Conferences

 

6th Annual Medical Device Postmarket: Surveillance & Clinical Follow-up Conference

Ensuring Long-term Product Quality and Efficacy through Streamlined Postmarket Surveillance Processes including Integration of eQMS for Complaint Intake, Employment of Stringent Postmarket Cybersecurity Strategies and Proactively Preparing for EU MDR Compliance

January 22-23, 2020 | Alexandria, VA | Hilton Alexandria Mark Center

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 | Hilton Garden Inn San Diego Downtown/Bayside

7th Annual Food Labeling Regulatory Compliance Conference

Ensuring Continued Compliance with FDA Label Requirements amidst a Changing Regulatory and Industry Landscape, while Updating Claims based on Consumer Trends and Employing an Overall Science Based Approach

February 11-12, 2020 | Alexandria, VA

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

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 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

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

10th Annual Medical Device Supplier Quality Conference

Updating Supplier Quality Management Processes to Accommodate Innovative Medical Devices, While Collaborating with Software Vendors and Creating Harmonized Systems to Interface with Suppliers on a Global Scale

April 28-29, 2020 | Arlington, VA

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

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

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

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

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

June, 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

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

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

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

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

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

15th Semi-Annual IVD Clinical & Regulatory Affairs Conference: West

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

December, 2020 | San Diego, CA

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