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Conferences on Medical device in California, USA (past events)
Conferences on Medical device
California, USA
(past events)
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Showing 162 conferences
Aseptic Processing Summit
Oct 2024
Conference & Exhibition - Lyotalk USA
Oct 2024
Evolution Summit
Sep 2024
MedDev eMarketing Summit
Aug 2024
Drug Information Association (DIA) Global Meeting
Jun 2024
STING And TLR-Targeted Therapies Summit
Jun 2024
Clinical Operations and Clinical Trial Supply Chain Strategy Meeting
May 2024
World Congress on Cancer Research and Therapy (WCCRT)
Nov 2023
The MedTech Conference
Oct 2023
Pharma and Device Packaging and Labeling West Coast
Nov 2022
Biomarker and Companion Diagnostics Conference
Jun 2022
ASLMS - The Conference of the American Society for Laser Medicine and Surgery
May 2022
Medical Device Biocompatibility and Toxicology
Jan 2022
Point-of-Care Diagnostics, Global Health & Biosensors World Congress
Oct 2021
Digital Marketing for Medical Devices West
Apr 2021
Clinical Trials Innovation Programme
Nov 2020
Data Integrity: FDA/EU Requirements and Implementation
Mar 2020
FDA`s New Import Program for - Strict Precision
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
HR Life Sciences
Dec 2019
eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada
Nov 2019
Digital Therapeutics Strategic Partnerships Summit
Nov 2019
Partnering with ACOs and IDNs Summit
Oct 2019
FDA Audit, Quality Assurance Practices, Responsibilities and Expectations
Sep 2019
Managing Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an Inspection
Sep 2019
Medical Sensors Design Conference
Jun 2019
Statistical Techniques for Medical Device Manufacturers
May 2019
Method Development and Validation for Assays Supporting Testing of Biologics
Mar 2019
FT Digital Surgery Summit
Mar 2019
Good Clinical Data Management Practices
Mar 2019
The A to Z`s of Microbial Control, Monitoring and Validation of Water Systems for Pharmaceuticals, Biologics, Medical Devices, Cosmetics, and Personal Care Products
Mar 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
Managing Your FDA Inspection: Before, During and After
Dec 2018
Biostatistics for the Non-Statistician
Dec 2018
TMF Plus and eCTD Plus
Oct 2018
Advanced Imaging Update
Oct 2018
International Conference on Biochemistry & Biophysics
Oct 2018
Medical Device Technology Exchange (MDTX)
Oct 2018
Hosting FDA Regulatory Inspections
Sep 2018
Statistics for Process and Quality Control
Sep 2018
Statistical Analysis for Product Development
Jul 2018
Electrocardiography For Practititioners, An Interactive Course for Clinicians
Jun 2018
Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan
Jun 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
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
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
Risk Based Project Management for the Life Sciences Industry
Jan 2018
Regulatory Requirements and Principles for Cleaning Validation
Dec 2017
Applied Statistics for Scientists and Engineers
Nov 2017
21 CFR Part 11 Compliance for Computer Systems Regulated by FDA
Nov 2017
Statistics for the Non-Statistician
Nov 2017
Drug Dissolution Testing and Establishing Plasma Drug Levels in Humans
Oct 2017
Complaints, Adverse Event Reporting, and Recalls - An Integrated Approach
Oct 2017
International Conference on Clinical and Medical Case Reports
Oct 2017
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
Oct 2017
Artificial Intelligence Innovation Summit
Sep 2017
Supplier Management in FDA- and ISO-regulated Industry
Sep 2017
Why you Should be Worried about HIPAA
Sep 2017
FDA`s GMP Expectations for Phase IV and -in-Man Clinical Trials
Aug 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
FDA`s GMP Expectations for Phase I and -in-Man Clinical Trials
May 2017
Human Factors and Predicate Combination Products
May 2017
Overview of Device Regulation - FDA
Apr 2017
Effective Complaint Handling, Medical Device Reporting and Recalls
Mar 2017
Quality Audits for the Medical Device Industry
Mar 2017
BIOMEDevice San Jose
Dec 2016
Medical Devices - ISO 13485 - Do you really know what you need to?
Nov 2016
Validating Radiation Sterilization for Medical Products
Nov 2016
CGMP Quality Principles for the FDA Regulated Industries: 2-Day In-Person Seminar
Nov 2016
Fundamental Laboratory Record Keeping and Compliance Issue
Oct 2016
Developing Documents and Records to meet the Requirement of ISO 17025
Oct 2016
Why is FDA at my facility, and what do I do during an inspection?
