Archives

Webinar
Managing the Risks of Implementing E6R2
Recorded on: March 25, 2020 | Rho

Successful implementation of RBQM is a challenge many in our industry are facing. To understand what it is and how it impacts the management of your clinical trial, this webinar will address what exactly E6R2 is. We will use Rho as a case study for designing and implementing a strategy, discuss common misconceptions, and review lessons Rho has learned through implementation of RBQM. Click here to register for this webinar today!

Webinar
Accelerate Clinical Operations Across Sponsors, CROs and Partners With a Best-of-Breed Partner Like Box
Aired on: March 24, 2020 | Box

Learn how Box is a critical force multiplier in the Best-of-Breed application stack with partners like Nintex, DocuSign and Slack in supporting clinical operations for both regulated and non-regulated content. Register now.

Webinar
Thermo Fisher Scientific Invests $800 Million to Help Biopharma and Pharma Companies Accelerate Commercialization and Bring Medicines to Patients Faster
Recorded on March 23, 2020 | Patheon

Join Thermo Fisher Scientific for a live webcast on its $800 million investments in its biologics, cell and gene therapy, and drug product capabilities to help biopharma and pharma companies of all sizes accelerate commercialization and bring medicines to patients faster.

Webinar
Use Serialization Data to Maximize Performance and Minimize Risks
March 18, 2020 11 a.m. EST / 9 a.m. PST | Systech

Serialized products generate a wealth of data as they move through the supply chain. What if you could access and analyze this data to gain operational visibility and powerful business insight? It’s time to put your serialization investment to work for you. Learn how in this webinar.

Webinar
Translational Modeling Strategies to Predict Clinical Doses for CD3 Bispecific Molecules
Recorded on: March 12, 2020 | Applied BioMath

Learn how a Quantitative Systems Pharmacology (QSP) model and translational framework described for CD3 bi-specific molecules provides a holistic solution for quantitative decision making throughout the drug discovery and development process. Register now.

Webinar
Accelerating Approval for Cell and Gene Therapies
Recorded on: February 27, 2020 | Cardinal Health

Developers of cell and gene therapies can run into complex clinical and regulatory hurdles when bringing treatments to patients. Join experts from Cardinal Health Regulatory Sciences to explore critical factors that can help reduce the risk of failure and increase speed to market. Register for this webinar today!

Webinar
Tufts-eClinical Solutions Data & Analytics Survey Results
Recorded on: February 26, 2020 | eClinical Solutions

Key findings from the 2019 Life Sciences Data & Analytics Survey conducted by the Tufts Center for the Study of Drug Development will be unveiled during this live webinar led by industry expert and study lead, Ken Getz, Director of Sponsored Programs and Associate Professor. Watch On Demand Now!

Webinar
Understanding the New MDR Article 117 and its Impact on Combination Product Applicants and Medical Device Constituent Part Supplier
Recorded on: February 13, 2020 | West Pharmaceutical Services, Inc.

Understanding the medical device design and how it forms integral and non-integral drug device combinations (DDC’s)  is critical to navigate the new European regulatory landscape.Examples of these expectations will be presented to outline the overall impact of Article 117 and additional elements of the MDR 2017/745 pertaining to combination drug products as regulated within the European community.  Register now.

Webinar
InCrowd’s 2020 Healthcare Predictions
Recorded on: February 11, 2020 | InCrowd

How will 2020 change US healthcare? InCrowd’s physicians weigh in on what the new year will bring. Join Diane Hayes, PhD, InCrowd Co-Founder and Board Member and Daniel S. Fitzgerald, InCrowd CEO and President, for InCrowd’s 2020 Healthcare Predictions Webinar. Register Now!

Webinar
Model-Based Approach to Design Bi-Specific Modalities in Early Discovery
Recorded on February 4, 2020 | Applied BioMath

Learn how we used a tiered model-based approach of a bi-specific antibody to appropriately cover multiple antigen pairs to help teams with informed antibody design, prioritization of experiments, and triaging of challenging antigen pairs.  Register today.

Webinar
5 Ways to Make Monitoring More Efficient
Recorded on January 30, 2020 | Veeva

This new year, take a fresh look at your monitoring processes and learn how to improve efficiency across the entire monitoring lifecycle. Register for the webinar here.

Webinar
Cartridge Based Drug Delivery…Evolving Technologies Designed With the Patient in Mind.
Recorded on January 28, 2020 | West Pharmaceutical Services, Inc.

