At Informatica Sales Kickoff 2015, Partner Summit, you will: Hear from members of our executive leadership team as they share Informatica’s strategic initiatives, solution focus, and plans to help partners drive more business in 2015. Gain visibility and exposure for your company with the Informatica worldwide sales force at our Partner Connect networking event. Discuss joint selling opportunities to increase your revenue and extend your reach at rotational meetings with Informatica sales management. Build Informatica product knowledge and expand opportunities to grow your business on the Informatica Platform at enablement sessions and rotational meetings with Informatica product management.
HighPoint is a proud Platinum Sponsor of the 2015 Model N Rainmaker Conference. Rainmaker 2015 provides a valuable networking forum and the opportunity to engage directly with executives, power users and managers from companies using Model N Revenue Management systems. The event presents noted industry experts to discuss important emerging trends and offers access to Model N experts in product, services and support areas for scheduled and impromptu meetings. Click here for more information about this event.
This conference will focus on IDMP compliance preparations in Europe before it comes into force on July 2016. Despite the fact the regional implementation guidelines have not been published yet, decisions about the compliance preparations need to be already made today as this legislation has major implications for all companies active in the industry and this means a lot of work to be done in an a very short timeframe. Therefore, this conference will focus on gathering corporate professionals from Regulatory Operations, Regulatory Affairs, Master Data Management, Regulatory Information Systems and other key stakeholder departments who have already started their programmes and projects for IDMP compliance challenge and, thus, will have some lessons learnt and practices to share for those who are less advanced in the journey. Click here for more information about this event.
MDM Day is a full-day workshop where customers and prospects can learn about the Master Data Management (MDM) and Product Information Management (PIM) journeys of our customers and partners, share ideas, and network with other like-minded experts and practitioners. Attendees will leave the workshop with the tools, knowledge and connections they need to increase their success with MDM and PIM. Sessions will include:
Attend Europe’s largest, most respected market access and pricing conference to benchmark your strategic decision making. Learn how to prepare your market access strategy for the ever changing global healthcare market. This is your chance to understand the diverse payer landscape and inform decision making with insight from key payer organizations. An informal meet up with 200 of your peers – what more could you ask for? Click here for more information about this event.
Join HighPoint Solutions and InnoPeritus as we host an all day workshop: Preparing for a Product Launch. Years ago, international launches of drugs were done a certain way, times have changed! Are you ready with your launch checklist?
Contact HighPoint’s Director of Sales in Europe, Frederico Braga, if you would like more information about this event: Frederico.Braga@highpointsolutions.com
Every year, the Pharmaceutical industry leaves $11B of unnecessary revenue on the table, including miscalculating Government Pricing, mismanaging payer incentive rebates, allowing local maverick pricing and discounting, and more. Maria Mangler, Director, Contracts, Pricing and Reimbursement, at TOLMAR Pharmaceuticals, has a truly unique perspective on what it takes for emerging Life Sciences manufacturers to transform Contracts, Pricing and Government Reporting processes. Learn how she successfully drove business-critical transformation projects at Astellas, Actient, Auxilium, and now TOLMAR. Join HighPoint and Model N as they highlight:
IIR’s Government Programs Summit keeps you informed on rapidly changing reporting requirements, and provides the tools to ensure correct pricing calculations to achieve compliance excellence in Government Programs. This event is designed to share collective understanding of each program, including new calculation methodologies, how healthcare reform will impact government programs and a clear view on how the program can work well, with solutions to challenges. Click here for more information about this event.
Eyeforpharma Barcelona is the only place to be for 2015. The global event brings together leading pharma executives to share how you can address the era of customer and patient empowerment with four dedicated tracks:
Bio/pharma manufacturers face significant operational challenges related to the proper management of GPO membership data. With membership numbers exceeding hundreds of thousands and no industry standard for class of trade designations, it is crucial for manufacturers to develop strategies to effectively streamline, verify and manage this data. Join us in March to address these challenges and gain best practices to mitigate membership compliance risk, ensure accuracy in COT designation and optimize data processes. Click here for more information about this event.
The 2015 Annual HIMSS Conference & Exhibition, April 12-16 in Chicago, brings together 38,000+ healthcare IT professionals, clinicians, executives and vendors from around the world. Exceptional education, world-class speakers, cutting-edge health IT products and powerful networking are hallmarks of this industry-leading conference. More than 300 education programs feature keynotes, thought leader sessions, roundtable discussions and e-sessions, plus preconference symposia and workshops. Click here for more information about this event.
