Business Innovation Opportunities for Nurses

As front-line caregivers, nurses have long operated under a consumer-centric care model—innovating around institutional roadblocks by implementing small-scale changes with potential to solve large-scale problems and improve patient care. Now, business innovators are looking to nurses to be entrepreneurs for them. This study focuses on business innovation opportunities for nurses. Complete this survey on business innovation opportunities for nurses. 

Executive Summary
Sales Enablement in the Healthcare Industry: Understanding the Challenges Facing Marketing and Sales Collaboration Amid a Digital Transformation

This executive summary of a recent industry poll conducted by Seismic, the importance of sales enablement tools becomes clearer, as well as an apparent disconnect between understanding, implementation and measuring success of sales enablement programs within an organization. Learn more.

Exploring Blockchain-Enabled Brand Protection
December 18, 2018 | 11am ET / 8am PT | Systech

Join Joe Lipari, Director of Cloud Products at Systech, and a special guest (soon to be announced), as they explore the path to the future -- from compliance beyond the barcode to the blockchain-enabled pharmaceutical supply chain.

Drug Lifecycle in Our Connected Age: A Shift to Digital R&D and Beyond
December 13, 2018 | 10am ET / 3pm GMT | Accenture

Join this webinar and explore how science and technology advances are providing unprecedented opportunity to change traditional ways of working in the life sciences industry from early drug develop through to commericalization. The healthcare landscape is changing; it’s never been more human. Maximize the value of digitization within your organization.

Right-to-Try or Right-to-Ask? Understanding Right-to-Try and FDA’s Expanded Access
December 11, 2018 | 1pm ET / 10am PT | Rho

This webinar will explore both Right-to-Try legislation and existing Expanded Access Programs, including:

  • Understanding sponsor responsibilities under these programs and when products may be eligible for these program
  • Evaluating options such as treatment protocols, treatment INDs, and emergency use
  • Discussing development risks associated with participation in these programs
Insights for Success with 505(b)(2), the Pathway of Choice
November 28, 2018 | 11am ET / 8am PT | Camargo

This webinar will benefit executives at Biotech and Pharmaceutical companies interested in learning more about 505(b)(2), the pathway of choice. When executed properly, this regulatory pathway enables a lower cost, lower risk, and faster path to approval and market. Register Now!

Content Analytics for the Medical Device Marketer
November 27, 2018 | 2pm ET / 11am PT | Seismic

Tying content to revenue and proving its ROI can be difficult. Join the webinar to learn why understanding content analytics is so important to medical device marketers, what metrics you should be tracking, and how sales enablement can help tie content to revenue. Register now!

Becton Dickinson’s Digital P2P Solution Simplifies Spend Management
Coupa Software

Tina Soliz, Becton Dickinson Requisition to Pay Manager shares how she implemented Coupa for an easy-to-use purchase to pay process that provides transparency into business spend across the organization. Watch this short webinar to gain insight on implementation best practices and lessons learned. 


Evaluation of the claraT Total mRNA report in an RNA- Sequencing dataset from malignant melanoma cancer patients treated with Ipilimumab
Almac Diagnostic Services, part of the Almac Group

claraT is a unique software-driven solution that classifies biologically relevant gene expression signatures into a comprehensive, easy-to-interpret report.  Download the whitepaper.

QSP Approaches to Determine Best in Class Properties for Targeted Anabolic Growth Factor to Arthritic Joints
Applied Biomath

This on-demand webinar introduces a QSP model of targeted anabolic growth factors for intra-articular injection for the treatment of diseased joints that was used to systematically map out drug- and target-parameter space to:

  • Identify tradeoffs between target and drug properties
  • Maximize therapeutic window and tissue targeting
  • Identify key missing data

Watch the webinar today.

Putting the Researcher in the Driver’s Seat
Reprints Desk, Inc.

Historically, researchers have been bogged down by a fragmented assortment of products and services—each addressing a different aspect of the research workflow. Finally, things are starting to change! Read this eBrief to learn how modern tools are speeding scientific discovery. Download now.

