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Trk 20: Innov Theater [clear filter]
Monday, June 27
 

10:00am

#122: DBMS Consulting/Clinical Ink Innovation Theater: Accelerating Clinical Trial Innovation: Technology Case Studies for Improving Data Collection, Monitoring, and Medical Coding Processes
Limited Capacity seats available

Component Type: Session
Level: Intermediate

Standardization supports efficiency but usually with a lack of flexibility. Make the introduction of new technologies less challenging by limiting the scope of change. Learn how one top 5 pharmaceutical company is replacing EDC with eSource by mapping data into their existing processes and clinical database. Learn solutions for expiring dsNavigator support and how a centralized medical coding model can eliminate coding discrepancies by integrating safety systems with RDC, Rave and InForm via Oracle's TMS.

Chair

DBMS Consulting


Chair
Monday June 27, 2016 10:00am - 10:30am
Exhibit Hall B Pennsylvania Convention Center 1101 Arch Street, Philadelphia, PA 19107 USA

12:15pm

#146: Tata Consultancy Services Innovation Theater: Data Transparency Initiative: An Innovative Solution
Limited Capacity seats available

Component Type: Session
Level: Intermediate

With a growing commitment in the pharma world to data transparency, we require an innovative technology-driven solution using newly developed digital tools to make data and document sharing solutions achievable, scalable, and cost-effective. Metadata analytical algorithms will be used for de-identification and anonymization of data. This will ensure a greater control of the quality and reduction in overall process time.

* Presented by: Helle-Mai Gawrylewski, Sr. Director Regulatory Medical Writing, Janssen R&D. Titusville, NJ, USA
* Supported by: Arghya Chattopadhyay, Vice President, Biostatistics and Statistical Programming, Tata Consultancy Services

Chair

Tata Consultancy Services


Chair
Monday June 27, 2016 12:15pm - 12:45pm
Exhibit Hall B Pennsylvania Convention Center 1101 Arch Street, Philadelphia, PA 19107 USA

1:00pm

#148: PAREXEL Innovation Theater: Balancing Rapid Approval with Demonstration of Value
Limited Capacity filling up

Component Type: Session
Level: Intermediate

Global options for rapid approval and access present significant opportunity in the US, Europe, and now Japan. Yet postapproval demands for value demonstration, along with the diversity of payer and regulatory requirements in these regions, have generated unanticipated challenges. PAREXEL will present unique solutions that leverage the benefits of development acceleration, strategically balanced with clinical evidence and real-world innovations that support reimbursement.

Chair

PAREXEL International


Chair
Monday June 27, 2016 1:00pm - 1:30pm
Exhibit Hall B Pennsylvania Convention Center 1101 Arch Street, Philadelphia, PA 19107 USA

1:45pm

#150: Quintiles Innovation Theater: Evidence Optimization: Fueling Smarter Clinical Development and Value Generation
Limited Capacity filling up

Component Type: Session
Level: Intermediate

Drug development challenges drive the need to translate scientific and therapeutic advances to better outcomes. Maximizing real-world and clinical evidence can shorten cycle times from pipeline to patient. This presentation highlights innovative approaches by integrating evidence alongside scientific expertise, technology and global delivery to:
Design and deliver smarter trials
Accelerate study start-up
Make earlier, more informed decisions
Execute with efficiency
Generate better value from evidence.

Chair

Quintiles Transnational


Chair
avatar for QuintilesIMS

QuintilesIMS

Quintiles Transnational

Monday June 27, 2016 1:45pm - 2:15pm
Exhibit Hall B Pennsylvania Convention Center 1101 Arch Street, Philadelphia, PA 19107 USA

4:30pm

#153: BBK Innovation Theater: Reimagining the Patient Experience Through mHealth Technologies
Limited Capacity filling up

Component Type: Session
Level: Intermediate

mHealth remains one of the most talked about trends in clinical R&D. Yet despite many successes across life sciences and health care, industry-wide adoption lags. Patient-centric strategies are critical to any study’s success, and few efforts are more patient-centric than providing tools to improve patient engagement and enable efficient data collection and sharing. This presentation will offer advice on mHealth engagement strategies and share insights gleaned from real use cases.