The focus of this webinar will be on the design and process approach for next generation large volume delivery systems for prefilled cartridge delivery, as well as on providing an overview of key critical product requirements, such as compatibility with sensitive drug products, system functionality, and fill-finish implementation. Register now.

Webinar
Perceptions, Myths & New Thinking on Direct-to-Patient Clinical Supply
Recorded on January 23, 2020 | Catalent

This webinar reveals results from a recent industry survey that sought to gain insight on trial sponsors’ perspective on offering a DTP option and their current level of awareness and understanding of any factors that may influence their ability to do so. Register now to learn more.

Webinar
The Art of Recognizing Clinical Supply Risk Factors and Applying Proactive Measures Avoid Study Delays and Disruptions
Recorded on January 14, 2020 | Catalent

Are there certain types of clinical sponsors and studies that are at greater risk of experiencing supply challenges? This webinar will explore aspects of the study protocol that can directly influence clinical supply strategy and how sponsors can proactively understand and address clinical supply-related risks. Register now.

Webinar
Transportation Solutions for Cell & Gene Therapy Supply Chains
Recorded on December 17, 2019 | Thermo Fisher Scientific

From the basics such as service level expectations for couriers versus integrators, to how to evaluate domestic and international lanes, and finally – how to balance risk and cost, this webinar will help you understand how to start tackling your clinical supply chain. Register now.

Webinar
Planning a Rapid Commercial Market Launch for Your Biologic
Recorded on December 4, 2019 | Catalent

In this webinar, AstraZeneca and Catalent Biologics experts will share a case study on a 30-day commercial launch plan for a product into new markets and why this approach was important for patients. Register now.

Webinar
How ICON, Lotus, and Bioforum are Improving Study Efficiency with a Modern EDC
Recorded on December 3, 2019 | Veeva

Hear how ICON, Lotus Clinical Research, and Bioforum are speeding database builds and automating reporting tasks for data management.  Learn how to reap the rewards of a straightforward build and a modern EDC during this webinar. Register now.

Webinar
Striving for Zero in Quality & Manufacturing
November 19, 2019 | 11am ET / 8am PT | OpenText

Pharmaceutical and medical device manufacturers strive towards a culture of zero – zero hazards, zero defects, and zero waste. At the same time, they must meet GxP requirements, update antiquated systems and processes, and address the demands of an increasingly tech savvy workforce. Register now to learn more about the role that content management plays in pharmaceutical manufacturing.

Webinar
Lipid-based Formulations for Early Stage Clinical Trials
Lonza

Liquid-filled capsule technology has a proven record for addressing complex API formulation challenges, but also offers a simple and effective pathway to the clinic. Register now to learn more about lipid-based formulations.

Webinar
OTC Innovation to Avoid Stagnation: Survey Insights, Expert Advice, and Latest Technologies to Boost Your Product’s Performance
November 13, 2019 | 11am ET / 8am PT | Catalent

Join industry experts as they analyze the critical role of innovation in OTC products, and strategies for achieving it. Register now to learn more about survey insights, market trends, and latest technologies.

Webinar
The Promise of Connected Packaging—from Brand Protection to Consumer Insight
Recorded on November 12, 2019 | Systech

The transformations now taking place in the emerging field of connected packaging have the potential to address all these product challenges—protection, engagement, traceability—while delivering powerful supply chain insight. Register now to learn more.

Webinar
Navigating HUB Design in 2020: Insource vs. Outsource vs. Hybrid
November 7, 2019 | 11am ET / 8am PT | Archbow Consulting

Designed for pharma and biotech patient support, brand, and market access teams, this webinar will explore a variety of factors to consider when choosing between insourced, outsourced, and hybrid HUB models. Register now.

Webinar
Improving Diversity in Clinical Research
Recorded on November 6, 2019 | Rho

Why is diversity in clinical trials important? Minority populations are more likely to be diagnosed with certain cancers, stroke, diabetes, and are more likely to die prematurely than White Americans. Health disparities by race and ethnicity could increase if minority populations are not included in clinical trials.

Register now to learn who is participating in clinical trials and why.

Webinar
Unleash the Power of an Integrated Imaging and EDC Platform
November 5, 2019 | 11am ET / 8am PT | Medidata

Integrated Imaging and EDC ensures the right data is presented to the right users at the right time, free from manual intervention. Taking data reconciliation to a whole new level means your trial not only saves time, resources and cost, but also drastically reduces your clinical trial risk. Register now to learn more.

Webinar
Utilizing a Technology-first Approach to Maximize Brand Value & Gain Competitive Advantage
Recorded on October 29, 2019 | SHYFT

In this webinar, we'll highlight some of these approaches and demonstrate how data and analytics can be used to gain a competitive advantage and create differentiation. Register now.

