Conferences on Medical device
USA (past events)

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Showing 517 conferences
Next-Gen MSL Excellence Summit
Nov 2024
Investigator-Initiated Trials
Nov 2024
IEEE Nuclear Science Symposium and Medical Imaging Conference
Nov 2024
PDA Universe of Pre-Filled Syringes and Injection Devices Conference
Oct 2024
BioPharma Clinical Trials Nexus Conference
Oct 2024
Pre Filled Syringes Connect
Sep 2024
Optimizing Hybrid Clinical Trials Summit
Sep 2024
Evolution Summit
Sep 2024
ADC and Radiopharmaceuticals Pharma and Biotech Partnering Summit
Sep 2024
Risk Evaluation and Mitigation Strategies Summit (REMS)
Aug 2024
MedDev eMarketing Summit
Aug 2024
Next Gen Inhalation Delivery Summit
Jun 2024
Medical Device Software Development Summit
May 2024
Clinical Operations and Clinical Trial Supply Chain Strategy Meeting
May 2024
Health Equity in Clinical Trials Congress
May 2024
ISPOR - Annual International Meeting of the International Society for Pharmacoeconomics and Outcomes Research
May 2024
Re:Imagine Medical Device Marketing
Apr 2024
Clinical Trial Billing and Research Compliance Summit
Mar 2024
Trial Master File (TMF) Summit
Mar 2024
Medical Affairs and Scientific Communications Forum
Mar 2024
Interventional Cardiology Skills Enhancement Course
Feb 2024
Next Generation Gene Therapeutics
Nov 2023
World Congress on Cancer Research and Therapy (WCCRT)
Nov 2023
5G Telemedicine Security Conference
Nov 2023
The MedTech Conference
Oct 2023
American Medical Device Summit
Sep 2023
Finance & Accounting for Bioscience Companies
Sep 2023
LSX World Congress - Biotech | Healthtech | Medtech
Sep 2023
International Conference on Pharmaceutical Education and Practice
Aug 2023
Advanced Wound Care Summit US
Jul 2023
Medical Device Manufacturing and R&D Summit
Jun 2023
PEGS Boston Conference & Expo
May 2023
International Conference on Cardiovascular Medicine and Cardiac Surgery
Mar 2023
The Veterinary Drug Approval Process and FDA Regulatory Oversight
Feb 2023
Pharma and Device Packaging and Labeling West Coast
Nov 2022
Field Service Connect
Nov 2022
Clinical Trials Summit
Oct 2022
Injectables Summit
Oct 2022
RAS Targeted Drug Development Summit
Sep 2022
Fierce Biotech Summit
Sep 2022
WYN Cardiology Forum
Jul 2022
Biomarker and Companion Diagnostics Conference
Jun 2022
Combination Products Summit
Jun 2022
European Congress on Vaccines R&D & Vaccination
Mar 2022
Medical Device Biocompatibility and Toxicology
Jan 2022
Clinical Trial Innovation Summit
Dec 2021
Drug Delivery Partnerships
Oct 2021
Point-of-Care Diagnostics, Global Health & Biosensors World Congress
Oct 2021
Global Pharmaceutical and Medical Meetings Summit
Oct 2021
Medical Devices Innovation Programme
Oct 2021
Precision Medicine World Conference Pittsburgh (PMWC)
Sep 2021
Digital Marketing for Medical Devices
Aug 2021
ComplianceOnline Medical Device Summit
Aug 2021
Breakthroughs Conference and Exhibition
Jun 2021
Digital Marketing for Medical Devices West
Apr 2021
Clinical Performance Metrics and Analytics Summit
Dec 2020
Content Marketing for Life Sciences
Dec 2020
FDA/CMS Summit
Dec 2020
Human Abuse Liability and Abuse-Deterrent Formulations
Nov 2020
International Conference on Medical Imaging and Case Reports (MICR)
Nov 2020
Technology Transfer for Biologics Conference
Oct 2020
International Conference on Biopharma and Biotherapeutics
Oct 2020
Clinical Trials Innovation Programme
Oct 2020
RWE, Market Access, Pricing and Reimbursement Americas
Oct 2020
CMO Quality Oversight & Risk Management Summit
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
AI-ML Clinical Development
Sep 2020
Safety Labeling and Packaging Summit
Sep 2020
FDA Audit, Quality Assurance Practices, Responsibilities and Expectations
Sep 2020
Global Forum (GF) on Temperature Controlled Life Sciences Supply Chains
Sep 2020
Xcelerate at Biotech Week Boston
Sep 2020
MedAffairs Leaders Forum USA
Aug 2020
Disclosure and Transparency for Clinical Data Summit
Aug 2020
Clinical Trials Inspection Readiness Summit
Aug 2020
Clinical Trials Inspection Readiness Summit
Aug 2020
Global Conference on Pharmaceutics and Pharmacology
