Webinar
ctDNA Applications for Breast Cancer Trial Design
Tuesday, October 27, 2020 | 4pm ET / 1pm PT | Natera

Discover the latest advantages of using a personalized, tumor-informed circulating tumor DNA (ctDNA) test to design oncology clinical trials in solid tumors, and Breast Cancer in particular.  Learn how Signatera, a breakthrough technology, can be applied in early stage and late stage cancer trials, potentially enriching for patients most likely to respond to therapy, accelerating time to trial readout, or identifying early relapsers. Register Now

Webinar
Building a Flexible, Challenge Resistant and Patient Centric Clinical Supply Chain
October 27, 2020 | 11am ET / 8am PT | Catalent

In this webinar, learn the benefits of utilizing demand-led supply and direct-to-patient distribution models in the clinical supply chain, as well as how they can be used to both improve flexibility and better align with patient needs. Register now. 

Webinar
Highly Potent Strategies from Early Development to Commercialization
November 4, 2020 | 11am ET / 8am PT | Thermo Fisher Scientific

Pharmaceutical R&D is focusing on developing ever more specialized drugs, resulting in increasingly more potent APIs. Therefore, the demand for highly potency drug product manufacturing has been steadily increasing over the years and this trend is expected to continue. Is your highly potent strategy efficient and optimal to scale-up? Register now.

Webinar
How technologies are transforming high volume injections - essential enablers for patient outcomes
November 5, 2020 | 11 a.m. EST / 7 a.m. PST | West Pharmaceutical Services

This webinar will explore why adherence, safety and quality of life are important for patients, and how these key enablers contribute towards positive outcomes. We will also discuss existing challenges, such as drug development, regulatory, patient accessibility, and how device technologies can further improve patient outcomes. Register now.

Webinar
Elevate Your Digital Events Strategy
Veeva

Looking for ways to engage with HCPs more effectively in your virtual events? Join this 45-minute webinar including a live Q&A, on Tuesday, November 10, and learn how to optimize customer engagement across channels. Register Now.

Webinar
Cell and Gene Therapy - CMC Challenges and Strategies
Wednesday, November 11, 2020 | 1pm ET / 10am PT | Cardinal Health

In this webinar, experts from Cardinal Health Regulatory Sciences discuss CMC challenges and potential mitigation strategies illustrated through multiple case studies. Cell and gene therapy developers, research scientists, regulatory and legal professionals are all encouraged to attend. Register Now!

Webinar
Cut Time, Not Corners: Smart Processes to Include in Your Phase 1 Clinical Development Program to Save Time & Cost Yet Add Value to Your Clinical Asset
Thursday, November 12, 2020 | 12pm ET / 9am PT | Frontage Laboratories

Phase 1 clinical program planning is complicated these days with added pressure to get maximum study data and move quickly to Phase 2 or partner the clinical asset. During this webinar, presenters will review specific study components which can be highly beneficial in terms of time and cost savings when included in a Phase 1/ First-in-Man clinical studies. Register now for an insightful overview for anyone new to Phase 1 clinical study operations and useful information for those who have not run an early clinical program in some time.

Webinar
Best Practices for Implementing and Maintaining Successful Standards
November 17, 2020 | 11am ET / 8am PT | 4G Clinical and Veeva

Few organizations maintain standards successfully over time. Join this webinar to develop best practices and checklists that can be applied across any size organization, regardless of standard type, to ensure efficient clinical trials. Register now.

Webinar
Hindsight is so 2020 - Getting Ahead of CNS Trial Enrollment in a Rapidly Changing Clinical Landscape
November 18, 2020 | 1pm ET / 10am PT | Rho

The past six months have highlighted both existing and unexpected enrollment challenges, as sponsors, CROs, and sites have been pressed to evolve their recruitment strategies. Join us as Rho experts discuss their approach to adapting CNS trial enrollment to a rapidly changing clinical landscape. Register now.

Webinar
Saving Development Time with Single Vendor Approach
November 20, 2020 | 11am ET / 8am PT | Thermo Fisher Scientific

Watch this webinar to learn how using a single vendor will save you time and money. The presentation will focus on the Integrated Offering and how it is defined for the client, with the focus on simplicity, time savings, reduced risk, and proven experience. Register now.

Archives

Webinar
Streamline Your Clinical Research Organization's Processes End to End, Featuring IQVIA and Syntactx
Recorded on October 22, 2020 | Salesforce and FinancialForce

Learn why consolidating Discovery, Pre-Clinical, Clinical, and Post Approval processes on a single platform drives efficiencies, margin improvement, and real time collaboration internally & externally. Register now!