Webinar
Enabling Formulations by Spray Drying: From Early Development to Commercialization
Recorded on October 24, 2019 | Patheon

Discover an approach to solubility and bioavailability enhancement of poorly water soluble drug molecules, approaches to aqueous-based spray drying of bio-pharmaceuticals as well as small molecules intended for inhalation delivery. Join us for this webinar to learn more.

Webinar
Unlock Industry Perspectives on the Advantages and Challenges of Developing Advanced Dosage Forms
Recorded on October 22, 2019 | Catalent

Register for this webinar to learn about the tools and technologies for creating dosage forms such as orally disintegrating tablets (ODTs), multi-particulates, and modified release formulations.

Webinar
Unlock Industry Perspectives on the Advantages and Challenges of Developing Advanced Dosage Forms
October 22, 2019 | 11am ET / 8am PT | Catalent

Register for this webinar to learn about the tools and technologies for creating dosage forms such as orally disintegrating tablets (ODTs), multi-particulates, and modified release formulations.

Webinar
Exploring What Physicians Know and Don’t Know About Nucleic Acid-Based Medicines
Recorded on October 16, 2019 | InCrowd

Dr. Melissa Moore, global messenger RNA (mRNA) expert and chief scientific officer of Moderna’s mRNA research platform, joins Dr. Diane Hayes, InCrowd co-founder and board member, for a webinar exploring the emerging therapy area, medications in the field, and analysis of recent InCrowd prescriber research. Register now to save your seat.

Webinar
Driving Patient Innovation Through Software as a Medical Device
Recorded on November 21, 2019 | Accenture

Accenture experts will explore the emergence of SaMD as a new class of medical device and discuss the potential challenges that biopharma companies face in the development of these solutions. Register for this webinar now.

Webinar
CIOs’ Perspectives: Driving Clinical Trial Innovation with a Unified Platform
Recorded on October 15, 2019 | Medidata

In this webinar, you will hear from Alan Louie, Ph.D, Research Director at IDC, Bill Swavely, CIO at Pharm-Olam, and Rama Kondru, Ph.D, CIO at Medidata about the need for a platform approach in clinical research, the rationale for switching from disparate systems to a unified platform, and the benefits that could be realized. Register now.

Webinar
The Promise of Real-World Data: Using Technology to Enable the Standardization, Transparency, & Replicability of RWD Research
Recorded on October 10, 2019 | SHYFT Analytics

This webinar will address how the use of technology for deploying data and analytic standards can be utilized to meet the challenge of understanding and comparing findings between studies conducted by different researchers, by facilitating the standardization, transparency, reproducibility, and replicability of RWD research. Register now.

Webinar
The Value of Real World Data in Orphan and 505(b)(2) Drug Development
Recorded on October 9, 2019 | Camargo

In this webinar, we'll share insights to harness the strategic value of real world data to build optimized drug development programs that minimize the time and cost of sponsor-driven studies. Register now!

Webinar
Biosimilars and Drug Pricing
Recorded on October 3, 2019 | Elsevier

Join us for this webinar as we bring together a panel of industry experts to discuss the changing landscape of biosimilar development and how it will affect pricing in the future.

Webinar
Synthetic Controls: Best Practices and Regulatory Perspectives
Recorded on October 2, 2019 | Medidata

With increasing competition for patients, the ability to effectively and efficiently execute on clinical development plans has increased focus on alternative data sources. In this one-hour session attendees will hear from former FDA leaders and industry experts who will address what Synthetic Control is and how it can be leveraged in clinical development.

Webinar
Process Characterization: Ready For the FDA?
Recorded on October 1, 2019 | Thermo Fisher

Eight years after the FDA issued its guidance of process validation, some still ask the question “Is process characterization optional anymore?” This webinar will cover the basics of process characterization, whether it is optional or not, and what “good” process characterization really looks like. Register now!

Webinar
Effective Combination Products Risk Management Programs: Special Considerations for Control and Analytical Testing Strategies
Recorded on September 26, 2019 | West Pharma

Developing a combination product? Join experts Susan Neadle, Sr. Director, Global Value Chain Quality Design, Johnson & Johnson and Jennifer Riter, Sr. Director, Lab Services, West to learn how you can create an effective risk management program. Register Now!

Webinar
Building the Digital Biotech Company
Recorded on September 25, 2019 | AWS and Moderna

Hear from Moderna’s Chief Digital and Operational Excellence Officer how they have eliminated data siloes to accelerate data-driven decisions at an enterprise level, and established a production environment capable of consistent delivery of complex drug products including a “batch of one”. Register Now!