Aug 2020
Biomedical Engineering and Instrumentation Summit (BEIS)
Jul 2020
Precision in Clinical Trials Boston
Jul 2020
Partnering with ACOs and IDNs Summit
Jun 2020
KOL/Thought Leader Engagement and Advisory Boards Summit
Jun 2020
Technical Writing for Pharma, Biotech and Med Devices
Jun 2020
Risk Management in Medical Devices Industry
Jun 2020
Scholars World Healthcare Summit
Jun 2020
Due Diligence Summit for Life Sciences
May 2020
CATCH-UP : Annual Review of Advances in Heart Failure, Mechanical Circulatory Support & Transplantation
May 2020
Maximizing Investigator Meetings
May 2020
Product Complaints Forum
Mar 2020
Medical Device Risk Management A to Z - Best Practices for Effectiveness and Efficiency
Mar 2020
Adaptive Clinical Trials Symposium
Mar 2020
Data Integrity: FDA/EU Requirements and Implementation
Mar 2020
FDA`s New Import Program for - Strict Precision
Mar 2020
Aggregate Spend and Open Payments Conference
Mar 2020
Process Validation Guidance Requirements (FDA and EU Annex 15: Qualifications and Validation)
Mar 2020
Quality and GMP Compliance for Virtual Companies (Pharmaceutical, Medical Device & Biologics Industries)
Feb 2020
FDA`s Medical Device Software Regulation Strategy
Feb 2020
Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices
Feb 2020
Human Factors Engineering and Usability Studies Summit
Feb 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
Multi-Stakeholder Commercial Model Summit
Dec 2019
Biostatistics for the Non-Statistician
Nov 2019
Investigator-Initiated Trials (IIT) Forum
Nov 2019
MedTech Summit US
Nov 2019
eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada
Nov 2019
Managing Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an Inspection
Nov 2019
FDA`s GMP Expectations for Phase IV and -in-Man Clinical Trials
Nov 2019
Medical Tubing US
Nov 2019
Digital Therapeutics Strategic Partnerships Summit
Nov 2019
Managing Your FDA Inspection: Before, During and After
Nov 2019
Strategic Partnerships for Drug Repurposing Forum
Oct 2019
Medical Innovation Summit
Oct 2019
Designing and Sustaining New and Existing Product Stability Testing Program
Sep 2019
Stability Testing Summit
Sep 2019
Human Factors & User Experience for Medical Device Design
Sep 2019
Implementing UDI (Unique Device Identification) - Plan Now for Success
Sep 2019
Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina)
Aug 2019
Trial Master File (TMF) Institute - Philadelphia
Aug 2019
International Conference on Polymers for Advanced Technologies (PAT)
Aug 2019
Plastic and Cosmetic Surgery
Aug 2019
Medical Device Verification & Validation
Jul 2019
Drug Pricing and Reimbursement Stakeholder Summit
Jul 2019
Risk Management in Medical Devices Industry
Jun 2019
Effectively Addressing and Remediating FDA`s Form 483 Findings, Warning Letters and Consent Decree Compliance Issues
Jun 2019
Biocompatibility Testing for Medical Devices
Jun 2019
International Conference on Biomedical and Clinical Research
Jun 2019
Medical Sensors Design Conference
Jun 2019
Annual Biomarker World Congress
Jun 2019
Project Management in Clinical Research
Jun 2019
FDA Recalls - Before You Start, and After You Finish
May 2019
Statistical Techniques for Medical Device Manufacturers
May 2019
Investigational New Drug (IND) & Investigational Device Exemptions (IDE) Applications Preparation and Submission, and Conducting FDA Meetings
Apr 2019
Method Development and Validation for Assays Supporting Testing of Biologics
Mar 2019
Medical Device Safety and Reporting Summit
Mar 2019
FT Digital Surgery Summit
Mar 2019
Good Clinical Data Management Practices
Mar 2019
Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan
Feb 2019
Compliance Risk Management in Medical Devices, Pharmaceuticals, and Combination Products
Feb 2019
OneMedForum San Francisco
Jan 2019
China & Pacific Rim Markets: Compliance Processes for Life Science Products - Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations
Jan 2019
Additive Manufacturing Americas
Dec 2018
Boston Medical Affairs Seminar
Dec 2018
TMF Plus and eCTD Plus
Dec 2018
Is your Medical Device Software 510(k) Ready?
