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Conferences on Medical laboratories in USA (past events)
Conferences on Medical laboratories
USA
(past events)
Related topics
Clinical Conferences
Laboratory Medicine Conferences
Medical Laboratory Conferences
Showing 289 conferences
BioPharma Clinical Trials Nexus Conference
Oct 2024
Clinical Cytometry Meeting and Course (ICCS)
Oct 2024
Introductory and Advanced Musculoskeletal Ultrasound: Hands-On Diagnostics and Cadaver Lab Based Guided Interventional Skills
Sep 2024
Pharma Anti Counterfeiting & Serialisation
Jun 2024
Lab Ops and Facility Management for Biopharma Summit
May 2024
Digital Health Envision Summit
May 2024
Clinical Trial Billing and Research Compliance Summit
Mar 2024
International Precision Med TRI-CON
Mar 2024
MSACL - The Association for Mass Spectrometry Applications to the Clinical Lab European Congress & Exhibition
Mar 2024
Trial Master File (TMF) Summit
Mar 2024
Bio-IT World Europe Conference & Expo
Nov 2023
Next Generation Gene Therapeutics
Nov 2023
MarketsandMarkets Next-Gen Digital Pathology Conference
Oct 2023
International Conference on Neurology and Neuro Disorders
Jun 2023
Clinical Autonomic Disorders: Case-Based and Laboratory Workshop
May 2023
PEGS Boston Conference & Expo
May 2023
International Conference on Immunity and Immunochemistry
Mar 2023
World Congress On Pathology, Microbiology & Clinical Practice
Sep 2022
Integrin-Targeted Drug Development Summit
Sep 2022
Operationalize: Electronic Trial Master Files
Aug 2022
WYN Cardiology Forum
Jul 2022
Annual Assoc. for Mass Spectrometry: Applications to the Clinical Lab (MSACL US)
Dec 2021
Clinical Trial Innovation Summit
Dec 2021
Medical Devices Innovation Programme
Oct 2021
Clinical Performance Metrics and Analytics Summit
Dec 2020
International Conference on Biologics and Biosimilars
Oct 2020
AAPS PHARMSCI 360 - The American Association of Pharmaceutical Scientists Meeting and Exposition
Oct 2020
Clinical Trials Innovation Programme
Oct 2020
Precision in Medical Devices Boston
Oct 2020
Precision in Drug Discovery & Preclinical Summit Boston
Oct 2020
AI-ML Clinical Development
Sep 2020
The A to Z`s of Microbial Control, Monitoring and Validation of Water Systems for Pharmaceuticals, Biologics, Medical Devices, Cosmetics, and Personal Care Products
Sep 2020
Product Selection & Pipeline Optimization for Generics
Sep 2020
World Congress on Stem Cell and Regenerative Medicine
Sep 2020
Disclosure and Transparency for Clinical Data Summit
Aug 2020
Clinical Trials Inspection Readiness Summit
Aug 2020
Global Conference on Pharmaceutics and Pharmacology
Aug 2020
Clinical Regulatory Medical Writing Forum
Jul 2020
Precision in Clinical Trials Boston
Jul 2020
Risk Management in Medical Devices Industry
Jun 2020
How to be Efficient and Compliant with Part 11, Validation, and SaaS/Cloud
May 2020
Biomolecular Condensates Summit
Apr 2020
eyeforpharma Medical Affairs USA
Apr 2020
Medical Device Risk Management A to Z - Best Practices for Effectiveness and Efficiency
Mar 2020
Product Complaints Forum
Mar 2020
Adaptive Clinical Trials Symposium
Mar 2020
Data Integrity: FDA/EU Requirements and Implementation
Mar 2020
T3: Trials, Tech and Transformation
Jan 2020
International Conference on Biochemistry & Biophysics
Dec 2019
HR Life Sciences
Dec 2019
Virtual Clinical Trials Conference
Dec 2019
Biostatistics for the Non-Statistician
Nov 2019
Investigator-Initiated Trials (IIT) Forum
Nov 2019
FDA`s GMP Expectations for Phase IV and -in-Man Clinical Trials
Nov 2019
FDA Scrutiny of Promotion and Advertising Practices
Oct 2019
Annual Drug Discovery USA Congress
Oct 2019
Strategic Partnerships for Drug Repurposing Forum
Oct 2019
Stability Testing Summit
Sep 2019
World Congress: Delivering Therapies to the Clinic Faster
Sep 2019
Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines
Sep 2019
Identify and Manage Data Integrity Issues, CSV and 21 CFR Part 11
Sep 2019
World Congress on Clinical Research and Biomarkers
Sep 2019
American Society of Clincial Pathology (ASCP) Annual Meeting
Sep 2019
Implementing UDI (Unique Device Identification) - Plan Now for Success
Sep 2019
GMP Compliance for Quality Control and Contract Laboratories
Aug 2019
Trial Master File (TMF) Institute - Philadelphia
Aug 2019
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
Jul 2019
Biocompatibility Testing for Medical Devices
Jun 2019
International Conference on Biomedical and Clinical Research
Jun 2019
The Great Plains Laboratory Presents GPL Academy Practitioner Workshops Minneapolis
Jun 2019
The Great Plains Laboratory Presents GPL Academy Practitioner Workshops San Francisco
Apr 2019
The A to Z`s of Microbial Control, Monitoring, Validation and Troubleshooting of Pharmaceutical Water Systems
Apr 2019
Computer System Validation (CSV) and Data Integrity for Clinical Trials Regulated by FDA
Apr 2019
Biosimilars and Follow-On Biologics Americas
Mar 2019
Method Development and Validation for Assays Supporting Testing of Biologics
Mar 2019
Pediatric Clinical Trials Conference
Mar 2019
Immunotherapeutics & Immunomonitoring Conference
Feb 2019
The Great Plains Laboratory GPL Academy Practitioner Workshops
Feb 2019
China & Pacific Rim Markets: Compliance Processes for Life Science Products - Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations
Jan 2019
TMF Plus and eCTD Plus
Dec 2018
Is your Medical Device Software 510(k) Ready?
Dec 2018
Conducting Effective Investigations of Out of Specification and Atypical Laboratory Results
Dec 2018
Qualification and Validation of Laboratory Equipment and Systems for Regulated Industries
Nov 2018
International Kidney Cancer Symposium
Nov 2018
International Conference on Forensic Research & Forensic Chemistry
Nov 2018
International Conference on Decontamination, Sterilization and Infection Control
Oct 2018
Validation and 21 CFR Part 11 Compliance of Computer Systems
Oct 2018
Leveraging the Laboratory : The Power of Outreach
Sep 2018
International Conference on Clinical Pharmacy and Public Health
Sep 2018
21 CFR Part 11 Compliance for Computer Systems Regulated by FDA
Sep 2018
Medical Tubing
Sep 2018
PREDiCT:3D Models Summit
Aug 2018
World Congress on Advances in Analytical and Bio-Analytical Techniques
Jul 2018
World Liver Conference
May 2018
Different requirements for Phase I Investigational Drug Products:
May 2018
International Conference and Exhibition on Pharmaceutics & Novel Drug Delivery Systems
Apr 2018
Clinical Trial Collaborations
Apr 2018
International Conference & Exhibition on Biologics and Biosimilars
Mar 2018
Cannabis Partnerships Congress
Mar 2018
A Risk Based Approach To Data Integrity
Feb 2018
GPL University Practitioner Workshops
Feb 2018
Drug Dissolution Testing and Establishing Plasma Drug Levels in Humans
Feb 2018
Annual Global BioProduction Summit
Feb 2018
Synthetic Lethality Conference
Feb 2018
Verification vs. Validation - Product Process Software and QMS
Jan 2018
Design History Files, Device Master Records and Quality Management System for Medical Device Company - Principles of Lean Documents and Lean Configuration
Dec 2017
Why you Should be Worried about HIPAA
Dec 2017
Regulatory Requirements and Principles for Cleaning Validation
Dec 2017
Laboratory Informatics Summit
Dec 2017
Adverse Events Reporting and Safety Strategies Summit
Dec 2017
Human Subjects Research Seminar: Current Regulations under FDA and HIPAA
Nov 2017
Digital Pathology Congress
Nov 2017
Statistics for the Non-Statistician
Nov 2017
Statistical Methods A Visual Approach
Nov 2017
21 CFR Part 11 Compliance for Computer Systems Regulated by FDA
Nov 2017
Antibodies and Bio Therapeutics Congress
