Conferences
Medical Device Software Engineering Conference
Mastering Verification & Validation Challenges for Software as Medical Device as well as Embedded Software by Enhancing Testing Strategies throughout the Product Life Cycle, all while Deploying Agile Methodologies to Software Engineering & Streamlining Quality & Regulatory Compliance
February 25-26, 2020 | San Diego, CA
9th Annual EU Medical Device & Diagnostic Reimbursement & Market Access Conference
Shedding Light onto Coverage Opportunities for Digital Health Products, Analysis of the Impact of MDR on Clinical & Follow-On Impact on Market Access, all while Continuously Optimizing Strategies to Meet Various Payer Expectations & Successfully Achieve Reimbursement
March 24-25, 2020 | Frankfurt, Germany
10th Annual Pharmaceutical Sales Training Conference
Continuously Optimizing Pharmaceutical Sales Training Content & Delivery to Meet Trainees’ Evolving Preferences, Providing Leadership Development Opportunities & Maximizing the Use of Learning Technologies for Enhanced Retention & ROI
March 25-26, 2020 | Chicago, IL
13th Semi-Annual Medical Device and Diagnostic Sales Training and Development Conference: West
Development & Execution of Innovative & Engaging Sales Training & Education Platforms that Further Enhance Selling Skills to Meet the Rising Demand of a Competitive Value-Based Selling Environment through the Leverage of Technology, Tools and Resources which Support Training with Metrics that Drive Forward Return on Investment
March 31 – April 1, 2020 | San Diego, CA
13th Annual Medical Device Clinical Training & Education Conference: West
Tailoring Training Methods & Strategies to Engage Health Care Professionals through Innovative Strategies, Technology & Adaptive Adult Learning Methodologies while Providing Measurable Evaluation on Trainee Retention of Skills, Proficiency & ROI through Value-Driven Metrics
March 31 – April 1, 2020 | San Diego, CA
9th Annual Medical Communications and Dissemination of Scientific Information Conference
Optimizing Scientific Exchange of Product Information through the Employment of Comprehensive Messaging Strategies, Collaboration Best Practices with MSLs, and Development and Utilization Product Specific Scientific Platforms
April 6-7, 2020 | Boston, MA
5th Annual Pharmaceutical and Biotech Medical Affairs Pre-Launch Strategies Conference
Building Awareness & Effectively Unveiling Product Value through Medical Affairs’ Strategic Alignment & Compliant Cross-Functional Collaboration with Corporate Departments, Focus on Real World Evidence to Support Scientific Narrative, & Optimized Publication Strategies to Reach Pre-Launch Excellence
April 8-9, 2020 | Boston, MA
12th Annual EU Medical Device Clinical Research Conference
Ensuring a Timely & Efficient Approach to Final Steps in Transitioning to MDR Compliant Clinical Strategies Including a Strong Focus on PMCF Requirements, all while Establishing Defined Study End-Points to Optimize Trial Design, Budgeting & Generation of Relevant Quality & Volume of Data
April 22-23, 2020 | Amsterdam, NL
Pharmaceutical Risk Based Clinical Quality Assurance Conference
Developing Robust Clinical Trial Protocols through Standardization of Data Driven Risk Assessment Models, Adequate CRO Oversight & Proper Documentation Practices to Match Regulatory Expectations & Ensure Quality by Design throughout the Clinical Trial Process
April 23-24, 2020 | San Diego, CA
Food & Beverage E-Commerce Operations Conference
Strengthening Food and Beverage E-Commerce Operations in Alignment with Consumer Trends by Harnessing New Technologies to Closely Connect with Customers, Streamline Supply Chains and Fulfillment Processes, and Optimize Sales in the Online Environment
April 28-29, 2020 | Chicago, IL
9th Annual Medical Device Supplier Quality Assurance Conference
In order to ensure the highest quality devices, medical device manufacturers must assess each supplier based on a determined level of risk and qualify parts prior to procurement. Due to a variety of suppliers…
April 28-29, 2020 | Arlington, VA
Pharmaceutical Supply Chain Conference
Aligning Supply Chains with DSCSA Traceability & Serialization Requirements, Navigating Volatility in Trade Policy and Tariff Impact and Utilization of Technology to Streamline Logistics, Operations and Heighten Transparency Across the Pharmaceutical Industry
April 29-30, 2020 | Atlanta, GA