Webinar
Gene therapy viruses’ production and quality control
Recorded on Thursday, October 22, 2020 | Frontage Labs

Gene therapy has become a one-time treatment method for a complete cure by fixing genomic errors which altered protein functions of normal cells. The high titer virus packaging and purity are essential for the success of clinical gene therapy. In this presentation, we report to establish a facility to manufacture GLP grade viruses and to develop the relevant QC assays at Frontage. Our efforts will facilitate the application of this modern cutting edge technology in clinical arena. Register Now

Webinar
Leveraging a "Reverse Engineering Methodology" in Drug Development for On-time Delivery during COVID-19
Recorded on Wednesday, October 21, 2020 | Cambrex

Join us for a live webcast that will showcase valuable case studies and new methodologies that can help the wider CDMO industry in tackling delays in project deliveries. We will also cover our strategy to ensure the delivery of drugs to customers and patients in spite of the COVID-19 outbreak. Register now.

Webinar
Pathways to Value: Biopharma's Options for Global Expansion
Recorded on October 20, 2020 | Blue Matter Consulting

US biopharma companies have options for ex-US expansion. But how can a company decide on its best pathway to value? In this webinar, leaders who’ve done it outline how they weighed their options and made the right decisions.

Webinar
The Faster Path to Self-Administration: Moving from Pre-Filled Syringe to Auto-Injector
Recorded on October 15, 2020 | Catalent

In this webinar, Catalent Biologics shares how to transition your product from pre-filled syringe to auto-injector more quickly with an experienced partner who can anticipate equipment and process needs. Register now.

Webinar
How to Deliver a Seamless Virtual Selling Experience
Recorded on October 14, 2020 | Salesforce

Join this webinar to learn how to more efficiently engage with customers remotely using your digital footprint, how to maximize product launches virtually, and how to proactively identify customer support needs by leveraging analytics and insights. Register now!

Webinar
Lifecycle Management Strategies Targeted For Patient Populations with Swallowing Disorders
November 5, 2020 | 11 a.m. EST / 8 a.m PST | Adare Pharma Solutions

This webinar will discuss life cycle management strategies for patients with swallowing disorders and the overall impact on patient perception. The webinar will include several panel speakers representing different perspectives and case study examples. Register now.

Webinar
Digitize remote site monitoring with Box
Recorded on Tuesday, October 13, 2020 | 2pm ET / 11am PT | Box

Accelerate R&D processes across the value chain, maintain GxP compliance and reduce your overall IT footprint. Access, collaborate, and exchange non regulated and regulated content from one repository with Box. Register Now

Webinar
IVDR – A Game Changer for Companion Diagnostics in Europe
Recorded on: October 8, 2020 | Qiagen

The testing landscape for companion diagnostics (CDx) in Europe will change. Register now and learn how to ensure patient access to IVDR-compliant CDx in Europe. 
 

Webinar
Mitigating Covid-19 through a hybrid decentralized clinical trials approach
October 7, 2020 | 1pm ET / 10am PT | Rho

COVID-19 has presented the industry with many risks and challenges to the management of clinical trials. For many, the mitigation of these issues has accelerated the implementation of decentralized approaches to trials. Join us as we discuss these issues, ways they can be addressed, and Rho as a case study. Register now. 

Webinar
From Concept to Market: Overcoming the Challenges of Manufacturing and Clinical Trials
Recorded on Tuesday, October 6, 2020 | Alta Sciences

In this webinar, we will reveal the inner workings of the manufacturing and pharmacy department of a CRO/CDMO, so you understand the different regulatory and operational considerations faced by a clinical research pharmacy. You will learn about inherent challenges, and the appropriate mitigation measures and optimization solutions that deliver the most effective results and outcomes. Register Now.

Webinar
Phase Appropriate Expertise and Technologies to Accelerate Product Development to Commercialization
On-Demand | Catalent

In this webinar, pharmaceutical scientists present real-life examples of challenges they’ve overcome in the transfer of oral small molecules from a dedicated early-phase development site to a dedicated late-phase manufacturing site. The experts share collaborative best practices and explain how features of Catalent’s OneXpress™ can reduce risks, accelerate timelines, and maximize utilization of resources across a global network to drive more successful outcomes. Watch now.