Attendees will gain valuable insight about the market from industry experts, learn how other customers are leveraging the HealthRules product suite in their organizations, and hear from HealthEdge executives about the future of the products and the company. All customers are encouraged to attend, as there are tracks geared for business, market and technology that will explore all areas of the HealthRules product suite. Click here for more information about this event.
Click here for more information about this event.
Meaningful Use is almost always under the primary control of a coordinator in the IT department. The MU Coordinator studies the regulations, configures the EHR, and decides when it is time to attest. At attestation time the MU Coordinator partners with a financial resource authorized to update the institution’s (or EP’s) Medicare data on the CMS site to complete the attestation. Is the IT and/or Finance department in the best position to make an informed, critical decision on the reliability of your documentation to stand up to a professional auditor. We assert that a “best practice” is to engage your Internal Audit team to study the regulations and evaluate required documentation. They are trained in the same processes and standards of professional skepticism, audit proof, and independence as the Figliozzi team contracted by CMS. The attestation statement highlights provider responsibility for completeness and accuracy of the attestation data. While an IT person would assume summary reports are correct, an (internal or external) auditor is likely to demand proof. This session will enhance your understanding of:
Speaking – HighPoint’s Jay Fisher, Senior Designer in the product “Meaningful Use Monitor”, supporting 42 hospitals and over 3,000 physicians in the process of managing Meaningful Use, and defending providers against CMS Audit of Meaningful Use.
Are you a CHIME member? Great! In this webinar, join us to learn how Adventist has automated program administration, and created organizational structures to help manage staff size, and implemented a multi-level mock audit program to help assure compliance, all within the short time windows required to attest.Click here for more information about this event.
CBI’s Medicaid and Government Pricing Congress is one of the industry’s largest gatherings of Managers and Executives responsible for Contracts, Pricing, Finance, Accounting and Government Program Compliance. Consistently rated highest for quality of content and practical takeaways, the CBI Congress brings real world topics — including Healthcare Reform, Medicaid Expansion, Gross-to-Net, VA/DoD, TRICARE, 340B and Compliance — all into one forum.
The Veeva Summit is one of the industry’s largest events dedicated to commercial cloud solutions for life sciences. Life sciences professionals and Veeva experts gather in Philadelphia to learn, connect, and share valuable insights on industry trends and best practices in multichannel CRM, content management, and master data management. Summit 2015 will include various tracks and workshops on:
The DIA 2015 51st Annual Meeting is the largest multidisciplinary event that brings together a community of life sciences professionals at all levels and across all disciplines come together each June all with a common goal to foster innovation that will lead to the development of safe and effective medical products and therapies to patients.
DIA 2015 51st Annual Meeting will:
HighPoint Solutions invites you to join us for a Roundtable Discussion and networking Cocktail Hour at Boston’s upscale destination steakhouse, STRIP by Strega. At this Roundtable you will hear from your peers and industry experts at the forefront of Cloud analytics & data management, discuss emerging trends including patient analytics, and discover how you can practically develop a Real Word Evidence data lake. We are very excited to have Doug Walker from Ironwood Pharmaceuticals and Rebecca Cotton from Novartis Pharmaceuticals join HighPoint Solution’s Jeffery Catteau as speakers.
The MAHP Summer Conference is designed to help educate the healthcare providers which include health plan presidents and CEOs, medical directors and quality initiative directors. In addition, other physicians, nurses and administrators from related organizations and the public health field will also be in attendance. Topics will include the health information exchange; Medicare and Medicaid issues; the ongoing transformation of the health care industry, changes in reimbursement, issues in health care access and the exchanges, among others, from both the state and federal perspectives. Click here for more information about this event.
The Information Management “IM” Symposium is an annual event started in 2000, presented and hosted by various Blue Cross and Blue Shield Plan Information Professionals. The purpose is to provide Plan business and technical representatives an opportunity to network and exchange best practices and innovations in the field of information management, information architecture, data warehousing, business intelligence, informatics and analytics with the end result of delivering actionable business value to the Plans through the power of information assets. The IM Symposiums consistently draw a high level of attendees due to continued member input and overwhelming interest. Click here for more information about this event.
