water Systems
Dec 2011
Lyophilization Process Development and Cycle Design
Nov 2011
Cleanroom & HEPA Filter Testing & Certification: An Owners Guide - Webinar by GlobalCompliancePanel
Nov 2011
A Rational Approach to Developing and Troubleshooting Dissolution Methods for a Variety of Purposes
Sep 2011
Stability Testing Training Online
Aug 2011
Review and Implementation of USP <1058> Analytical Instrument Qualification
Aug 2011
Auditing the QC Microbiology Laboratory for FDA Compliance - Webinar By ComplianceOnline
Aug 2011
Bioanalytical Methods Validation - Webinar By ComplianceOnline
Aug 2011
Analytical Test Methods Validation: FDA, ICH and USP Requirements - Webinar By ComplianceOnline
Aug 2011
Using the USP Effectively - Webinar By ComplianceOnline
Jul 2011
Good Documentation Practices for Laboratory Operations - Webinar By GlobalCompliancePanel
Jun 2011
FDA`s New Enforcement of 21 CFR Part 11 - Webinar By GlobalCompliancePanel
May 2011
Gowning Systems Used in Cleanrooms & Controlled Environments - Webinar By GlobalCompliancePanel
Apr 2011
Proficiency Testing: How to Pass with Flying Colors and What to Do If You Don`t
Apr 2011
Designing appropriate product specifications for lyophilized parenteral products
Apr 2011
Calibration and Qualification in Analytical Laboratories - Webinar By GlobalCompliancePanel
Apr 2011
ComplianceOnline Webinar - Why and How - Verification of Compendial Methods - USP [1226]
Apr 2011
Decoding CLIA Regulations: Calibration, Calibration Verification and Method Validation
Apr 2011
How to Prevent or Handle Protocol Deviations and Violations to be GCP and Regulatory Compliant?
Mar 2011
Alternative Food Preservation: Pasteurization - Part 2
Mar 2011
How to reduce EO residuals in medical devices
Feb 2011
Last changes in Canadian ethics regulations for clinical trial
Feb 2011
Practical Laboratory Statistics - Webinar by GlobalCompliancePanel
Feb 2011
Eliminate the Confusion –Annex 13 GMP guide
Feb 2011
Responsibilities of a Principal Investigator in Clinical Trials: What you Must Do to Ensure Trial Compliance
Feb 2011
The CLIA Laboratory Inspection: Failure is not an Option - ComplianceOnline Laboratory Webinar 2010
Jan 2011
How to Vet an IRB: Expose and Fix Problems Before They Threaten Your Trial
Jan 2011
Laboratory Investigations Relating to Sample Re-Analysis: Covering the basics before being called out - ComplianceOnline Laboratory Webinar
Nov 2010
Performing Investigations for Environmental Excursions - ComplianceOnline Biotechnology Training
Nov 2010
How to Use Foreign Trial Data in Your NDA Approval Process
Nov 2010
Good Documentation Practices in a Regulated Environment - Webinar by GlobalCompliancePanel
Nov 2010
ComplianceOnline Webinar - Gamma Sterilizer Validation: Method 1 and VDmax25 per ISO 11137 ()
Oct 2010
ComplianceOnline Webinar - Preparing for and handling FDA Laboratory GMP inspections
Oct 2010
ComplianceOnline Webinar - Importance of Method Validation Protocols and components of MVP in the Laboratory
Oct 2010
The FDA Tripod - Clinical Trial Regulations, Compliance and GCP in Drug Development
Oct 2010
ComplianceOnline Webinar - GMPs in Biopharmaceutical Development Laboratories
Oct 2010
What to Expect in a Food Safety Audit
Sep 2010
Ensuring GCP compliance through quality auditing in clinical trial
Sep 2010
The ICF Process: Tips on Achieving Optimal compliance and Comprehension
Sep 2010
Quality by Design (QbD) and Analytical Methods - Webinar by GlobalCompliancePanel
Sep 2010
The role of Analytical Program to Support Drug Development Process
Sep 2010
Key Factors to Write an Effective Standard Operating Procedure (SOP)
Sep 2010
Verification of Pharmacopeia Methods - Webinar by GlobalCompliancePanel
Sep 2010
Good Documentation Practices for GMP Operations - Webinar by GlobalCompliancePanel
Sep 2010
ComplianceOnline Webinar - Streamline Documentation System in Pharmaceutical Laboratory
Aug 2010
Method Transfer of Analytical Methods - Webinar by GlobalCompliancepanel
Aug 2010
System Based Inspections - The Laboratory Control System
Aug 2010
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