Dec 2018
US 3D Technology in Medicine and Healthcare Summit
Dec 2018
HIPAA Privacy Security - Time to Get Serious
Nov 2018
International Conference On Biomedical & Health Informatics
Nov 2018
Is Your Medical Device Software 510(k) Ready?
Nov 2018
Annual Data, Evidence and Access Summit
Nov 2018
Applied Statistics for Scientists and Engineers
Nov 2018
Japan: Regulatory Compliance Requirements for Life Science Products
Oct 2018
The Next Level of Private Practice - Risk, Referrals, Retention & Resilience
Oct 2018
Uncovering and Managing Successful Post Market Compliance for Medical Devices
Oct 2018
Advanced Imaging Update
Oct 2018
Combination Products
Oct 2018
Combination Products
Oct 2018
Strategies for Improving Effectiveness and Efficiency of your Quality Management System
Oct 2018
Advanced Heart Failure Summit: Anniversary Celebration of Ventricular Assist Device and Heart Transplantation (AHF)
Oct 2018
Validation and 21 CFR Part 11 Compliance of Computer Systems
Oct 2018
Medical Device Technology Exchange (MDTX)
Oct 2018
How FDA Trains Its Investigators and Inspectors to Review Sub-Systems for State of Compliance: What You Need to Do to Prepare for a Successful Inspection
Sep 2018
Software Risk Management
Sep 2018
Hosting FDA Regulatory Inspections
Sep 2018
Statistics for Process and Quality Control
Sep 2018
Medicinal Chemistry Summit: USA
Sep 2018
International Conference on Hepatobiliary & Pancreatic Disorders
Sep 2018
Medical Fluid Bags
Sep 2018
Medical Tubing
Sep 2018
Life Science Knowledge Management Summit
Aug 2018
Medical Device Value Engineering
Aug 2018
Quality by Design for Medical Devices – Essential Techniques
Aug 2018
Statistical Analysis for Product Development
Jul 2018
World Congress on Advances in Analytical and Bio-Analytical Techniques
Jul 2018
Electrocardiography For Practititioners, An Interactive Course for Clinicians
Jun 2018
PharmaCon Expo
Jun 2018
World Pharmacists & Clinical Pharmacy Annual Congress
May 2018
Effective Complaint Handling, Medical Device Reporting and Recalls
May 2018
World Liver Conference
May 2018
Product Recalls Forum
May 2018
Off-Label Regulatory Compliance Congress
May 2018
Root Cause Analysis: Foundation of Investigations and CAPA
May 2018
Different requirements for Phase I Investigational Drug Products:
May 2018
CHI`s Clinical Trial Oversight Summit
May 2018
Managing Your FDA Inspection: Before, During and After
Apr 2018
Annual Peter D. Stevens Course on Innovations in Digestive Care
Apr 2018
The Use of Drug Master Files & Quality Agreements: Understanding and Meeting your Regulatory and Processing Responsibilities
Apr 2018
International Conference and Exhibition on Pharmaceutics & Novel Drug Delivery Systems
Apr 2018
eCTD Submissions of IND/NDA to the US FDA, EU and Canada
Apr 2018
A Risk Based Strategy for the Development & Validation of and Validation of Analytical Methods with a QbD Approach
Apr 2018
Evolution of the Quality Management System - How to go from Surviving to Thriving
Apr 2018
Central Labs & Diagnostics Partnerships Forum
Mar 2018
The DHF, Technical File and Design Dossier - Similarities, Differences and the Future
Mar 2018
Medical Devices Summit
Mar 2018
Central Monitoring Summit
Mar 2018
A Risk Based Approach To IT Infrastructure Qualification & Compliance
Mar 2018
A Risk Based Approach To Data Integrity
Feb 2018
Medical Imaging in Clinical Research
Feb 2018
Cardiac Arrhythmias: Mysteries of Electrophysiology Unraveled
Feb 2018
Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan
Feb 2018
Drug Dissolution Testing and Establishing Plasma Drug Levels in Humans
Feb 2018
Quality Audits for the Medical Device Industry
Jan 2018
Verification vs. Validation - Product Process Software and QMS
Jan 2018
Medical Device Software An Incremental Approach to Risk and Quality Management
Jan 2018
Onsite GCP Review and Update including the all-important `Investigators Responsibility
Jan 2018
FDA`s Software Monsters: Cybersecurity, Interoperability, Mobile Apps and Home Use
Jan 2018