This year attendees will gather to discuss and reflect on the latest pricing and market access trends, learn about best business practices and meet Europe’s best experts in pricing and profit optimisation. The EPP Pricing Forum brings together Europe’s leading practitioners and experts to discuss, reflect, network and share their best practices with you! Click here for more information about this event.
Now in it’s 20th year, IIR’s MDRP Summit has continued to be THE authoritative MDRP Event for Everything Government Pricing, Rebates and Regulation. Year after year, MDRP provides unparalleled access to the government regulators creating the rules, the industry leaders interpreting them, and the pharmaceutical executives implementing them. MDRP Chicago is where the industry pauses to attend for three days to get the latest updates and industry practices to navigate the regulatory hurdles, minimize wasted resources and optimize finances. Join us to be part of the largest MDRP event of its kind. Acquire best practices from industry peers to ensure your rebate operations are as effective as possible, maximizing company resources. Click here for more information about this event.
Veeva Summit is the largest event dedicated to commercial cloud solutions for life sciences. With more than 500 industry peers from over 60 different life sciences companies, this complimentary event provides you an opportunity to learn and share best practices, hear about the latest technology trends, discuss the future direction of Veeva solutions, and maximise peer-to-peer networking.
EDM, ERS, and RIM have combined for the 2016 Regulatory Submissions, Information, and Document Management Forum. This forum will cover topics in four tracks: Electronic Regulatory Submissions (ERS), Regulatory Information Management (RIM) Business, RIM Technology, and Electronic Document Management (EDM).
HighPoint’s Director of Life Sciences R&D, Lior Keet, will be speaking in a session covering the topic: MDM Facilitating IDMP Compliance while Aligning with Corporate Data Integration Strategies.
Attend Rainmaker 2016 to learn about the latest trends in Revenue Management, hear from industry thought leaders, share best practices and engage with colleagues and industry luminaries. We look forward to seeing you in Scottsdale next February!
1. Be inspired to grow revenue with actionable insights from industry leaders
2. Exchange ideas and network with peers and industry luminaries
3. Participate in industry-specific workshops focused on learning, innovation, tools and techniques
4. Learn the latest trends and best practices in Revenue Management
5. Enjoy the beauty and sunshine of Scottsdale, AZ
The 7th Annual SCOPE Summit, taking place February 23-25, 2016 in Miami, FL, will offer three stimulating days of in-depth discussions in 12 different conferences, 4 pre-conference workshops and 2 symposia focused on issues related to each aspect of clinical trial planning and management: Data Integration, Feasibility, Site Selection and Management, Patient Engagement, Recruitment and Retention, Mobile Tech, Project Management, Outsourcing, Forecasting, Budgeting and Contracting, Quality (QbD) in Trial Conduct, Risk-Based Monitoring, Post-Marketing Studies, Observational Research, Statistics and Biomarker-Driven Trials.
Attend Europe’s largest, most respected market access and pricing conference to benchmark your strategic decision making. Learn how to prepare your market access strategy for the ever changing global healthcare market and understand the diverse payer landscape and how to inform decision making with insight from key payer organisations.
It’s all about getting the right drug, to the right patient, at the right cost and achieving maximum reimbursement success.
This year’s event will host Informatica’s customers and partners who will share their stories giving you valuable tools to improve business processes. At the summit, you will be able to share ideas, get advice and learn from others, including our highly valued customer success team who can solve your toughest data challenges.
eyeforpharma Barcelona will set the vision for your 2020 plans. As your customer takes charge this meeting will enable you take the steps you need to become their partner of choice. The conference will bring together all key stakeholders, so you can collaborate and identify solutions in order to;
GAIN REAL CUSTOMER INSIGHT. Reinvent your understanding of customer experience with a holistic multichannel solution
DELIVER OUTCOMES. Enhance patient experience by partnering with external stakeholders and facilitating internal cross functionality
SELL VALUE. Engage the busier, more informed customer with impactful face-to-face, remote and digital communication
DEVELOP A NEW CORPORATE CULTURE. Pioneer a progressive internal mind-set promoting collaboration, communication and trust
CBI’s Clinical Systems and Technologies Congress offers the opportunity for clinical executives to gain insight into utilizing technology to enable efficient, cost-effective trials while maintaining data control. With a focus on process and data stewardship, attendees walk away with best practices to streamline trial execution through enabling technology at the sponsor/CRO, research site and patient level.