Nov 2017
Annual Summit on Nanomedicine & Its Applications
Nov 2017
World Congress on Embryology and In vitro Fertilization
Nov 2017
Bioequivalence Summit
Oct 2017
Annual Biorepositories and Sample Management Summit
Oct 2017
Annual Partnerships in Clinical Trials US
Oct 2017
Neglected Tropical Diseases Forum
Oct 2017
DMC Optimization Summit
Oct 2017
The Annual Personalized & Precision Medicine Conference
Oct 2017
Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes
Oct 2017
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
Oct 2017
Combination Products
Sep 2017
FierceBiotech Drug Development Forum
Sep 2017
Writing and implementing effective SOP`s
Sep 2017
Computer System Validation - Reduce Costs and Avoid 483s
Sep 2017
International Conference on Clinical Trials
Sep 2017
HIPAA Under Trump - What to expect and How to comply
Aug 2017
World Medical Laboratory Congress & Expo
Aug 2017
The Challenges of an Effective Change Control Program and How to Address OOS Results
Aug 2017
Documenting Software for FDA Submissions
Aug 2017
Biosimilar from Development to Registration
Aug 2017
FDA Legal Writing Skills that Result in Effective Regulatory & Quality Submissions
Aug 2017
Rare Disease Collaboration Summit
Jul 2017
AI Pharma Innovation
Jul 2017
NGS and Clinical Applications Congress: USA
Jul 2017
Post-Compliance Medical Device Regulations and Evolving Reporting Requirements: Complaint Handling, Medical Device Reporting/ eMDR and Recalls and their compliance with UDI`s
Jul 2017
World CDx: Market Access for Precision Medicine
Jul 2017
Trial Protocol Optimization and Design Congress
Jul 2017
GLP Master Practitioner Workshop
Jul 2017
FDA`s Regulation of Regenerative Medicine including Stem Cell Treatments, Tissue Engineering and Gene Therapies
Jul 2017
Understanding the FDA`s Regulation of HCT/Ps and Successful Product Development Strategies
Jul 2017
Supplier Management for Medical Device Manufacturers
Jul 2017
Annual Vaccines + Therapeutics Summit
Jun 2017
Proton Therapy USA
Jun 2017
Laboratory, Medical and Device Performance and Validation following Regulatory and ICH Statistical Guidelines
Jun 2017
Laboratory, Medical and Device Performance and Validation following Regulatory and ICH Statistical Guidelines
Jun 2017
Applying U.S. FDA Laws and Regulations to Each Phase of Total Product Life Cycle (TPLC)
May 2017
Radiation Sterilization of Medical Products - Beyond the Basics
May 2017
Efficient Process Validation Strategies and Validation Master Plan (VMPs) for Medical Devices
May 2017
FDA`s GMP Expectations for Phase I and -in-Man Clinical Trials
May 2017
Extractables & Leachables USA
May 2017
Laboratory, Medical and Device Performance and Validation following Regulatory
May 2017
Tissue Engineering, Biofabrication & 3D-Bioprinting in Life sciences
Mar 2017
Quality Audits for the Medical Device Industry
Mar 2017
CDRH/Payer Summit for Medical Device Executives
Dec 2016
Statistical Methods for Design Verification, Process Validation, and Process Control
Dec 2016
Best Practices for FDA Inspection
Dec 2016
Medical Devices - ISO 13485 - Do you really know what you need to?
Nov 2016
Bullet Proof 510(k) and Latest FDA Proposed Changes to the Process
Nov 2016
Design of Experiments for Process/Product Optimization
Nov 2016
Overcoming Data Integrity challenges in Life Sciences
Nov 2016
Exporting Marketing Channel Audits, Importing Marketing Channel Audits, and Logistics Channel Incoterms Standards
Oct 2016
Fundamental Laboratory Record Keeping and Compliance Issue
Oct 2016
Statistical Methods for Design Verification, Process Validation, and Process Control
Oct 2016
Developing Documents and Records to meet the Requirement of ISO 17025
Oct 2016
FDA Inspection: Do`s and Don`ts
Oct 2016
Why is FDA at my facility, and what do I do during an inspection?