A Risk Based Approach to Testing of Computerized GxP Systems
Jan 2018
Risk Based Project Management for the Life Sciences Industry
Jan 2018
Why you Should be Worried about HIPAA
Dec 2017
Design History Files, Device Master Records and Quality Management System for Medical Device Company - Principles of Lean Documents and Lean Configuration
Dec 2017
Regulatory Requirements and Principles for Cleaning Validation
Dec 2017
Healthcare CyberSecurity Summit
Nov 2017
Human Subjects Research Seminar: Current Regulations under FDA and HIPAA
Nov 2017
Digital Pathology Congress
Nov 2017
international conference on digital pathology and image analysis
Nov 2017
Supplier Management for Medical Device Manufacturers
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
MedTech Commercial Leaders Forum USA
Nov 2017
Annual Summit on Nanomedicine & Its Applications
Nov 2017
Annual Partnerships in Clinical Trials US
Oct 2017
Complaints, Adverse Event Reporting, and Recalls - An Integrated Approach
Oct 2017
DMC Optimization Summit
Oct 2017
International Conference on Clinical and Medical Case Reports
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
Design Controls for Medical Devices - Regulations, Myths, Challenges, and Best Practices
Oct 2017
Design of Experiments (DOE) for Process Development and Validation
Sep 2017
FierceBiotech Drug Development Forum
Sep 2017
International Conference and Expo on Heart Surgery
Sep 2017
Artificial Intelligence Innovation Summit
Sep 2017
Supplier Management in FDA- and ISO-regulated Industry
Sep 2017
Computer System Validation - Reduce Costs and Avoid 483s
Sep 2017
Life Science Investor Relations Forum
Sep 2017
Production and Process Control: Building a Robust System
Sep 2017
Commercialization of Micro, Nano, and Emerging Technologies (COMS)
Aug 2017
Acceptance Sampling - Methods and Applications
Aug 2017
HIPAA Under Trump - What to expect and How to comply
Aug 2017
Documenting Software for FDA Submissions
Aug 2017
FDA Legal Writing Skills that Result in Effective Regulatory & Quality Submissions
Aug 2017
Rare Disease Collaboration Summit
Jul 2017
International Endoscopy Conference
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
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
Proton Therapy USA
Jun 2017
Overview of Device Regulation - FDA
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
Traceability and the Drug Quality and Security Act Conference
May 2017
Auditing for Medical Device and Pharma Companies – A Tool to Reduce Quality and Compliance Risk
May 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
Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices
May 2017
Human Factors and Predicate Combination Products
May 2017
FDA`s GMP Expectations for Phase I and -in-Man Clinical Trials
May 2017
Extractables & Leachables USA
May 2017
Implementing MDSAP (Medical Device Single Audit Program) for Compliance Success
May 2017
Laboratory, Medical and Device Performance and Validation following Regulatory
May 2017
MSL Society ONBOARD TRAINING PROGRAM
Apr 2017
Quality by Design - Essential Techniques for Medical Devices
Apr 2017
Quality Audits for the Medical Device Industry
Mar 2017
Annual Data and Technology in Clinical Trials USA
Feb 2017
Opal Medical Device Summit
Jan 2017
CDRH/Payer Summit for Medical Device Executives
Dec 2016
Hands-On Abdominal Ultrasound Imaging & Doppler Course
Dec 2016
Statistical Methods for Design Verification, Process Validation, and Process Control
Dec 2016
Best Practices for FDA Inspection
Dec 2016
International Conference on Precision Medicine
Dec 2016
Introduction to Bedside Ultrasound Course for Intensivists, Emergency Room Staff, and New Technologists
Dec 2016
BIOMEDevice San Jose
Dec 2016
SANS Healthcare Cyber Security Summit & Training
Nov 2016
International Conference on Endoscopy
Nov 2016
Design of Experiments and Statistical Process Control for Process Development and Validation
Nov 2016
Medical Devices - ISO 13485 - Do you really know what you need to?