Incorporating PROs Into Your Development Program
Recorded on November 16, 2018 | Cardinal Health

Join Cardinal Health experts in the second of our three-part webinar series, as we review the qualitative phase of PRO instrument development within the context of an individual drug development program, PRO instrument modification and regulatory requirements associated with development of these measures for specific populations. Register now!

Challenges And Opportunities In Clinical Data Management
Oracle Health Sciences

A recent research study reveals that more than half of the clinical data professionals surveyed are not confident in the quality and completeness of their clinical data from an audit and compliance perspective.  Download the research report.

Clinical Operations Report: Learn the Top Industrywide Priorities

Results from one of the industry's largest, global clinical operations surveys shares how pharmas and CROs are evolving clinical trial processes.  Download the report.

Modernizing Life Sciences Manufacturing with Machine Learning
Recorded on November 15, 2018 | Amazon Web Services

Modernizing manufacturing equipment, processes, and infrastructure with the newest technology has become a focus to improve their efficiency and overall bottom line. Attend this webinar and learn how to utilize connected IoT devices and data analytics to optimize manufacturing processes, novel ways to use machine learning technology in the cloud, and more.

Migraine Treatment and Calcitonin Gene-Related Peptide Inhibitors: Real-World EHR Case Study

New treatments hold promise of relief to millions of migraine sufferers, but how controlled clinical trial results align with the everyday management of migraine remains unclear. Veradigm researchers used real-world data from a large ambulatory database of de-identified medical records to show how real-world evidence may be leveraged to assess migraine management.

Five Foundational Steps to a Successful RIM Program
November 14, 2018 | 1pm ET / 10am PT | Veeva

Join us to hear Steve Gens, managing partner at Gens and Associates, provide real-world examples for each step and guidance on how to justify making these changes within your organization. This webinar will outline five actionable steps to help you establish roles and responsibilities, institute key processes, and improve long-term outcomes. Register Now!

The Future of Cell & Gene Therapy
Signals Analytics

Cell & gene therapy (CGT) has emerged as one of the most exciting areas of biotechnology. Signals Analytics, with its leading cloud-based data platform, Signals Playbook™, has explored the data to get us closer to understanding the future of CGT.  Download the whitepaper now.

QSP Approaches to Determine Best in Class Properties for Targeted Anabolic Growth Factor to Arthritic Joints
Recorded on November 8, 2018 | Applied Biomath

This webinar introduces a QSP model of targeted anabolic growth factors for intra-articular injection for the treatment of diseased joints that was used to systematically map out drug- and target-parameter space to:

  • Identify tradeoffs between target and drug properties
  • Maximize therapeutic window and tissue targeting
  • Identify key missing data


Using NLP at Novo Nordisk to Generate Actionable Insights from Real World Data
Recorded on November 7, 2018 | Linguamatics

Learn how to use advanced tools and technologies, such as natural language processing, to identify macro and micro healthcare market trends in the US, detect patterns in clinical trial protocol deviations, and discern patterns in patient sentiment, compliance, routines, behaviors, and overall treatment satisfaction and outcomes. 

The Evolving Role of Clinical Data Management
Recorded on November 6, 2018 | Rho

This webinar will examine the effect of technology advancements on the future responsibilities of clinical data managers and discusses the needs introduced by the application of new technologies and broader data source availability.

Capsule-Based DPIs – Understanding the Science
Recorded on November 5, 2018 | Qualicaps

This webinar will discuss several capsule formulations used in DPIs and will compare their performance, an overview on some of the novel methods being employed to evaluate the physical characteristics and mechanical properties of capsules, and the factors influencing the aerosolisation performance of different capsule types. RSVP to watch on-demand!

Choosing the Best Sterile Dosage Form for Your Clinical Supply Needs
Patheon, part of Thermo Fisher Scientific

There are many parenteral dosage forms from which the pharmaceutical scientist can choose to develop their drug product. To make the right choices the pharmaceutical scientist needs to employ a sound development strategy. Download the whitepaper to learn more.

Why Life Sciences Companies Leverage Managed Regulated Infrastructures
Outer Edge Technology

Outer Edge Technology specializes in designing and managing regulated cloud-based infrastructures for the Life Sciences Industry – typically leveraging the AWS and Microsoft Azure platforms.  Once live, we provide the documentation required for the IQ validation process.  Download the article today.