At the Healthcare User Group 2016 Spring Conference, you will find the agenda allows you the opportunity to network with your colleagues, to share best practices, and to ask questions regarding your DST product, but most importantly develop relationships that broaden your knowledge base and allow you to make a difference in your organization. To be Bigger, Better, Bolder.
Join HighPoint Solutions for a free workshop exploring all that encompasses IDMP compliance. Meet and network with colleagues and experts to discuss practical considerations and hands-on preparation for IDMP readiness.
The 2016 Revitas Life Sciences Summit brings together more than 250 Revitas customers, users, and partners to learn, share best practices, and network with colleagues and industry luminaries. In an industry poised for growth, this event will focus on how organizations can improve outcomes and extract maximum value from their investments – all while remaining compliant as regulations shift and change.
A comprehensive schedule covers complex industry issues and real-world applications of solutions through insightful best practice sessions, thought leadership discussions, hands-on learning opportunities, and interactive user forums. Attendees will learn how to develop and implement a strategy that optimizes contracting and revenue management to improve product performance, safeguard earnings, achieve audit-ready compliance, and improve insights.
The 2016 National Summit is the premier Blue Cross Blue Shield conference of the year, assembling professionals from across the Blue Cross Blue Shield System to share best practices, ideas for growth, gather insights from keynote addresses and breakout sessions and much more. Blue Cross Blue Shield Plan attendees come to learn from the best speakers, and to discuss issues and challenges with industry experts to learn about the latest solutions.
The Life Science industry is poised to realize new value from R&D capabilities and there is potential to collaborate in precompetitive areas. Life Sciences organizations can realize significant savings or losses when onboarding vendor partners. Sponsors must be able to effectively and efficiently manage and analyze vast amounts of information as part of the bid review process to identify the appropriate vendors to support a given clinical development program. However, traditional vendor proposal processes generate heterogeneous data that negatively impacts the Sponsor’s ability to conduct a true vendor comparative analysis.
Our workshop will explore the possibility of how sponsors can better manage information, optimizing the vendor management process.
The highly anticipated Final Rule on Covered Outpatient Drugs has been released by CMS! Join hundreds of your industry counterparts at CBI’s Medicaid and Government Pricing Congress to network, learn and benchmark to align thinking on complex issues and effectively implement Final Rule changes.
Now in its 18th year, this congress is one of the industry’s largest gatherings of Managers and Executives responsible for contracts, pricing, finance, accounting and government program compliance. Consistently rated highest for quality of content and practical takeaways, the CBI Congress brings real world topics — including the Final AMP Rule, 340B, Part B, Gross-to-Net, VA and FSS, Contract Compliance and much more — all into one forum. 2016 is no exception as we look forward to the Congress in May!
At Informatica World, you’ll get all the information and insight necessary to harness one of your organization’s most important assets: data. Choose from 130+ breakout sessions featuring Informatica experts and Informatica customers and partners. Learn about the latest product updates, get an inside view of the Informatica Roadmap, and see live demos of the latest Informatica product features.
The Commercial and Pricing Innovation Forum 2016 (June 1 – June 2, 2016 – Venice, Italy) offers a unique opportunity to get introduced to thought leaders of the Life Sciences Industry. It provides the environment where current and emerging commercial-wide trends can be shared and debated taking into consideration new and recurring challenges faced by the Life Sciences Industry.
This premier event is a unique opportunity for you to exchange with experts and peers and discuss the latest important trends on master data management and information governance for a specific industry-related or management-focused topic. You will also network and learn from Informatica product strategists as well as other customers’ journeys to increase your success with a 360 Data view of customers, products, suppliers and “all things data” which are critical to your business.
Veeva Commercial Summit – one of the industry’s largest events dedicated to commercial and medical affairs solutions for life sciences will welcome over 1,000 life sciences professionals and Veeva experts to Philadelphia to learn, connect, and share valuable insights on industry trends and best practices.
Thousands of pharmaceutical and biotech professionals have benefited from CBI’s annual Commercial Contract & Chargeback Excellence. Now in its 12th year, this long-standing event focuses on ways to improve the wholesaler chargeback, navigate class of trade schema complexities, streamline membership management and optimize contract administration and operations. By illustrating software solutions, case studies and perspectives from leading distribution partners, this conference is a comprehensive forum for pharmaceutical professionals to learn best practices and gain strategies to improve contract operations and considerably reduce revenue leakage.