Webinar
De-Risking the Solid Form Landscape of an API
Recorded on September 19, 2019 | Cambrex

This presentation will discuss how predictable stability and solubility can minimize development timelines and cost. Attend to hear about two case studies exemplifying the importance of understanding the hydration space of an API and how hydrate formation may be avoided by development of a robust crystallization procedure.

Webinar
Overcoming Challenges of Bioanalytical Method Development for Oligonucleotides and Large Molecules
Recorded on September 18, 2019 | CMIC

Please join the experts from CMIC Group, Japan’s largest CRO with over 30 years of analytical service experiences in US and Japan, to learn the insights and tips on developing an immunogenicity assay in a regulated laboratory, selecting a format for the neutralization assay for immunogenicity assessments, and quantitative Bioanalysis of Oligonucleotides by LC-MS. Register Now!

Webinar
Flexible Manufacturing Strategies: What’s Best for Your Product?
Recorded on September 17, 2019 | Catalent

In this webinar, manufacturing experts will discuss the benefits of end-to-end solutions and share case studies on how flexible manufacturing strategies can accommodate the changing landscape of pharmaceutical products and help bring a drug to market. Register now!

Webinar
Challenges with Fast Enrolling Post-Operative Acute Pain Studies
Recorded on September 11, 2019 | Rho

Enrollment can be very fast for post-operative acute pain studies which brings with it unique challenges in study execution. This webinar will address the differences between bunionectomy and abdominoplasty models, the importance of rater and site training, and considerations for data collection and analysis.

Webinar
Achieve Better Patient Outcomes with Clinically Supported, Tech-Enabled Adherence Programs
Recorded on August 29, 2019 | Lash Group

Join Lash Group’s Vice President of Market Development and Strategy, Michael Craig, and Product Director of Adherence Services, Dale Hanna, as they discuss the critical nature of clinical expertise in tech-enabled patient support solutions and the importance of training teams in empathy. Register now.

Webinar
A Paradigm Shift to Realize Intelligent Clinical Trial Oversight
Recorded on August 8, 2019 | Medidata

Nick Dyer ( CEO, Catalyst Clinical Research ) and Stacey Yount ( VP of Product, Trial Management Solutions, Medidata ) will discuss the industry challenges and share how Medidata’s Rave CTMS breaks down operational silos by providing a centralised solution to manage issues, deviations and associated actions. Register now.

Webinar
Three Ways to Save Time and Execute a Successful RIM Implementation
Recorded on July 30, 2019 | Veeva

Join this webinar to hear from two of Veeva’s subject matter experts, Lalana Dararutana and Serena Peirson, on ways to achieve a successful RIM implementation. Register Now!

Webinar
End-to-End Analytical Technology for Process and Quality Improvements in Biologic Drug Production
Recorded on July 25, 2019 | Thermo Fisher Scientific

Join this webinar to learn how Raman, NIR, and mass spectrometry provide raw material ID and bioprocess monitoring for:

  • cell culture and fermentation monitoring
  • moisture analysis of lyophilized materials
  • near real-time discrimination of bulk protein product

Register Now!

Webinar
Accelerate Your Life Sciences Business Through a Modernized and Compliant Process
July 24, 2019 | 2pm ET / 11am PT | DocuSign

Join this webinar to learn how industry leaders are using DocuSign to modernize their systems of agreement while implementing GxP validation processes. Hear best practices about how to simplify and scale your business processes while also reducing your regulatory risk.

Webinar
Accelerating Site and Patient Enrollment for Phase 1 Trials
Recorded on July 23, 2019 | Medrio

This Fierce webinar will feature clinical trial site leaders and R&D executives, who will pass along the latest strategies for boosting site and patient enrollment in phase 1 trials. They will discuss best practices for communicating with both investigators and patients. Register now to learn more.

Webinar
The 505(b)(2) Pathway: Getting to the Clinic Faster
Recorded on July 16, 2019 | Camargo

You’ve identified your product as a candidate for approval via the 505(b)(2) pathway and completed a successful pre-IND meeting. What comes next? Register now to find out!

Webinar
The Missing Link in Marketing: HCP Impact
June 26, 2019 | 2pm ET / 11am PT | 81qd

Understanding the existing relationships among health care professionals not only optimizes your ability to connect with them, but it also maximizes the impact of marketing communications in achieving the desired clinical behavior change that will improve patient care.

Join our webinar to learn more about how you can do more with less through “HCP Impact” strategies.