Nov 2016
Validating Radiation Sterilization for Medical Products
Nov 2016
Effective and Efficient Internal and Supplier Quality System Auditing for Medical Devices
Nov 2016
CGMP Quality Principles for the FDA Regulated Industries: 2-Day In-Person Seminar
Nov 2016
Hands-On Tactile Breast Ultrasound Imaging & Doppler Course
Oct 2016
Software Design for Medical Devices Summit (SDMD)
Oct 2016
Hands-On Obstetric & Pelvic Ultrasound Imaging and Doppler Course
Oct 2016
Why is FDA at my facility, and what do I do during an inspection?
Oct 2016
Fundamental Laboratory Record Keeping and Compliance Issue
Oct 2016
Developing Documents and Records to meet the Requirement of ISO 17025
Oct 2016
FDA Inspection: Do`s and Don`ts
Oct 2016
Ensure Your Healthcare Compliance Program Reaches Optimal Potential and Protect your Organization
Sep 2016
Supplier Management for Medical Device Manufacturers
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
Global Medical Device Regulation
Aug 2016
Process Validation Guidance Requirements (FDA and EU Annex 15: Qualifications and Validation)
Aug 2016
OIG Work Plans: How They Impact Providers
Aug 2016
Tougher Import Rules for FDA Imports in
Aug 2016
Creating Reader-Focused Technical Documents in FDA Regulated Industries
Aug 2016
FDA Scrutiny of Purchasing/Supplier Controls
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
Marketing Products without Getting Hammered by FDA
Jul 2016
Best Practices for Safety Reporting in Clinical Trials for Drugs, Biologics and Medical Devices
Jul 2016
Polymers & Plastics in Medical Devices
Jun 2016
PFS-Tech
Jun 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
Understanding and Implementing the Medical Device Directive: 2-Day In-person Seminar
Jun 2016
Verification vs. Validation - Product Process Software and QMS
Jun 2016
Marketing Products Without Getting Hammered by FDA
May 2016
Supplier Management for Medical Device Manufacturers
May 2016
PLM Road Map for the High Tech & Medical Device Industries
May 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
Integration of Human Factors into Medical Device Design: FDA and European Commission
Apr 2016
Data Quality and Technology in Clinical Trials
Apr 2016
Electronics New England
Apr 2016
NextMed / MMVR22 (Medicine Meets Virtual Reality)
Apr 2016
Process Validation for Medical Devices: 2-day In-person Seminar
Mar 2016
The International Conference on Minimally Invasive Medicine (MIM)
Mar 2016
Fraud and Abuse in the Sales & Marketing of Medical Devices
Mar 2016
Writing and Enforcing Effective SOPs
Feb 2016
Designing and Monitoring Approvable Medical Device (cardiovascular) Protocols
Feb 2016
Mastering the HIPAA Privacy, Security, and Breach Notification Rules: Coping with Rule Changes, Managing Incidents, Preparing for Audits, and Avoiding Penalties
Feb 2016
HIPAA Upcoming Changes
Jan 2016
Medical Device Complaint Handling
Jan 2016
Managing FDA Inspections from Readiness through Follow Up Responses
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
Good Laboratory Practice Compliance Monitoring Summit
Jan 2016
Basics of US Medical Device Regulation
Dec 2015
RoboUniverse San Diego
Dec 2015
Surviving an FDA Inspection: Understand the Do`s and Don`ts and the Ground Rules
Dec 2015
Mastering Biofilm Control, Monitoring, Validation and Excursion Investigations of Water Systems for Bio/Pharma, Medical Devices, and Cosmetics Industries
Dec 2015
Equipment, Facility, and Process Qualification and Validation - A Simple Top to Bottom Sustainable Approach
Dec 2015
Medical Design & Manufacturing (MD&M Florida)
Nov 2015
Life Science Competition Congress
Nov 2015
Regulatory Crisis Management: Best Practices for Dealing with the Common Crisis Events for the FDA-Regulated Industry
Nov 2015
Medical Design & Manufacturing (MD&M) Chicago
Nov 2015
How to Prepare for, Manage, and Follow-up to an FDA Inspection: Risk-driven Approach
Oct 2015
Air Medical Transport Conference (AMTC)
Oct 2015
GMP Validation Workshop | Learn to create your own workshop and private sessions
Oct 2015
Software Risk Analysis Tools for Medical Devices and Risk Mitigation
Oct 2015
Big Data in Clinical Development
Oct 2015
Human Factors and Design Controls for Medical Devices and Combination Products
Oct 2015