DIA 2016 is the largest global interdisciplinary event that brings together key thought leaders and innovators from industry, academia, regulatory and government agencies, health, patient, and philanthropic organizations from around the globe – and across all disciplines involved in the discovery, development, and life cycle management of health care products.
The goal of the DIA Annual Meeting is to provide you and your team with a rare opportunity to build on what you already know in the development of new therapies and accelerate efforts to enhance health and well-being. Where else can you meet with people from around the world, share your views and knowledge, experience cross-functional content with real-world application from top speakers in the industry, and network with peers to build new relationships across multiple disciplines?
European pharmacovigilance legislation, updated and amended over the past five years, are targeting 2017 for a series of wide ranging changes to case management and reporting regulations, including electronic reporting with E2B (R3), adoption of IDMP and centralized reporting to the EMA.
Conforming to these new regulations will require pharmaceutical companies to consider organizational, functional and technical changes in the coming months. How far reaching are these regulations and how may your company’s pharmacovigilance group be impacted? Join us on July 21st, 2016 at the EMA Pharmacovigilance Readiness Webinar hosted by HighPoint Solutions to learn more about what your organization needs to do to be ready.
As if being solely responsible for the company’s medical innovation wasn’t a big enough job, today’s Life Sciences R&D professionals are hamstrung with inefficiencies; challenges collaborating with internal and external partners, centrally capturing, accessing and integrating data to name a few.
These challenges are exactly why HighPoint developed the R&D Workbench powered by Salesforce. The first tool, developed in collaboration with AstraZeneca, enabled AZ to retain their institutional memory of the events and decisions that went into every aspect of designing a clinical trial. From patient population, to site selection, comorbidities, and many others, all the data, whether structured or unstructured, was captured, integrated, and centrally accessible to everyone. With this institutional knowledge, AZ now has the mechanism to connect the events, decisions, rational, and results to build on designing future trial designs.
In this upcoming webinar, AstraZeneca will present the organizational challenges faced and the strategic benefits received from the solution along with industry perspectives from HighPoint and Salesforce as well as a preview of other solutions of the R&D Workbench powered by Salesforce.
Throughout the years the EPP Forums have been marked as the #1 must-attend pricing and thought-leadership events in Europe! This 6th EPP Life Sciences Pricing Forum will again be unique and interactive, ensuring a maximum learning and insights-gaining opportunity. Click here for more information about this event.
IIR’s MDRP Summit has continued to be THE authoritative MDRP Event for Everything Government Pricing, Rebates and Regulation. Year after year, MDRP provides unparalleled access to the government regulators creating the rules, the industry leaders interpreting them, and the pharmaceutical executives implementing them. MDRP Chicago is where the industry pauses to attend for three days to get the latest updates and industry practices to navigate the regulatory hurdles, minimize wasted resources and optimize finances. Join us to be part of the largest MDRP event of its kind. Acquire best practices from industry peers to ensure your rebate operations are as effective as possible, maximizing company resources. Click here for more information about this event.
The Information Management “IM” Symposium is an annual event started in 2000, presented and hosted by various Blue Cross and Blue Shield Plan Information Professionals. The purpose is to provide Plan business and technical representatives an opportunity to network and exchange best practices and innovations in the field of information management, information architecture, data warehousing, business intelligence, informatics and analytics with the end result of delivering actionable business value to the Plans through the power of information assets. The IM Symposiums consistently draw a high level of attendees due to continued member input and overwhelming interest.
Blue Cross Blue Shield of Michigan is proud to host the 2016 Information Management Symposium in Detroit September 25-28. Please mark your calendar and plan to attend!
Join Workday customers, partners, press, analysts and leaders for their largest event of the year. Click here for more information about this event.
Join more than 450 pharma and biotech leaders in clinical, regulatory, quality, and IT for two days of learning, sharing and networking. Learn how your industry peers are transforming business processes with the latest innovations and best practices.
Last year’s summit featured speakers from industry leaders such as AbbVie, Acorda Therapeutics, Alkermes, Becton Dickinson, Eli Lilly and Company, Gilead Sciences, inVentiv Health Clinical, Janssen Pharmaceuticals, The Medicines Company, United Therapeutics, and Zoetis.
Join more than 700 life sciences professionals at the Madrid Marriott Auditorium Hotel to hear what’s new in the industry, experience the latest technology trends to improve commercial effectiveness, and share best practices among your peers. This two-day event is dedicated to commercial and medical affairs professionals in the life sciences industry.