Oct 2016
FDA Inspection: Do`s and Don`ts
Oct 2016
HIPAA Privacy Security - Time to Get Serious
Oct 2016
Applying U.S. FDA Laws and Regulations to Each Phase of Total Product Life Cycle (TPLC)
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
Acceptance Sampling - Methods and Applications
Aug 2016
Creating Reader-Focused Technical Documents in FDA Regulated Industries
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
PFS-Tech
Jun 2016
BioLogistics Summit
Jun 2016
Marketing Products Without Getting Hammered by FDA
May 2016
PLM Road Map for the High Tech & Medical Device Industries
May 2016
Internal Auditing for the Medical Device Industry
May 2016
Integration of Human Factors into Medical Device Design: FDA and European Commission
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
Computer System Validation - Reduce Costs and Avoid 483s
Feb 2016
HIPAA Upcoming Changes
Jan 2016
Medical Device Complaint Handling
Jan 2016
Compliant Clinical Research Conduct: What Every Clinical Research Professional Needs to Know
Jan 2016
Basics of US Medical Device Regulation
Dec 2015
RoboUniverse San Diego
Dec 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
How to Prepare for an FDA Meeting: Making the Most of Pre-IND/IDE, pre-NDA and Other Critical Meetings
Sep 2015
MEDevice San Diego Conference and Technology Showcase
Sep 2015
Promotion of Biomedical Products: Regulatory Considerations
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
Medical Device Summit West
Jun 2015
Point-of-Care Diagnostics Conference
Jun 2015
Human Subjects Research Seminar: Current Regulations under FDA and HIPAA
Jun 2015
Software Design for Medical Devices Summit (SDMD)
May 2015
The A to Z`s of Writing and Enforcing Effective SOPs (Standard Operating Procedures)
Apr 2015
Effective Complaint Handling, Medical Device Reporting and Recalls
Mar 2015
Effective and Efficient Internal and Supplier Quality System Auditing for Medical Devices
Feb 2015
Cyber Security for Healthcare Summit
Dec 2014
Wireless Medical Devices Conference
Dec 2014
Point of Care Diagnostics
Sep 2014
Annual Sustaining Effective CAPA Systems
Jul 2014
Validation and 21 CFR Part 11 Compliance of Computer Systems
Jul 2014
California Healthcare Transactions
Jul 2014
Sample Prep
May 2014
Annual Biomanufacturing Summit
Jan 2014
Wireless Medical Devices - West
Dec 2013
2-day In-person Seminar: Why is FDA at my facility, and what do I do during an inspection?
Dec 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
Disposable Solutions for Biomanufacturing Summit USA
Oct 2013
Design of Implantable Devices Conference
Sep 2013
Software Validation for the New FDA Inspections
Sep 2013
Conducting Successful FDA Meetings to Negotiate Product Development and Approval: 2-day In-person Seminar
Apr 2013
Obtaining Faster FDA 510(k) Approvals - The 510(k) as an Advocacy Document: One and a Half-day In-person Seminar
Mar 2013
Improve Supplier Quality (for Clinical Trial Projects) - Learn How to Implement a Robust Request for Proposal Process
Feb 2013
Medical Device Risk Management A to Z - Best Practices for Effectiveness and Efficiency
Jan 2013
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
Risk Management: ISO14971, IEC62304 and IEC60601-1: 2005 Compliance
Oct 2012
Clinical Trials in Asia (CTA)
Sep 2012
2-day In-person Seminar: CAPA Systems for Medical Device Manufacturers
Aug 2012
Obtaining and Marketing Your 510(k) with Today`s FDA, a 510(k) Workshop
Jun 2012
Clinical Trials Supply & Logistics Summit
Jun 2012
2-day In-person Seminar: Medical Device Sterilization: Corrective & Preventive Action
Jun 2012
China Pharma Landscape and Forecasting Workshop
Jun 2012
Process Analytical Technology (PAT) is more than it Seems
May 2012
Good Laboratory Practice (GLP) for Non-Clinical Laboratory Studies - Application and Compliance to Ensure Safety of Biologic Therapeutics and Medical Devices
Apr 2012
Application of CAPA to the Device Sterilization Process
Mar 2012
Electronics West
Feb 2012
Annual IEEE Topical Conference on Biomedical Wireless Technologies, Networks, and Sensing Systems (BioWireleSS)
Jan 2012
Cloud Computer Training: Amazon Web Services for Science & Engineering San Diego
Mar 2011
DesignMed
Feb 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
Annual SoCalBio Investor & Partnership Conference
Nov 2010
Congress of Neurological Surgeons Annual Meeting
Oct 2010
Phoenix
Oct 2010
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