How to Prepare for an FDA Meeting: Making the Most of Pre-IND/IDE, pre-NDA and Other Critical Meetings
Sep 2015
World Congress and Expo on Medical Devices
Sep 2015
Medical Grade Polymers
Sep 2015
Mobile in Clinical Trials
Sep 2015
MEDevice San Diego Conference and Technology Showcase
Sep 2015
Promotion of Biomedical Products: Regulatory Considerations
Aug 2015
Introduction to Medical Combination Products
Aug 2015
The Statistics of: Design Verification, Process Validation, and Statistical Process Control
Aug 2015
Risk Reduction against Regulatory Enforcement by the Investment Advisory Community Panel
Jul 2015
Effective and Efficient Internal and Supplier Quality System Auditing for Medical Devices
Jul 2015
How to get a CLIA Waiver for your Medical Device
Jul 2015
Applied Statistics for Scientists and Engineers at Boston
Jul 2015
Applied Statistics for QA, QC, Manufacturing, and Design Control at SFO
Jul 2015
Cyber Security for Healthcare Summit
Jul 2015
Medical Device Summit West
Jun 2015
Point-of-Care Diagnostics Conference
Jun 2015
Effective Complaint Handling, Medical Device Reporting and Recalls - Avoiding Costly Errors:
Jun 2015
Life Sciences Trainers and Educators Network Annual Conference (LTEN)
Jun 2015
How to Conduct Medical Device Risk Analysis Effectively
May 2015
The A to Z`s of Writing and Enforcing Effective SOPs (Standard Operating Procedures)
May 2015
FDA Inspections: Before, During and After
May 2015
International Conference on Significant Advances in Biomedical Engineering
Apr 2015
Case Studies from the Heart of Manhattan
Apr 2015
annual Government Programs Summit
Mar 2015
Effective Complaint Handling, Medical Device Reporting and Recalls
Mar 2015
Missing Data in Clinical Trials
Mar 2015
Forecasting and Optimization of the Clinical Supply Chain Summit
Mar 2015
Regulatory Compliance for Dietary Supplements in the US, EU and Canada
Mar 2015
Applied Statistics for Scientists and Engineers
Mar 2015
Lean, Six Sigma, Kaizen and QbD Life Science Summit
Mar 2015
Marketing Products Without Getting Hammered by FDA
Mar 2015
Coupon & Co-Pay Strategy, Tracking, and Compliance
Feb 2015
Regulatory Filing Strategies Summit
Feb 2015
Medical Device & Diagnostic Clinical Education Conference
Feb 2015
Medical Device & Diagnostic Sales Training - Conference
Feb 2015
Effective and Efficient Internal and Supplier Quality System Auditing for Medical Devices
Feb 2015
Hands-On Peripheral Venous & Arterial Imaging, Including Vascular Access
Dec 2014
Hands-On Carotid & Vertebral Duplex Imaging
Dec 2014
Wireless Medical Devices Conference
Dec 2014
LifeScience Alley Conference & Expo
Nov 2014
Quality System Regulations for Drugs, Devices, and Tablets and How to generate your DMF
Oct 2014
Outsourcing in Clinical Trials New England
Oct 2014
CIO Life Sciences Summit
Oct 2014
Validate Your Own Excel Spreadsheet Application - Workshop
Oct 2014
Point of Care Diagnostics
Sep 2014
Polymers in Drug Delivery
Sep 2014
Polymers in Drug Delivery Devices
Sep 2014
Global Clinical Trials
Sep 2014
International Conference on Radiology and Imaging
Sep 2014
Global Medical Device Regulation: US, EU and Canada at Chicago IL
Sep 2014
DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements
Aug 2014
Annual Sustaining Effective CAPA Systems
Jul 2014
Understanding and Implementing the Medical Device Directive
Jul 2014
Conducting Effective Investigation of Out-of-Specs and Atypical Laboratory Data
Jul 2014
Understanding FDA and Avoiding Inspections Leading to Warning Letters, Seizures, Injunctions and Prosecutions
Jul 2014
California Healthcare Transactions
Jul 2014
OneMedForum New York
Jun 2014
Global Pharma Manufacturing Summit
Jun 2014
Medical Device Software Risk Management and Assurance Case
Jun 2014
Precision Diagnostics Summit
Jun 2014
Partnerships in Medical Device Trials Conference
Jun 2014
Sample Prep
May 2014
MD and M Texas MedTech Event
May 2014
CHI`s Biologics Formulation & Delivery Summit
May 2014
Companion Diagnostics: From Biomarker Identification to Market Entry
Apr 2014
Polymeric Materials in Medical Device
Apr 2014
Fundamentals of Clinical Outsourcing Certificate Program
Mar 2014
Regulatory Information Management
Feb 2014
Annual Biomanufacturing Summit
Jan 2014
Sample Prep East
Dec 2013
2-day In-person Seminar: Why is FDA at my facility, and what do I do during an inspection?