The Use of Electronic Informed Consent in a Blood Collection Study
Recorded on October 31, 2018 | Roche and Medidata Solutions

Clinical research and biobanking industries are rapidly adopting eConsent as an alternative to paper. Learn how eConsent can provide patients with clear and easy-to-understand clinical trial information, improve patient compliance, reduce inspection finding, and enable process efficiencies. Register now!

Navigating Particle Challenges in Sterile Drugs from Component to Patient
Recorded on October 30, 2018 | West Pharmaceutical Services, Inc.

Using a holistic approach to selecting and testing primary packaging and delivery systems can help pharmaceutical manufacturers mitigate particulate risk. Join West experts to learn how a holistic approach to drug product packaging, testing and evaluation can help reduce risk and overcome challenges associated with particulate. Register now!

Scaling Healthcare IT in the Cloud: HIPAA and Other Considerations
October 25, 2018 | 11am ET / 8am PT | Amazon Web Services

Public cloud services adoption is appealing to healthcare organizations striving to provide truly connected health systems with the ability to scale on demand, lower infrastructure costs, and quickly analyze massive data inputs from a variety of sources. Attend this webinar and learn how to simplify your cloud journey, extend your security policies, and automate processes to help meet key healthcare regulations.

Development Advice for Gene Therapy Products
Recorded on October 24, 2018 | Rho

It has been and big year for gene therapy. This webinar will review Commissioner Gottlieb’s statement, provide an overview of the six guidance documents, and discuss the implications for development of new gene therapy products from the perspective of regulatory strategy, clinical development, pharmacology/toxicology considerations, and CMC development.

Are Quality Relationships Possible Without Engagement?
Recorded on October 23, 2018 | Epocrates, an athenahealth service

84% of patients ask healthcare providers about a drug they saw in an ad. This presents a challenge to pharma – how can outreach initiatives optimize engagement? During this webinar, presented by Epocrates, an athenahealth service and DRG Digital, you'll learn about Pharma’s current challenges in maintaining share of voice, today’s goals for using digital channels, and definitions of campaign success. Save your seat now!

Paid Marketplace
[Workshop] Smart Drug Development & Design from Candidate to Phase I

It is important to leverage the skills and experience of experts and connect the dots between competencies to optimize the development pathway and enable drug candidates to reach their true potential. This presentation outlines key considerations for transitioning including API and formulation development, pharmacokinetic and preclinical toxicology studies, and regulatory requirements. Find out more here!

2018 State of Technology in Clinical Research
Forte Research Systems

With this report, discover what over 800 research professionals think about technology's impact on clinical trial operations and learn the necessary steps to see more value from your research systems. Click here to download.

Paid Marketplace
[Infographic] Accelerate Your Early Drug Delivery Journey

To successfully develop increasingly complicated molecules faster, it’s often important to supplement innovator’s expertise with broader experience in formulation and specialized drug delivery technologies. Catalent has the specialized capabilities and experience to supplement your expertise. Find out more by downloading this infographic.

Executive Summary
[Executive Summary] From Candidate to Clinic

It is critical that drug developers execute several elements related to planning, investment, and understanding of the risks, risk tolerance, and pitfalls inherent in the drug development program. To find out what the development program should include, download the executive summary here.

Bringing Real World Evidence into Clinical Research

Life sciences companies are embracing the essential roles that real world data (RWD) and the generation of real world evidence (RWE) play in the development of new treatments for patients.

This whitepaper will explore three areas where RWD and RWE are being applied to improve the design and execution of clinical studies. Download now to learn more.

Value Creation in the Early Phase
Recorded on October 18, 2018 | Catalent

Watch this webinar to hear from industry experts on reliable approaches that have supported hundreds of small and virtual companies help build value to their lead candidates in early phases of development as well as help accelerate the development process to overcome formulation challenges. RSVP here! 