Chair

BBK Worldwide


Chair
BW

BBK Worldwide

BBK Worldwide

Monday June 27, 2016 4:30pm - 5:00pm
Exhibit Hall B Pennsylvania Convention Center 1101 Arch Street, Philadelphia, PA 19107 USA

5:15pm

#154: ConvergeHealth by Deloitte Innovation Theater
Limited Capacity seats available

Component Type: Session
Level: Intermediate



Chair

ConvergeHEALTH by Deloitte


Chair
Monday June 27, 2016 5:15pm - 5:45pm
Exhibit Hall B Pennsylvania Convention Center 1101 Arch Street, Philadelphia, PA 19107 USA
  • Audience Intermediate
  • format json
  • Interest Area Clinical Safety & Pharmacovigilance
  • Tags Session
 
Tuesday, June 28
 

9:45am

#206: Covance Innovation Theater: Leveraging Patient Data and Historical Investigator Performance Data to Realize Faster Patient Recruitment
Limited Capacity seats available

Component Type: Session
Level: Intermediate

Patient recruitment and enrollment is one of the most critical opportunities to improve the clinical trial execution process. Twenty to 60 percent of the total clinical development timeline is spent on identifying and recruiting the right patients. Through Covance’s proprietary Xcellerate® knowledgebase with over 175,000 individual investigators and our LabCorp patient database with over 70 million de-identified patients, we are able to leverage the two databases to significantly increase our site optimization towards faster patient enrollment.

Chair

Covance Inc.


Chair
CI

Covance Inc.

Covance Inc.

Tuesday June 28, 2016 9:45am - 10:15am
Exhibit Hall B Pennsylvania Convention Center 1101 Arch Street, Philadelphia, PA 19107 USA

12:00pm

#230: Quintiles Innovation Theater: Transforming Patient Recruitment Through Site and Patient Engagement
Limited Capacity filling up

Component Type: Session
Level: Intermediate

Transforming patient recruitment requires operating with patients in mind from start to finish for better outcomes. Generating awareness and trust is an imperative first step. Then getting patients involved in program and protocol design pre-recruitment also effects study execution. It is also imperative to support sites through proper tools, training, and support. Learn how we’re using innovative solutions and partnerships to transform the way patients impact study success.

Chair

Quintiles Transnational


Chair
avatar for QuintilesIMS

QuintilesIMS

Quintiles Transnational

Tuesday June 28, 2016 12:00pm - 12:30pm
Exhibit Hall B Pennsylvania Convention Center 1101 Arch Street, Philadelphia, PA 19107 USA

12:40pm

#232: PRA Innovation Theater: Transforming EMR to EDC
Limited Capacity seats available

Component Type: Session
Level: Intermediate

Disparate EMR systems and lack of CFR 21-11 compliance have hamstrung efforts streamlining data entry for research. PRA's Predictivv platform reduces the duplicate data entry by transforming EMR to EDC in real time.

"Predictivv is the foundation of PRA and our drive towards evidence driven healthcare and research."

Jane Quigley, Vice President of Medical Informatics

Chair

PRA Health Sciences


Chair
Tuesday June 28, 2016 12:40pm - 1:10pm
Exhibit Hall B Pennsylvania Convention Center 1101 Arch Street, Philadelphia, PA 19107 USA

1:20pm

#233: Veeva Innovation Theater: The Great RIM Throwdown! How Are You Managing Regulatory Events?
Limited Capacity seats available

Component Type: Session
Level: Intermediate

Regulatory professionals were asked to share what their organization does well, and what they do poorly when managing regulatory events like manufacturing changes or health authority requests. We’ve taken their top challenges and tested Veeva Vault RIM to see how it stands up. Can it address standardization, tracking, data quality and lack of metrics? Can it deliver local market visibility in three clicks or less? Come see for yourself.

Chair

Veeva Systems


Chair
VS

Veeva Systems, Inc.

NA
Veeva Systems Inc. is a leader in cloud-based software for the global life sciences industry. From compliant promotional content management to best-in-class multichannel marketing, Veeva provides innovative marketing solutions to more than 200 pharmaceutical and biotech companies... Read More →

Tuesday June 28, 2016 1:20pm - 1:50pm
Exhibit Hall B Pennsylvania Convention Center 1101 Arch Street, Philadelphia, PA 19107 USA

2:00pm

#255A: DIA Innovation Theater: Special Session for Exhibitors: Global Trends in Drug Development and Opportunities with DIA Worldwide
Limited Capacity seats available

Component Type: Session
Level: Basic

An exclusive opportunity for DIA Exhibitors! This special session will kick off with a presentation on market insights into global trends in drug development. This informative session will also include an opportunity to meet DIA’s Senior Vice President and Managing Directors from Greater China, Europe, ASEAN, Japan and Americas who will provide upcoming opportunities within their region for 2016 -2017. This is an excellent opportunity to learn about upcoming opportunities where your Company can expand its brand awareness and engage with local stakeholders in your products and services.