Dec 2013
Wireless Medical Devices - West
Dec 2013
Medical Device Agreements: M&A, Licensing, Co-Development, and Collaborations
Nov 2013
The Sunshine Act - Have you seen the light?
Nov 2013
Changes to the 510(k) System - Impact on Innovation, Investment, and Business Development: One and a half day In-person Seminar
Nov 2013
Annual FDA Boot Camp Devices Edition
Nov 2013
MD&M Minneapolis Expo & Conference
Oct 2013
Annual Forum on Sunshine Act Compliance & Aggregate Spend Reporting
Oct 2013
Disposable Solutions for Biomanufacturing Summit USA
Oct 2013
Design of Implantable Devices Conference
Sep 2013
Software Validation for the New FDA Inspections
Sep 2013
Clinical Trial Supply USA
Sep 2013
Medical Device Global Labeling Strategies Conference
Jul 2013
Medical Device Manufacturing and R&D Summit
Jun 2013
MedTech Innovate Seminars
Jun 2013
OrthoTec China
Jun 2013
DoD/VA Healthcare
May 2013
Computer System Validation - Reduce Costs and Avoid 483s: 2-day In-person Seminar
Apr 2013
Conducting Successful FDA Meetings to Negotiate Product Development and Approval: 2-day In-person Seminar
Apr 2013
Medical Device Labeling (In-Vitro Lab “Home Brew” off - Label Guidance & Enforcement): 2-day In-person Seminar
Apr 2013
Design of Medical Devices Conference
Apr 2013
The World Congress Annual Leadership Summit On Mergers & Acquisitions (M&A)
Apr 2013
FDA`s Import Requirements and Managing the Import of FDA Regulated Products: 2-day In-person Seminar
Mar 2013
Obtaining Faster FDA 510(k) Approvals - The 510(k) as an Advocacy Document: One and a Half-day In-person Seminar
Mar 2013
Medical Device Summit
Mar 2013
Improve Supplier Quality (for Clinical Trial Projects) - Learn How to Implement a Robust Request for Proposal Process
Feb 2013
Assistive Technologies Industry Association Conference - ATiA
Feb 2013
Annual Health Outcomes and Pharmacoeconomics Research Conference
Jan 2013
Contamination-Control and Cleaning and Disinfection
Nov 2012
Medical Devices Conference: Tools, Technologies, and Strategies to Accelerate Your Time to Market
Nov 2012
An Interactive Workshop on Premarket [510(k)] Notification Submissions
Nov 2012
Quality Oversight Of Clinical Vendors
Oct 2012
Risk Management: ISO14971, IEC62304 and IEC60601-1: 2005 Compliance
Oct 2012
2-day In-person Seminar: CAPA Systems for Medical Device Manufacturers
Oct 2012
2-day In-person Seminar on Statistics for Quality Control and Assurance at New Jersy
Sep 2012
Global Medical Device Regulations - US, EU, Canada, Argentina, Australia, Brazil, India, Japan, Mexico, Russia, South Korea, Taiwan
Sep 2012
Clinical Trials in Asia (CTA)
Sep 2012
Prepare and Submit 510(k) Premarket Notification Submissions for Success
Sep 2012
Annual Clinical Research in Emerging Countries
Aug 2012
One and a Half-day In-person Seminar: FDA Compliant GLP for Nonclinical Studies - For Pharmaceutical and Medical Device Industries
Jul 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
Best Practices in Telehealth and Healthcare Technologies
Jun 2012
Annual Life Sciences Market Research Conference
Jun 2012
2-day In-person Seminar: Medical Device Sterilization: Corrective & Preventive Action
Jun 2012
National Executive Leadership Conference on Breast Centers of Excellence
Jun 2012
China Pharma Landscape and Forecasting Workshop
Jun 2012