The 8th Annual SCOPE Summit, taking place January 24-26, 2017 in Miami, FL, will offer three stimulating days of in-depth discussions in 13 different conferences, 6 pre-conference workshops and 2 symposia focused on issues related to each aspect of clinical trial planning and management: Data Integration, Feasibility, Site Selection and Management, Patient Engagement, Recruitment and Retention, Mobile Tech, Project Management, Outsourcing, Forecasting, Budgeting and Contracting, Quality (QbD) in Trial Conduct, Risk-Based Monitoring, Post-Marketing Studies, Observational Research, Clinical Lab Services, Precision Medicine and Biomarker-Driven Trials.
DIA is proud to present the Regulatory Submissions, Information, and Document Management Forum 2017. This forum was initially three separate DIA meetings: EDM (Electronic Document Management), ERS (Electronic Regulatory Submissions), and RIM (Regulatory Information Management), each with their own unique histories. In 2015, those three meetings were combined into one forum in an effort to represent the end-to-end process of managing regulatory submissions and documents. The response to this approach has been incredibly positive with record attendance in 2016, as it serves as the premier place for the discussion of emerging operational standards, best practices, and the processes for submission, creation, and maximum
use of regulatory information. The forum continues to explore information generated along the drug development continuum life cycle and alignment to ever evolving regulatory and electronic standards.
This premier event is a unique opportunity for you to exchange conversations about the latest trends in master data management and data governance. During this event you’ll hear from Fortune 500 companies about their road to success and how they power their digital transformation with data. Informatica product strategists will share the latest on next generation solutions. Don’t miss this opportunity to join the world’s largest vendor user community for MDM and data governance.
At Data Driven 2017, leading companies and experts in data-driven applications and modern data management join for educational presentations, workshops, hands on test drives, roadmap updates, networking, and lots of fun.
During this interactive session, attendees will gain insight on the latest timelines for IDMP as well as valuable tips to make sure your organization is on the right track for compliance readiness. Rather than simply reacting to IDMP, we will discuss the opportunity to truly transform your regulatory information management.
As digitizing healthcare continues to grab a portion of the strategic IT budgets in organizations, business and IT teams must identify how to mature their digital business capabilities. New digital capabilities have the potential to change how payers conduct business across many different stakeholders, business strategies for digital transformation should have a clear path for improvements and growth opportunities. Join us on April 11th, 2017 as we discuss the following topics:
Defining digital healthcare
Examples of Digital Capabilities
Measuring your Digital Capability Maturity
Evolving your digital strategy and capabilities
Attend Rainmaker 2017 to be inspired to grow revenue with actionable insights from industry leaders and exchange ideas and network with peers and industry luminaries. Participate in industry-specific workshops focused on learning, innovation, tools and techniques and learn the latest trends and best practices in Revenue Management this April.
Digi-Tech Pharma 2017(Pharmaceutical technology conference 2017), will provide a platform to all its participants an opportunity to interact, share and discuss the digitalization of Pharma industry. Digi-Tech Pharma 2017(Pharmaceutical conferences 2017) will allow its participants to discuss the various challenges faced, new strategies, case studies and use of innovative ideas in the field of digital pharma IT. Also, to stay updated on the latest trends in digital, social media and mobile strategies required the overcome the obstructions in the transformation. This Digi-Tech Pharma is a unique platform in the Pharmaceutical Conferences which will allow IT leaders to share their technologies and strategies to help the pharma industries. In the Pharma events 2017, the Digi-Tech Pharma will offer opportunities to encourage partnerships and collaborations.
Access Europe Summit 2017 is the #1 market access meeting place in Europe with AstraZeneca, Novartis, Astellas, Janssen, Lundbeck and more on how they are transforming access, putting the payer at the centre of their companies to drive success.
For too long, market access has been a function. But we need market access to become a practice across the organisation – and it’s now our responsibility to become the voice of the payer, ensuring that everyone from clinical to commercial becomes fluent in speaking the language of reimbursement.
Asembia’s 2017 Specialty Pharmacy Summit will return to Wynn/Encore Las Vegas on Sunday, April 30 to May 3, 2017. This annual event is the largest U.S. conference for the specialty pharmacy industry. It welcomes thousands of attendees including senior executives and key decision makers from pharmacies, pharma/biotech manufacturers, payers, wholesalers/distributors, health systems, consultants, healthcare technology companies and other industry stakeholder organizations.