10th Annual Medical Device and Diagnostic Labeling Conference
Streamlining & Optimizing Labeling Strategy in a Rapidly Evolving International Regulatory Environment with a Focus on Developing EU MDR & IVDR Compliant Labels, all while Enhancing Localization & Translation Processes, with the Goal of Reaching Operational Excellence through the Implementation of Impactful ELS, CMS & MDM Technology
May 6-7, 2020 | Chicago, IL
10th Annual Medical Device Packaging Conference
Exploring Robust Testing Methods of Medical Device Packaging, Reviewing Updates and Impact of ISO 11607 and EU MDR, Developing Confident Sampling Plans that Meet FDA Expectations, while Incorporating End User Feedback for Medical Device Packaging Design
May 6-7, 2020 | Chicago, IL
14th Semi-Annual Medical Device Clinical Training and Education Conference: East
Tailoring Training Methods & Strategies to Engage Health Care Professionals through Innovative Strategies, Technology & Adaptive Adult Learning Methodologies while Providing Measurable Evaluation on Trainee Retention of Skills, Proficiency & ROI through Value-Driven Metrics
May 12-13, 2020 | Charlotte, NC
14th Semi-Annual Medical Device and Diagnostic Sales Training and Development Conference: East
Refocusing on The Importance of Good Salesmanship & Increasing Training Efforts to Expand Product Knowledge to Fit the Needs of the Customer in the Rising Demand of a Value Based Selling Environment, Through the Leverage of Interactive Training Methods & Sales Training Technologies
May 12-13, 2020 | Charlotte, NC
6th Annual Medical Device Corporate Strategy and Business Development Conference
Business Development Strategy Standardization Methods & Metrics for Optimal Deal Evaluation Moving Beyond Traditional M&A: Innovative Partnerships & Collaborative Structures to Enhance Expansion Risk-Based Approach to Corporate Growth through Analysis of Recent Changes to the Healthcare Market
September, 2020 | TBD
2nd Annual Life Science Digital Transformation Conference
Optimizing Digital Transformation Initiatives to Reach Defined Objectives, Effectively Engaging with Stakeholders to Lead an Organization-Wide Cultural Shift, all while Focusing Digitalization Efforts on Greater Consumer Data Collection & Processing Capabilities
May 19-20, 2020 | Chicago, IL
9th Annual Pharmaceutical Regulatory Operations and Submissions Conference
Optimizing the Development of Product Approval Submission Dossiers through the Implementation of New Technological Capabilities, Strategies for Increased Content Re-Use within Global Regulatory Operations and Continued Collaboration with External Vendor Partner
June 25-26, 2020 | Boston, MA
2nd Annual Combination Product Regulation Conference
Maintaining Compliance with Updated FDA Expectations and International Regulatory Requirements, while Collaborating throughout the Submission Process to Ensure Approval of Drug & Device Constituents, and Considerations for Post Market Reporting Requirements
June, 2020 | Arlington, VA
5th Annual Life Science Ethics and Compliance Training Conference
Reducing Compliance Risks through Effective Training Programs and Developing Specific Content Relevant to Each Internal Function and the Overall Organization, while Utilizing Available Resources to Design Innovative Courses in a Cost-Effective Manner
June, 2020 | Chicago, IL
Medical Device Biocompatibility Conference
Recent updates to the ISO 10993 standards governing biocompatibility have within the course of a decade revolutionized the framework according to which a thorough biological evaluation
June 23-34, 2020 | Alexandria, VA
3rd Annual Pharmaceutical Portfolio Strategy and Management Conference
Aligning Asset Strategy & Operational Management to Ensure a Balanced Portfolio of Strong Product Candidates which Complement Commercial Offerings and Support the Overall Corporate Strategy through Optimized Leverage of Resources and Strategic Decision Making Supported by High-Level Data Analytics
July 15-16, 2020 | Philadelphia, PA
16th Annual Medical Device Coverage and Reimbursement Conference
Aligning Reimbursement Strategies with CMS & Commercial Payer Requirements to Uphold Medical Necessities, Transition from Volume to Value Based Care, Leverage Existing Codes while Overcoming New Code Expectations and Encourage Growth in the Medical Device Industry
July, 2020 | Chicago, IL