AGENDA

2:00 pm Welcome & Opening Remarks
Jonathan Commons
Senior Vice President, Marketing, DIA

2:00 – 2:20pm Global Trends in Drug Development
Michael Kleinrock
Director Research Development
IMS Institute for Healthcare Informatics

2:20 – 2:30pm What’s Happening in China
Carol Zhu
Senior Vice President & Managing Director, DIA Greater China

2:30 – 2:40pm What’s Happening in Japan
Ko Sekiguchi, MBA
Senior Vice President & Managing Director, DIA Japan

2:40 -2:50pm What’s Happening in Europe
Holger Adelmann, MD, PhD
Senior Vice President & Managing Director, DIA EMA

2:50 -3:00pm What’s Happening in Americas
Julie Ho
Associate Director, Business & Market Development, DIA

3:00pm Q/A & Final Remarks
Jonathan Commons
Senior Vice President, Marketing, DIA

Chair

Jonathan Commons

Speaker

Panelist
Michael Kleinrock, MA

Panelist
Carol Zhu, MBA

Panelist
Ko Sekiguchi, MBA

Panelist
Holger G. Adelmann

Panelist
Julie Ho



Chair
avatar for Jonathan Commons

Jonathan Commons

Senior Vice President, Marketing, DIA
Prior to joining DIA, Mr. Commons worked for more than a decade in the Pharmaceutical industry. He most recently served in global roles as the Senior Director of Digital and Patient Engagement at Chimerix and Vice President of Investigator Education and Patient Engagement at Quintiles... Read More →

Speakers
avatar for Holger Adelmann

Holger Adelmann

Senior Vice President and Managing Director, DIA EMEA
Dr. Holger G. Adelmann, MD PhD. Board certified Clinical Pharmacologist. Clinical training in internal medicine. Several leading positions in pharma since 1989 with Bayer & Tropon (Germany), AstraZeneca (UK and Sweden), and Merck Serono (Germany). He is member of the American Association... Read More →
avatar for Julie Ho

Julie Ho

Associate Director, Business and Market Development, DIA
avatar for Michael Kleinrock

Michael Kleinrock

Director, IMS Institute For Health Informatics, Research Development, IMS Health
Michael serves as Research Director for the IMS Institute. He writes and speaks regularly on key  health care topics related to the current and future place of biopharmaceuticals in healthcare.  He brings a deep understanding of complex data sources and analytics from IMS and elsewhere... Read More →
avatar for Ko Sekiguchi

Ko Sekiguchi

Senior Vice President and Managing Director, DIA Japan
avatar for Carol Zhu

Carol Zhu

Senior Vice President and Managing Director, DIA China


Tuesday June 28, 2016 2:00pm - 3:00pm
Exhibit Hall B Pennsylvania Convention Center 1101 Arch Street, Philadelphia, PA 19107 USA

3:25pm

#256: Veeva Innovation Theater: 2016 Paperless TMF Survey: Trends and Insights
Limited Capacity seats available

Component Type: Session
Level: Intermediate

Hear results from the third annual Veeva Paperless TMF Survey, which analyzes the observations of trial master file (TMF) owners from around the globe to identify the barriers, business drivers, and benefits of moving to fully paperless TMFs. Learn how much has changed over the last three years as organizations move along the TMF maturity continuum from passive to active eTMF.

Chair

Veeva Systems


Chair
VS

Veeva Systems, Inc.