Oct 2016
Medical Devices: US Law, Regulation and Practice
Oct 2016
Risk Analysis and Design of Experiments (DOE) in Process Validation and Development
Oct 2016
Ensure Your Healthcare Compliance Program Reaches Optimal Potential and Protect your Organization
Sep 2016
Investigator Site Files Summit
Sep 2016
Implementing ISO 13485:
Sep 2016
Modern Drug discovery and Development Summit
Sep 2016
Validation and Part 11 Compliance of Computer Systems and Data
Sep 2016
How FDA Trains Its Investigators to Review Sub-Systems for State of Compliance: What You Need to Do to Prepare for a Successful Inspection
Aug 2016
Virus and Pathogen Clearance and Safety in Biologics
Aug 2016
Global Medical Device Regulation
Aug 2016
Organic Acids Workshop - San Jose
Aug 2016
Navigating through Maze of In-vitro Diagnostics (IVD) Regulations: A systematic approach from Regulatory Strategy to Regulatory Approvals in U.S./Europe/Canada
Jul 2016
Best Practices for Safety Reporting in Clinical Trials for Drugs, Biologics and Medical Devices
Jul 2016
Developing Documents and Records to meet ISO 17025 Requirements
Jul 2016
National Neurotrauma Symposium
Jun 2016
BioLogistics Summit
Jun 2016
Best Practices for Safety Reporting in Clinical Trials for Drugs, Biologics and Medical Devices
Jun 2016
Verification vs. Validation - Product Process Software and QMS
Jun 2016
Internal Auditing for the Medical Device Industry
May 2016
Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs)
May 2016
Risk Analysis and Design of Experiments (DOE) in Process Validation and Development
May 2016
CHI`s Patient Recruitment & Site Selection
May 2016
Analytical Instrument Qualification and Validation: Understanding to Prepare for FDA Audits to become Part 11 Compliant
May 2016
Data Quality and Technology in Clinical Trials
Apr 2016
The International Conference on Minimally Invasive Medicine (MIM)
Mar 2016
Project management tools to improve productivity and compliance in Analytical laboratories
Feb 2016
Annual Oncology Clinical Trials
Feb 2016
Good Laboratory Practice Compliance Monitoring Summit
Jan 2016
Product Information for Medicinal Products in the EU
Jan 2016
Navigating Ethics and Law for Mental Health Professionals: Ethical practice; Risk management, and; Professional codes of ethics
Jan 2016
Compliant Clinical Research Conduct: What Every Clinical Research Professional Needs to Know
Jan 2016
Accreditation to ISO/IEC 17025:2005- Getting There is Only Half the Fun!
Dec 2015
Surviving an FDA Inspection: Understand the Do`s and Don`ts and the Ground Rules
Dec 2015
CNS Clinical Trial Forum
Nov 2015
GMP Validation Workshop | Learn to create your own workshop and private sessions
Oct 2015
Big Data in Clinical Development
Oct 2015
Medical Grade Polymers
Sep 2015
Mobile in Clinical Trials
Sep 2015
ISO/IEC 17025:2005 and Laboratory Accreditation
Aug 2015
The Statistics of: Design Verification, Process Validation, and Statistical Process Control
Aug 2015
Applied Statistics for QA, QC, Manufacturing, and Design Control at SFO
Jul 2015
The European Clinical Trial Directive…Plus…European Filings and Registration Procedures
Jun 2015
Quality Assurance for Microbiological Laboratories
Jun 2015
The A to Z`s of Writing and Enforcing Effective SOPs (Standard Operating Procedures)
May 2015
Atlantic Vaccines and Immunotherapeutics Summit
May 2015
Complaint-Handling, MDR and Recall Management
Mar 2015
Using Statistical Methods for ICH Guidelines
Mar 2015
Managing Advanced Research & Development - 2-day In-person Seminar
Mar 2015
Clinical Drug Development and Approval Process
Mar 2015
Catalyses in Drug Discovery Summit
Feb 2015
Regulatory Filing Strategies Summit
Feb 2015
How to design and to interpret a clinical trial in the targeted therapies Era
Feb 2015
Key GMP Systems in Pharmaceutical and Biotech Labs
Feb 2015
Risk-Based Monitoring and the Quality Risk Management of Clinical Trials
Jan 2015
The Evidence-Based Reimbursement Summit
Nov 2014
XY Congress
Nov 2014
CIO Life Sciences Summit
Oct 2014
Global Clinical Trials
Sep 2014