Veeva Global Commercial and Medical Summit is one of the industry’s largest events dedicated to commercial and medical affairs professionals in life sciences, connecting over 1,300 leaders to learn and share valuable insights on trends and best practices. The 2017 Summit will feature more than 60 sessions and workshops delivered by leaders from more than 50 innovative life sciences companies.
After nearly two decades of arming the bio/pharma industry with practical strategies to tackle the complex nuances of the government pricing arena, CBI’s Medicaid and Government Pricing Congress is back and better than ever. This in-depth event showcases industry models and provides best practices to ensure operational and strategic excellence. Benefit from the opportunity to hear from an unparalleled speaking faculty on pressing issues including the Final AMP Rule, 340B, Part B, Gross-to-Net, VA and FSS, Contract Compliance and much more.
Join us for four strategy-packed days filled with the tools, trends, and topics you need to power your business’ transformation in the data-driven digital age. Bring back value to your organization by exploring best practices, industry perspectives, and real-world use cases that show what’s possible when you use data to your competitive advantage.
Now in its 2nd edition, the World Precision Medicine Congress 2017 is an industry landmark bringing together academia, industry and healthcare to discussand debate key challenges and opportunities within:
Diagnostics | Big Data | Genomics | Infrastructure | Investment | Rare Diseases | Oncology | Neuroscience | Diabetes | Cardiovascular | Respiratory
Running alongside the World Advanced Therapies & Regenerative Medicine Congress 2017, the event will bring together 800 attendees and 150 of the industry’s leading pioneers to share the newest data and insights with you.
Join your pharma and biotech peers in clinical, quality and manufacturing, regulatory, and IT on Tuesday 30 May at the Langelinie Pavillonen in Copenhagen to hear what’s new in the industry, experience the latest technology trends, and share best practices.
Is digital transformation at the heart of your business priorities? Are you looking to lift up your enterprise by turning data into business outcomes?
If this is important to you, you do not want to miss the EMEA MDM 360 Summit where established enterprises as well as industry disruptors will share valuable insight into the challenges they overcame in their journeys to become and maintain leaders in the digital revolution.
Next to that, Informatica’s CPO, Amit Walia, will unveil exciting new solutions from Informatica that will enhance customer experience and data governance.
Defining “digital” in the pharma world is complicated. While pharma has embraced “digital”, what that means exactly varies widely from company to company and even different teams in the same corporation. Only a handful have made leading steps to transform their way of working, launching campaigns, creating portals, and training their teams to engage customers.
Join us in this interactive session as we explore our development of an approach to find answers to this question using biologic drugs as an example of specialty treatments, establish a model which can predict yearly revenues with 86% accuracy and compare the impact different medical and marketing activities have to the financial success of biologic treatments, and share some of our learnings and discuss potential ways to move forward.
In this webinar we’ll discuss the effort and reward associated with MACRA submission method, understanding and modeling Base and Bonus reporting factors for 2017 / 2019, CQM Fine Tuning and improving your CQM Scores.
In today’s pharmaceutical landscape, staying competitive and ensuring maximum market penetration means distributing and contracting your drugs though multiple channels. In doing so, there is always the risk of the customer benefiting from discounts multiple times. In this discussion we will focus on the industry-wide problem of duplicate discounts between Medicaid Claims and 340B Chargebacks and what the challenges to problem resolution are.
More than 500 new bio/pharma products will be launched in 2017 and as executing a comprehensive launch becomes increasingly more complex, it is critical to understand key items when mapping your product plan. A pharmaceutical product launch is one of the most critical moments in a product lifecycle. As the regulatory and commercial environments constantly evolve, it is vital to the success of an organization to adapt new launch strategies and tailor a launch to each product.
CBI’s Bio/Pharma Product Launch Summit is a can’t-miss opportunity to discuss with innovative peers how to successfully launch a product in a highly saturated market and navigate the road map to consumer relevance and commercial success.
Now in its 22nd year, IIR’s MDRP Summit has continued to be THE authoritative MDRP Event for Everything Government Pricing, Rebates and Regulation. MDRP provides unparalleled access to the government regulators creating the rules, the industry leaders interpreting them, and the pharmaceutical executives implementing them.
Over the course of three days, there will be ample opportunity to hear government officials keynote, meet with solution providers, and network with like-minded professionals.