Conferences
15th Annual Medical Device Coverage and Reimbursement Conference
Securing Product Reimbursement from CMS & Commercial Payers through Demonstrating Medical Necessity & High Impact Outcomes, Use of Risk Arrangements in Transitioning from Volume to Value-Based Care, Leveraging Existing Codes and Growth in the Medical Device Industry
July 16-17, 2019 | Chicago, IL | Hilton Chicago Magnificent Mile Suites
3rd Annual EU MDR Implementation Conference: Alexandria
Maximizing Remaining Transition Period and Obtaining Product Certification, Development of Adequate Clinical Evaluation Data and Documentation and Clarifying MDR Grey Areas in the Absence of Implementing Acts
July 16-17, 2019 | Alexandria, VA | Hilton Alexandria Mark Center
Life Science Advertising and Promotion Regulatory Affairs Conference
Reducing Risks & Increasing Effectiveness of Advertising & Promotion through Advertising & Promotion Regulatory Oversight, Interpreting & Implementing FDA Guidance on Medical Product Communications That Are Consistent With the FDA-Required Labeling and Guidance on Drug & Device Manufacturer Communications With Payors, Formulary Committees & Similar Entities
July 23-24, 2019 | Alexandria, VA | Hilton Alexandria Old Town
4th Annual Medical Device Cybersecurity Risk Mitigation Conference
Mitigating Cybersecurity Risks through Implementing Regulatory Standards and Industry Frameworks while Increasing Collaboration between Manufacturers and Health Delivery Organizations to ensure Proactive Approaches to Device Security
July 23-24, 2019 | Arlington, VA | Le Meridien Arlington
Medical Device and Diagnostic Sales Enablement Conference
Increasing Overall Efficiency and Effectiveness of Medical Device Sales Teams through Exploration of Internal Commercial Alignment and Communication, Employment of Innovative Technologies for Streamlined Content Delivery and Training, and Promotion Cross Functional Collaboration for Optimal Sales Operations and Future Sales Enablement
July 23-24, 2019 | Chicago, IL | Hyatt Centric Chicago Magnificent Mile Hotel
8th Annual Life Science Strengthening Patient Advocacy Engagement Conference
Enhancing Patient Advocacy Initiatives through an Increased Focus on Diverse Patient Populations and Comprehensive Alliance Building Efforts While Strategizing for Innovative and Improved Access Opportunities, Optimizing Data Circulation and Partnering for Patient Success
July 30-31, 2019 | Philadelphia, PA | Four Points by Sheraton Philadelphia City Center
6th 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 30-31, 2019 | Boston, MA | Doubletree Suites by Hilton Boston – Cambridge
9th Annual Medical Device 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 10-11, 2019 | Charlotte, NC
Food Label Claims: Mitigating Legal & Regulatory Risks Conference
Strengthening Product Label Claims through the Development of Comprehensive Evidentiary Support, Increasing Consumer Awareness Regarding Ambiguous Claims and Understanding Customer Expectations
September 10-11, 2019 | Chicago, IL
4th 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 17-18, 2019 | Philadelphia, PA
11th Annual Managed Markets and 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 18-19, 2019 | New Orleans, LA
9th 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 18-19, 2019 | Brussels, Belgium
Life Science Manufacturing Automation Optimization Conference
Ensuring Robust, Uninterrupted and Compliant Product Supply Chains through Facility Retrofitting to Integrate Industry 4.0 Capabilities and Connected Software Systems, Embracing IoT, and the Utilization of Cutting Edge Instrumentation
September 24-25, 2019 | Charlotte, NC
2nd Annual Life Science Regulatory Intelligence and Strategy Conference
Reducing Risk & Increasing Clearance Certainty through Insightful Regulatory Intelligence & Strategy for Supporting Innovative Study Design Teams to Secure Rapid Product Approval, Expand Indications and Maintain Compliance for Marketed Products
October 2019 | Arlington, VA
Pharmaceutical and 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 16-17, 2019 | Chicago, IL
12th Annual IVD Clinical & Regulatory Affairs Conference: East
Considerations while Navigating Regulatory Pathways for Novel IVD Tests, Companion Diagnostics, & Precision Medicine, Addressing Clinical Trial Design & Validation of Technological Advancements, with Insights on Challenging International Regulations including EU IVDR & Asian Regulatory Pathways
October 22-23, 2019 | Arlington, VA
3rd Semi-Annual Medical Device Human Factors & Usability Engineering 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 22-23, 2019 | Arlington, VA
European 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 29-30, 2019 | Frankfurt, Germany
6th Semi-Annual Medical Device Sterilization Conference: East
Industry Collaboration and Consensus on Ethylene Oxide Residual Reduction, Risk-Based Approaches to Selection and Validation of Sterilization Modality to Meet Increasingly Complex Regulatory Requirements including FDA Parametric Release, Numerous ISO Standards and EU MDR
October 29-30, 2019 | Arlington, VA
5th 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 29-30, 2019 | Philadelphia, PA