3DP: Manufacturing the Future of Pharma Today
Recorded on October 16, 2018 | Aprecia Pharmaceuticals, LLC

Join this webinar to discover how ZipDose® by Aprecia enables a new world of powerful formulation solutions for NCE product candidates in Phase I or Phase II development and testing. You’ll also review how 3DP can offer formulation advantages such as better molecule protection, adjustable powder layers and flexibility in dose loading for adaptive clinical trials. 

Modernizing Life Science Manufacturing: How Analytics, IoT and the Cloud are Rewriting Drug Production
Amazon Web Services

Manufacturing is one of the most challenging environments in the pharmaceutical industry. This whitepaper discusses how new data acquisition and analytic technologies can boost manufacturing intelligence and agility, how companies like Merck and Moderna optimize manufacturing operations utilizing the cloud, and more. Download it now!

CTTI’s Comprehensive Guide to Mobile Technologies in Clinical Trials
Recorded on October 11 2018 | Amazon Web Services

This action-oriented webinar will describe in detail the information investigators, sponsors, and service providers need to meet technical requirements, support collaborations, and understand each other’s needs and expectations—providing a pathway forward to make the use of mobile technologies in clinical trials a reality. Register now!

Tufts Research: Strategies from Data Management Leaders to Speed Clinical Trials
Recorded on October 4, 2018 | Veeva

Learn how top pharmas and CROs plan to speed database build and data collection, as well as their top challenges and future priorities. This in-depth research from Tufts follows their industry-wide eClinical Landscape Study, examining the major cause of database build delays and their impact on trial cycle times. Register Now

Critical Insights for Oncology Drug Development in Japan and Asia
Recorded on October 2, 2018 | CMIC

Considering oncology drug development and clinical trial for Asia market? Join the experts from CMIC Group, the largest CRO in Japan, to learn the insights on how to start your early oncology drug development and ensure clinical trial success. Register now!

Conquering Compliance: Insights for Commercial Teams in the Medical Device Industry
Recorded on September 27, 2018 | Seismic

What can sales and marketing teams do to address the issue of compliance? Learn why compliance is so important to sales and marketing teams in the medical device industry, how digital transformation and sales enablement can help sales and marketing teams, and more. Register now!

Ex Vivo/In Vivo Platforms for Translational Oncology Research
September 26, 2018 | 11am ET / 8am PT | Champions Oncology

Champions Oncology PDX models are the most highly-characterized, clinically-relevant cohorts of PDX models to optimally predict success and accelerate the drug development process. This webinar will provide an overview of the various unique and advanced translational tools that are offered by Champions oncology in an in vivo and ex vivo setting. 

1 Year Later – Why did Thermo Fisher Scientific acquire Patheon?
Recorded on September 17, 2018 | Patheon

One year ago, Thermo Fisher Scientific completed the acquisition of Patheon, creating the world’s most comprehensive and sophisticated end-to-end CDMO partner. But what does that mean to the industry today? 

[eBook] Healthcare and Life Sciences - Data Value Chain
Amazon Web Services

Download our new eBook to learn how Healthcare and Life Sciences organizations are taking advantage of solutions from AWS and the AWS Partner Network to obtain value from critical data at every stage of the data value chain.

Navigating Patient Reported Outcomes: Foundational Elements and Recent Trends
Recorded on September 13, 2018 | Cardinal Health

Navigating patient-reported outcomes (PROs) such as unobservable symptoms, treatment satisfaction, quality of life, and treatment adherence is a critical component of a patient centric healthcare system. Join our experts in the first of a three-part webinar series on PROs, as they provide insight on the foundational elements of PROs and recent regulatory trends. Register now!

A Lipid Nanoparticle Quantitative Systems Pharmacology Case Study
Recorded on September 12, 2018 | Applied Biomath

This webinar will present a quantitative systems pharmacology case study which assesses a Lipid Nanoparticle to treat Crigler-Najjar Syndrome Type 1. Learn how the model was used to support translation from preclinical to clinical trials as well as first-in-human dosing.

2018 Weekly Compendium
Biotech Primer

The Biopharma industry is moving at lightning speed and it can be a challenge to keep pace. Here at Biotech Primer we spend hours each week researching, writing, and editing original content for the Biotech Primer WEEKLY with one goal in mind: to help everyone better understand the latest science and technology driving today’s healthcare industry.