NA
Veeva Systems Inc. is a leader in cloud-based software for the global life sciences industry. From compliant promotional content management to best-in-class multichannel marketing, Veeva provides innovative marketing solutions to more than 200 pharmaceutical and biotech companies... Read More →

Tuesday June 28, 2016 3:25pm - 3:55pm
Exhibit Hall B Pennsylvania Convention Center 1101 Arch Street, Philadelphia, PA 19107 USA
 
Wednesday, June 29
 

9:45am

#306: SAS/JMP Innovation Theater: Efficient Safety Assessment in Clinical Trials Using the Computer-Generated Adverse Event Narratives of JMP Clinical
Limited Capacity seats available

Component Type: Session
Level: Intermediate

ICH E3 recommends that sponsors provide written narratives describing serious adverse events or AEs of special interest. Completing narratives offers numerous practical challenges: allocating sufficient resources to meet timelines, reviewing disparate data sources, updating text to reflect changes in study data, and accommodating differences in narrative content according to disease area. We describe how narratives can be generated directly from study data sets and tailored using JMP Clinical.

Chair

SAS Institute Inc. JMP Division


Chair
SI

SAS Institute Inc. JMP Division

JMP, A Business Unit of SAS

Wednesday June 29, 2016 9:45am - 10:15am
Exhibit Hall B Pennsylvania Convention Center 1101 Arch Street, Philadelphia, PA 19107 USA

12:00pm

#330: SAS Innovation Theater: Empowering Action – Fueling Safety and Operational Efficiency
Limited Capacity seats available

Component Type: Session
Level: Intermediate

For groups like Medical Affairs and Clinical Operations, knowing there is a safety or quality issue in a trial is not enough. Value comes from providing capabilities that are approachable and scalable and directly support the ongoing needs to assess, resolve, and learn from a signal. This session will demonstrate an integrated software platform geared toward supporting the ongoing work of clinical professionals while simultaneously creating a rich data asset to improve and enhance delivery.

Chair

SAS Institute Inc.


Chair
SI

SAS Institute Inc.

SAS Institute Inc

Wednesday June 29, 2016 12:00pm - 12:30pm
Exhibit Hall B Pennsylvania Convention Center 1101 Arch Street, Philadelphia, PA 19107 USA

12:40pm

#332A: Salesforce Innovation Theater: Connect to Your Patients, Providers, and Partners in a Whole New Way with the Salesforce Platform
Limited Capacity seats available

Component Type: Session
Level: Intermediate

Life science leaders are shifting towards the patient and using the Salesforce platform to drive this transformation. Hear inspiring stories of how Salesforce’s pharmaceutical, medical device, and CRO customers have connected with patients, providers, and partners to build personalized relationships at scale. See a live demo of Salesforce Health Cloud, the platform delivering a complete view of the patient journey, improving patient acquisition, patient services, therapy adherence, and more.

Chair

Salesforce


Chair
Wednesday June 29, 2016 12:40pm - 1:10pm
Exhibit Hall B Pennsylvania Convention Center 1101 Arch Street, Philadelphia, PA 19107 USA

1:20pm

#332B: SAP Innovation Theater: Too Much R&D Data to Develop New Drugs and Medical Devices?
Limited Capacity seats available

Component Type: Session
Level: Intermediate

Making sense of Big Data in R&D is challenging. Relevant information comes from many sources and in varying formats. Collecting, consolidating and analyzing this data can take long – too long.

This presentation will show how to manage Big Data in R&D efficiently. Find out how to analyze scientific texts, genomics, clinical data and postmarket studies. Hear how to consolidate and analyze structured and unstructured data in real-time. See how visualization can help gain relevant insights.

Chair

SAP America Inc.


Chair
Wednesday June 29, 2016 1:20pm - 1:50pm
Exhibit Hall B Pennsylvania Convention Center 1101 Arch Street, Philadelphia, PA 19107 USA

3:25pm

#355: DBMS Consulting/Clinical Ink Innovation Theater: Safety Data Delay Is a Risk-Enhanced Signal Detection with Customized MedDRA and Drug Grouping Queries
Limited Capacity seats available

Component Type: Session
Level: Intermediate

When it comes to data availability, review time is money. With safety-related data, delays are a risk - not an option. eSource provides real-time clinical data availability, including site-friendly eSAE forms that minimize the site burden and timeline for receipt of critical safety data. Custom Query Tool (CQT) provides Safety Monitors the leverage to bring safe products to market and keep existing products safe as well. Customize MedDRA and WHOdrug queries to discover safety signals and manage risk management.

Chair

DBMS Consulting


Chair
Wednesday June 29, 2016 3:25pm - 3:55pm
Exhibit Hall B Pennsylvania Convention Center 1101 Arch Street, Philadelphia, PA 19107 USA