4th Annual Dietary Supplement Regulation Conference
Alignment with evolving regulations including USDA National Bioengineered Food Disclosure Law, California’s Proposition 65, FDA quality standards & ongoing substantiation of claims highlighting the utilization of social media & influencers
November 2019 | Arlington, VA
7th Annual Medical Device Product Management Conference
Exploring the Evolution of the Product Manager Role Brought about by the Increase of Global Regulatory Expectations, Strategic Need for Comprehensive Road Mapping Tools and Heightened Importance of Product Launch Initiatives
November 5-6, 2019 | Chicago, IL
Pharmaceutical and Biotech 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 Digitization Efforts on Greater Consumer Data Collection & Processing Capabilities
November 6-7, 2019 | Philadelphia, PA
10th Semi-Annual European Medical Device Regulatory Affairs Conference
Focus on the NB Redesignation 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 13-14, 2019 | Brussels, Belgium
15th Semi-Annual Diagnostic Coverage and 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 3-4, 2019 | Boston, MA
4th Annual EU Medical Device & 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 4-5, 2019 | Frankfurt, Germany
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
December 4-5, 2019 | Chicago, IL
4th 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 10-11, 2019 | San Diego, CA
7th 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 10-11, 2019 | San Diego, CA
13th Semi-Annual IVD Regulatory Affairs Conference: West
Clarification of Regulatory Requirements for Companion Diagnostics and NGS, Insight into the Status of Laboratory Developed Test Specific Policies, all while Strategizing to Ensure Compliance with New European and Asian Market Rules
December 12-13, 2019 | San Diego, CA
Regulatory Information Management Systems Conference
Establishing a Single Authoritative Source of Information, Global Harmonization & Tracking of Regulatory Documentation, Opportunities for Improving Quality & Usability of Regulatory Data, Integration of Multiple Regulatory Technologies into an Aligned System
January, 2020 | Arlington, VA
NGS Laboratory Operations Conference
Trends and Opportunities in NGS Quality, Aligning Lab and Business Objectives in NGS Operations, Reducing NGS Data Processing Time, CMS & FDA Regulations Impacting Varied NGS Tests and Systems
January, 2020 | San Diego, CA
16th Semi-Annual Diagnostic Coverage and Reimbursement Conference: West
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
February 11-12, 2020 | San Diego, CA
13th Semi-Annual Medical Device and Diagnostic Sales Training and Development Conference: West
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
March 31 – April 1, 2020 | San Diego, CA
13th Semi-Annual Medical Device Clinical Training & Education Conference: West
Designing & Executing Innovative, Engaging HCP Training which Incorporates Adaptive Adult Learning Methodologies & Technology to Increase Retention while Providing Measurable Return on Investment which Evaluates Competency, Skills & Proficiency through Value-Driven Metrics
March 31 – April 1, 2020 | San Diego, CA
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
14th Semi-Annual Medical Device Clinical Training and Education Conference: East
Designing & Executing Innovative, Engaging HCP Training which Incorporates Adaptive Adult Learning Methodologies & Technology to Increase Retention while Providing Measurable Return on Investment which Evaluates Competency, Skills & Proficiency through Value-Driven Metrics
May 12-13, 2020 | Charlotte, NC
Forums
Semi-Annual Healthcare Financial Forum: Philadelphia
Rising to the Challenge of a Value-Based Payment Environment | Securing Revenue & Payments in a Varied Reimbursement System | Improving Efficiency & Cost-Effectiveness throughout Healthcare
September 12-13, 2019 | Philadelphia, PA
Semi-Annual Healthcare Revenue Cycle Management Forum: Philadelphia
Streamline Front-End Processes to Ensure Rapid & Accurate Reimbursement in an Evolving Landscape Transitioning from Fee-for-Service to Value-Based Care through Leveraging Internal Resources, Technology and Patient Relations
September 12-13, 2019 | Philadelphia, PA
Semi-Annual Healthcare Revenue Cycle Management Forum: San Diego
Streamline Front-End Processes to Ensure Rapid & Accurate Reimbursement in an Evolving Landscape Transitioning from Fee-for-Service to Value-Based Care through Leveraging Internal Resources, Technology and Patient Relations
October 24-25, 2019 | San Diego, CA
Semi-Annual Healthcare Financial Forum: San Diego
Drive Excellence & Profitability | Translate Strategy into Tactical Operations | Transform Financial Leadership
October 24-25, 2019 | San Diego, CA
Webinars
Regulatory Clarification on Risk Assessment within ISO 13485:2016 Framework
Tuesday, August 6, 2019 – 12:00 PM CDT
Underwriters Laboratories: Healthcare Packaging and Testing to ISO 11607-1 and -2
Tuesday, September 10, 2019 11:00 AM – 11:45 AM CDT
CONTACT US
Q1 Productions
500 N. Dearborn Suite 500
Chicago, IL 60654
T: 312.822.8100
F: 312.873.3969
marketing@q1productions.com