Regulatory Affairs & Compliance Consultant David R. Dills Explores ` Advertising and Promotional Requirements for Drugs and Medical Devices` at San Diego
Sep 2014
Global Medical Device Regulation: US, EU and Canada at Chicago IL
Sep 2014
FDA`s and the U.S. Customs Border Patrol`s Import and Export Control Program
Aug 2014
International Seminar Establishing the swiftest pathway for registration of Biosimilars in USA
Aug 2014
Understanding and Implementing the Medical Device Directive
Jul 2014
Conducting Effective Investigation of Out-of-Specs and Atypical Laboratory Data
Jul 2014
Practical Strategies for Developing Preclinical and Phase I Oral Drug Formulations
Jun 2014
Partnerships in Medical Device Trials Conference
Jun 2014
Sample Prep
May 2014
US-China Pharma
May 2014
Companion Diagnostics: From Biomarker Identification to Market Entry
Apr 2014
Moffitt Pathology Symposium: Practicing Pathology in a Changing World
Apr 2014
Using Statistical Methods for ICH Guidelines
Apr 2014
Polymeric Materials in Medical Device
Apr 2014
ADME PK/TK and Drug Metabolism in Drug Discovery and Development
Mar 2014
CHI`s Implementing and Managing Strategic Alliances (at SCOPE)
Feb 2014
Annual Biomanufacturing Summit
Jan 2014
Sample Prep East
Dec 2013
International summit on GLP, GCP, & Clinical Research
Nov 2013
MD&M Minneapolis Expo & Conference
Oct 2013
Disposable Solutions for Biomanufacturing Summit USA
Oct 2013
Clinical Trial Supply USA
Sep 2013
Mastering Biofilm Control, Monitoring, Validation and Excursion Investigations of Pharmaceutical Water Systems
Jun 2013
Computer System Validation - Reduce Costs and Avoid 483s: 2-day In-person Seminar
Apr 2013
Life Cycle of Orphan Drug Development & Commercialization
Jan 2013
International Conference on Obesity and Weight Management
Dec 2012
International Summit on GMP & GCP: USA, Europe, Japan, Asia Pacific
Dec 2012
Sponsor/CRO Forum on Clinical Systems and Process Integration
Nov 2012
Contamination-Control and Cleaning and Disinfection
Nov 2012
Quality Oversight Of Clinical Vendors
Oct 2012
Optimizing Regulatory Communications and Submissions
Sep 2012
Clinical Trials in Asia (CTA)
Sep 2012
Protein Formulation Development Summit
Sep 2012
Biosimilars
Sep 2012
Annual Clinical Research in Emerging Countries
Aug 2012
Business Development Strategies For Clinical Trials Service Providers
Jul 2012
Obtaining and Marketing Your 510(k) with Today`s FDA, a 510(k) Workshop
Jun 2012
Clinical Trials Supply & Logistics Summit
Jun 2012
The A to Z’s of Microbial Control, Monitoring and validation of Pharmaceutical Water Systems
May 2012
North American Predictive Toxicology Summit
May 2012
Annual What`s New in Anatomic Pathology and Laboratory Medicine
May 2012
DHF, DMR, DHR and TF - Regulatory Documents Explained, and Best Practices for Controlling Them
Apr 2012
IPA Semi-annual Conference on: Cold Chain & Logistics Management
Apr 2012
Good Laboratory Practice (GLP) for Non-Clinical Laboratory Studies - Application and Compliance to Ensure Safety of Biologic Therapeutics and Medical Devices
Apr 2012
World Vaccine Trials Congress
Apr 2012
Addressing the Challenges of Drug Discovery - Novel Targets, New Chemical Space and Emerging Approaches (F1)
Mar 2012
Annual Drug Discovery Partnership: Filling the Pipeline
Oct 2011
Logipharma Boston
Oct 2011
80024480: REWards -- Research Ethics Workshops About Responsibilities and Duties of Scientists (formerly CORE)
Oct 2011
Animal Models and Their Value in Predicting Drug Efficacy and Toxicity
Sep 2011
RFID in Health Care
Sep 2011
80024475: REWards -- Research Ethics Workshops About Responsibilities and Duties of Scientists (formerly CORE) ()
Jul 2011
2-day In-person Seminar - Electronic Records: Effective Approaches that Reduce Costs
Mar 2011
Clinical Supply Chain Optimization
Mar 2011
Annual Clinical Laboratory Educators Conference CLEC
Feb 2011
LabAutomation
Feb 2011
Partnering for Cures
Dec 2010
Recent Advances in Microbial Control
Nov 2010
SEBIO
Nov 2010
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