This eBook is a collection of Biotech Primer WEEKLYs from the past 12 months. The Biotech Primer WEEKLY is a one-page, easy-to-ready newsletter delivered each Thursday right to your inbox. If you are not already registered to receive the Biotech Primer WEEKLY register today here.

Download here: 2018 Biotech Primer WEEKLY Compendium

Real-World Evidence in the Cloud: How Technology is Revealing the Big Picture in Pharma
Amazon Web Services

Life science companies are responding with Real World Evidence (RWE) programs to capture data from clinical through post-market activities from a variety of sources. Learn how the centralization of data assets enables organizational intelligence by equipping companies to understand the needs of patients and other stakeholders, and how their products can meet them.  Download this Whitepaper!

Understanding New Drug Applications (NDAs)
Recorded on August 14, 2018 | Rho

This webinar will help you understand what is involved in an NDA including regulatory strategy, data integration and readiness, and electronic publishing, and provide tips that can help you avoid common pitfalls in the submissions process.

Executive Summary
Executive Summary: Investigator Site Payments Strategy Survey

As the number of clinical trials increases so does the complexity and number of US and global sites needed to foster trial success. Read what was discovered after a survey on current site payment practices, how these practices are measured, what process improvement initiatives are currently being explored, what are some of the barriers to change, and what site payment trends will occur over the next five years. Download it now!

Paid Marketplace

Develop a basic understanding of principles and concepts of bioavailability of oral drugs. This course, designed for scientists involved in pharmaceutical drug development, will simplify the concepts of bioavailability and how to manage biopharmaceutical challenges, and identify why it is an important factor in optimal therapies for patients. Enroll Now!

The State of Sales Enablement in the Healthcare Industry

Take this quick 10 minute survey on on the state of sales enablement in the healthcare industry. A $5 Amazon Gift Card will be sent to the first 50 qualified respondents. Complete the survey now!

New Findings from the Veeva 2018 Unified Clinical Operations Survey
July 25, 2018 | 12pm ET / 9am PT | Veeva

Hear new results from one of the industry's largest, global clinical operations surveys, the Veeva 2018 Unified Clinical Operations Survey. The Veeva 2018 Unified Clinical Operations Survey examines the industry’s progress toward a unified clinical operating environment.

Industry Report: Findings from the 2018 Unified Clinical Operations Survey

Learn why unifying clinical applications is an industrywide priority for clinical operations leaders. Read the report.

The Changing Landscape of Real-World Evidence and its Impact on Clinical Research
Thursday, June 21, 2018 | 11am ET / 8am PT | TriNetX

Researchers are encumbered with a plethora of disparate data and analytic tools. These assets pose several challenges which need to be overcome to ensure they satisfy their intended purpose. 

Join this webinar to learn how real-time, self-service access to longitudinal patient data is changing the way researchers evaluate treatment effectiveness, safety, protocol design, and more. Register now.

Handling Suspected Fraud and Data Fabrication in Clinical Studies
June 13, 2018 | 1pm ET / 10am PT | Rho

Fraud and fabrication is no laughing matter in the realm of clinical trials.

This webinar will outline the ways in which sponsors and CROs can remain diligent by being aware of signs of possible fraud and fabricated data throughout the course of the study.

Implementing a Proactive Approach to Risk Management

A solid RBM plan will not only help you comply with the ICH guidelines, but will help you mitigate risks which could ultimately delay your trials and increase costs. Download today!

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Your oncology trial is complex. Get specialized expertise, end to end.
Precision for Medicine, Oncology and Rare Disease

The first precision medicine CRO designed specifically for oncology and rare disease, Precision unifies translational science expertise and unparalleled clinical operations to create a more efficient process, deeper data, and an accelerated development pathway for novel treatments.


With 1200+ experts worldwide, one core team delivers


  • Clinical development planning
  • Expedited study start up enabled by Precision’s Oncology Site Network
  • Personalized clinical trial execution services
  • Specialty labs services and coordination
  • Robust biometrics teams and services


Schedule a meeting with our experts at ASCO, Booth 24146, and visit our website