4th Annual US EU MDR Implementation Conference
July, 2020 | Arlington, VA
5th Annual Medical Device Cybersecurity Risk Mitigation Conference
Ensuring Compliance with Regulatory Requirements and Industry Standards to Mitigate Cyber Risks and Continuously Improve Medical Device Security in addition to Collaborating and Sharing Responsibility between Health Delivery Organizations and Manufacturers
July, 2020 | Arlington, VA
9th Annual Life Science Strengthening Patient Advocacy Engagement Conference
Elevating Patient Advocacy through Creative, Patient-Centric Approaches to Engage with Advocacy Groups and Patients Directly, Ensuring Integration of the Patient Voice, Deep Levels of Comprehensive Support and Highest Levels of Value and Return on Investment
July, 2020 | Philadelphia, PA
7th Annual Customer Centric Medical Information Conference
Optimizing Medical Information Operations and Inquiry Responses through the Integration of AI and Automation Tools, Evolving the Standard Response Letter and Utilizing Data Analytics to Ensure Impactful Product Message Development
July, 2020 | Boston, MA
2nd Annual Food Label Claims: Risk Management & Substantiation Conference
Strengthening Product Label Claims through the Development of Comprehensive Evidentiary Support, Increasing Consumer Awareness Regarding Ambiguous Claims and Understanding Customer Expectations
September, 2020 | Chicago, IL
2nd Annual Life Science Advertising and Promotion Regulatory Affairs Conference
September, 2020 | Arlington, VA
4th Annual EU IVD Clinical and Regulatory Affairs Conference
With the IVDR compliance date rapidly approaching, diagnostic manufacturing organizations are crafting plans of action to address updated and new requirements in a timely manner…
September, 2020 | Amsterdam, NL
10th Annual Medical Device and Diagnostic Strategic Pricing and Accounts Conference
Establishing & Building Strategic Partnerships with Key Customers, Focusing on Value and Contract Effectiveness with the use of Advanced Pricing Models, Knowledge of Impactful Healthcare Economics, While Overcoming Competition and Transparency with the use of Benchmarking Data
September, 2020 | Charlotte, NC
12th Annual Managed Markets & Account Management Strategies Conference
Securing Optimal Product Formulary Coverage to Ensure Uninterrupted Patient Access with a Thorough Comprehension of Current Drug Review Considerations, Impact of Prescribing Practices on Provider Considerations and Exploring the Effect of Potential Rebated Changes on the Market
September, 2020 | TBD
5th Annual Pharmaceutical Strategic Pricing Conference
Discussing Interpretations and Definitions for Value Based Pricing through Analysis of Forthcoming Rebate Restriction Regulations and International Price Indexing Models with an Emphasis on Transparency
September, 2020 | Philadelphia, PA
11th Semi-Annual EU Medical Device Regulatory Affairs Conference
Focus on the NB Designation Status & Timeline, Rationale for Prioritization of Specific Product Line Compliance with New Rules & Management of Remaining Tasks, all while Addressing Ongoing MDR Uncertainties in Finalizing the Updated Regulatory Strategy
September, 2020 | Brussels, Belgium
2nd Annual Pharmaceutical & Biotech Gross-to-Net Conference
Increasing Accuracy of Gross-to-Net Forecasts through High Quality Data, Use of Automation & Technology, Alongside Greater Partnerships with Internal & External Stakeholders, Creating Transparency & Precision in Calculating Accruals, Rebates and Ensuring Forecast Accuracy
October, 2020 | TBD
6th Annual Global Pharmaceutical Regulatory Affairs CMC Conference
Employing Comprehensive Product Lifecycle Management Strategies such as Continued Monitoring of ICH Standards and Regulatory Requirements through to Stringent Supply Chain Change Control Processes to Ensure Compliant Pre-Market and Postmarket CMC Operations
October, 2020 | Philadelphia, PA
14th Semi-Annual IVD Clinical & Regulatory Affairs Conference: East
Navigating a Changing US and International Regulatory and Clinical Landscape to Ensure Compliance while Designing Novel IVD Tests, Companion Diagnostics, and New Biomarker Developments as well as Innovating throughout the Industry to Include Wearable Technology and Machine Learning in Tests
October, 2020 | Arlington, VA
2nd Annual EU Medical Device Post-Market Clinical Evaluation Planning Conference