Annual Pharmaceutical and Medical Packaging Leadership Summit
Jun 2012
The iMedicine & Mobile Life Sciences World Summit
May 2012
Process Analytical Technology (PAT) is more than it Seems
May 2012
Medical Device Quality Systems, CAPA and European Medical Device regulations
May 2012
Electronics South
May 2012
How to Format Succinct and Comprehensive 510(k)s and PMAs
Apr 2012
DHF, DMR, DHR and TF - Regulatory Documents Explained, and Best Practices for Controlling Them
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
2-day In-person Seminar: Introduction to Design of Experiments for Process Characterization
Apr 2012
Quality Expo Texas
Mar 2012
Application of CAPA to the Device Sterilization Process
Mar 2012
Medical Design & Manufacturing (MD&M Texas)
Mar 2012
IEEE EMBS Forum on Grand Challenges in Biomedical Imaging
Mar 2012
Electronics West
Feb 2012
Life Sciences Internal Audit Forum
Feb 2012
Clear as Mud: Obtaining & Marketing your 510(K) with Today`s FDA
Jan 2012
Annual IEEE Topical Conference on Biomedical Wireless Technologies, Networks, and Sensing Systems (BioWireleSS)
Jan 2012
Global Clinical Budgeting and Contracting Conference
Dec 2011
Navigating 510(k) and PMA Submissions and Approvals
Nov 2011
Clinical Trials for Medical Devices Conference
Nov 2011
Logipharma Boston
Oct 2011
PLASTEC Midwest
Sep 2011
RFID in Health Care
Sep 2011
Annual Global Pricing and Reimbursement for Med Device and Biopharmaceutical Manufacturers
Jun 2011
Medical Electronic Device Conference & Expo – MEDCon
May 2011
Imaging and Signal Processing in Healthcare and Technology - ISPHT
May 2011
National Conference on the FCPA and Anti-Corruption for the Life Sciences Industry
May 2011
Cloud Computer Training: Amazon Web Services for Science & Engineering Boston
Apr 2011
Cloud Computer Training: Amazon Web Services for Science & Engineering Bethesda
Apr 2011
Annual Advances in Arthritis, Arthroplasty and Trauma Course
Mar 2011
Clinical Supply Chain Optimization
Mar 2011
Cloud Computer Training: Amazon Web Services for Science & Engineering San Diego
Mar 2011
Integrating a Quality Management System and Risk Management for Medical Devices Dallas
Mar 2011
Structuring, Negotiating and Managing Life Sciences Collaborative Agreements and Acquisitions
Feb 2011
DesignMed
Feb 2011
Pharma IP Innovations Forum
Feb 2011
Medical Device Patent Litigation
Feb 2011
Annual Scientific Advantage Medical Affairs & MSL Leadership Forum
Jan 2011
The Life Sciences Lawyer`s Guide to
Jan 2011
Clear as Mud: Obtaining and Marketing Your 510(k) With Today`s FDA San Francisco
Jan 2011
Clear as Mud: Obtaining and Marketing Your 510(k) With Today`s FDA Irvine
Jan 2011
Social Media for Pharma
Jan 2011
Medtech 10
Nov 2010
Pharmaceutical Packaging Leadership Summit
Nov 2010
Recent Advances in Microbial Control
Nov 2010
Columbia Business School Annual Healthcare Conference
Nov 2010
SEBIO
Nov 2010
Annual SoCalBio Investor & Partnership Conference
Nov 2010
Medical Product Outsourcing Symposium (MPO)
Nov 2010
Congress of Neurological Surgeons Annual Meeting
Oct 2010
International Symposium on MR-guided Focused Ultrasound
Oct 2010
Phoenix
Oct 2010
RFID in Health Care East
Oct 2010
Medical Device Chief Marketing Officer Summit
Jun 2010
Medical Device Pricing & Reimbursement
Jun 2010

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