Developing & Implementing Robust Plans to Gather Compliant Post-Market Clinical Follow-Up Data, Practically Defining Clinical Evidence Based on Device Class & Acceptable Information, all while Sharing Solutions to Operational Challenges in Cost-Effective Data Collection
October, 2020 | Frankfurt, Germany
5th Semi-Annual Medical Device Human Factors & Usability Conference: East
Aligning Human Factors & Usability Studies with Expanding Requirements including the Lifecycle of FDA Regulatory Documentation, CE Mark Changes in Light of EU MDR and ISO 62366, Designing and Conducting Comprehensive and Coherent Studies that Provide Accurate Use Data all while Propelling User Needs into the Forefront of Design & Development
October, 2020 | Arlington, VA
8th Semi-Annual Medical Device Sterilization Conference: East
Industry Collaboration & Consensus on Ethylene Oxide Residual Reduction, Risk-Based Approaches to Selection & Validation of Sterilization Modality to Meet Increasingly Complex Regulatory Requirements including FDA Parametric Release, Numerous ISO Standards and EU MDR
October, 2020 | Arlington, VA
8th Annual Medical Device Product Management Conference
Instilling Comprehensive Road Mapping Tools for Heightened Portfolio Success to Lead Strategic Launch Initiatives and Evolve in an Ever-Changing Landscape while Forecasting Trends with AI Based Products
October 27-28, 2020 | Chicago, IL
2nd Annual EU MDR: Quality System Alignment Conference: Chicago
Implementing Effective and Compliant Quality Management Procedures under the EU MDR through Analysis of Post Market Regulatory Requirements, Risk Mitigation throughout the Supply Chain and Increased Economic Operator Oversight
November, 2020 | Chicago, IL
3rd Annual Life Science Regulatory Intelligence & Strategy Conference
Ensuring Regulatory Compliance through Efforts to Shape Global and US Emerging Regulatory Requirements while Collecting and Distributing Relevant Intelligence to Support Product Strategy and Secure Rapid Regulatory Approval
November, 2020 | Arlington, VA
12th Semi-Annual EU Medical Device Regulatory Affairs Conference
Focus on the NB Designation Status & Timeline, Rationale for Prioritization of Specific Product Line Compliance with New Rules & Management of Remaining Tasks, all while Addressing Ongoing MDR Uncertainties in Finalizing the Updated Regulatory Strategy
November, 2020 | Brussels, Belgium
5th Annual EU Medical Device and Diagnostic Quality Management Conference
Ensuring QMS Preparedness in Light of the MDR & IVDR with a Focus on Economic Operator Compliance, Enhanced Supplier Control & Optimal Design of a Robust PMS Strategy, Successfully Managing International Audit Readiness, all while Digitalizing QMS Processes & Data
December, 2020 | Frankfurt, Germany
5th Annual Dietary Supplement Regulatory Strategy Conference
Navigating Regulatory Compliance for Dietary Supplements through NDI Filling Procedures and Appropriate Claims Substantiation, Reviewing the Current Status of CBD Regulations, and Analyzing Consumer Trends Ensuring Safe and Effective Supplement Distribution
December, 2020 | Arlington, VA
9th Semi-Annual Medical Device Sterilization Conference: West
Industry Collaboration & Consensus on Ethylene Oxide Residual Reduction, Risk-Based Approaches to Selection & Validation of Sterilization Modality to Meet Increasingly Complex Regulatory Requirements including FDA Parametric Release, Numerous ISO Standards and EU MDR
December, 2020 | San Diego, CA
17th Semi-Annual Diagnostic Coverage & Reimbursement Conference: East
Practical Interpretation of Increasingly Differing Payer Requirements & Efficiently Reflecting Expectations in Clinical Strategies, Overcoming Challenges in Ensuring Maximum Reimbursement for Established & Novel Tests with the Ongoing Impact of PAMA & Fluctuating Diagnostic Rates, in addition to Grey Areas in Prior Authorization Processes
December, 2020 | Boston, MA
6th Semi-Annual Medical Device Human Factors & Usability Engineering Conference: West
Aligning Human Factors & Usability Studies with Expanding Requirements including the Lifecycle of FDA Regulatory Documentation, CE Mark Changes in Light of EU MDR and ISO 62366, Designing and Conducting Comprehensive and Coherent Studies that Provide Accurate Use Data all while Propelling User Needs into the Forefront of Design & Development
December, 2020 | San Diego, CA
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