Webinar
West addresses challenges for oncology drug development & delivery
Recorded on: September 30, 2020 | West Pharmaceutical Services, Inc.

This webinar will place the oncology patient and the drug company at the heart of the conversation and will give situational awareness of the challenges both parties face, along with the proven solutions to help overcome these challenges. Register now.

Webinar
Conventional vs. Unconventional Spray Drying Strategies: Development to Commercialization
Recorded on September 30, 2020 | Thermo Fisher Scientific

Leverage spray drying to combat bioavailability and processing challenges. Learn more as global industry experts provide insight from early development to commercialization. Register now.

Webinar
De-risk Antibody and CAR-T Safety by Identifying Off-target Specificity
Recorded on Tuesday, September 29, 2020 | Integral Molecular Inc

This webinar assembles experts with experience in biotech, pharma, and the FDA to discuss how to best identify the off-target liabilities of antibody and CAR-T therapies that are the primary cause of failure in preclinical and early clinical studies. Register Now

Webinar
Using Big Data to Take Quality Beyond Compliance
Recorded on: September 24, 2020 | MasterControl

In this webinar, learn how an advanced quality management system (QMS) that connects data across the product life cycle can provide business intelligence insights and give management a better understanding of your processes and how to improve them. Register now.

Webinar
New vaccines? How to go from zero to serialized in six months.
Recorded on: September 23, 2020 | Systech

Whether you’re developing a COVID-19 treatment or introducing a new drug to the market, serialization is a requirement. Learn why a configurable solution will get you to compliance faster, future-proof your deployments and reduce total cost of ownership. Register now.

Webinar
Technology Transfers: Best Practices for Optimizing Success and Mitigating Risk
Recorded on September 22, 2020 | Thermo Fisher Scientific

Learn how technology transfers can optimize success and mitigate risk from product development to commercial launch. Register now!

Webinar
ESMO Postview: Highlights from the virtual conference
Recorded on: September 22, 2020 | Fierce Biotech

Cancer experts and pharma execs will break down the headline-making data from ESMO, sharing their insights and analysis around the conference’s most closely watched studies. This discussion will examine how groundbreaking research unveiled over the weekend will change clinical practice and prime drugs for key new indications, and panelists will fill you in on the need-to-know takeaways from oncology’s hottest fields. Register now.

Webinar
USP Elastomer Chapter Revisions Will Become Official December 2020: What you Need to Know
Recorded on: September 17, 2020 | West Pharmaceutical Services, Inc.

This webinar will explain the baseline requirements for elastomeric physicochemical and functional properties.  Examples to illustrate qualification of components for intended applications will be included.  Register now.

Webinar
Wearable Technology for High-Frequency Cognitive and Mood Assessments in Depression
Recorded on September 17, 2020 | Cambridge Cognition

The widespread adoption of smartphones and wearables makes monitoring symptoms in real time a credible option using brief measures designed for these devices – but is this acceptable and feasible for patients? This webinar will delve into the research findings of Takeda Pharmaceuticals, Cambridge Cognition, and CTRL Group, and share lessons learned adopting new technologies in clinical trials. Register now.

Webinar
Increasing Patient Adherence for Isolated Populations During the Pandemic: Formulation Strategies Focused on Patient Centric Solutions
Recorded on: September 16, 2020 | Adare Pharmaceuticals

This webinar will focus on the challenges isolated populations have faced during the global pandemic related to patient adherence, and the application of formulation strategies to create more patient centric solutions. Register now.

Webinar
Overcoming Scalability Challenges with Autologous Therapies
Recorded on: September 15, 2020 | Catalent

Join experts Prof. Gerhard Bauer and Catalent’s Dr. James Crutchley as they discuss challenges and an innovative methodology to commercially scale autologous therapies. Register now.

Webinar
Accelerating Pharma’s Evolution Towards a Perfect Omnichannel Engagement
Recorded on September 15, 2020 | CSL Behring & Abbott

Do you want to better engage with your customers in the new normal? Do you want to know about the secret sauce to perfecting omni-channel marketing? Join the experts to review the current strategies and discuss the key enablers to driving a personalized customer experience. Register now.

Webinar
Improving Patient Outcomes & Clinical Trials With Visual Analytics
Recorded on September 10, 2020 | Tableau

Drug Development has always been about data.  Research insight that comes from data often gets muddied by its vastness and inaccessibility. In this session we discuss Takeda Pharmaceutical’s Platypus, a comprehensive set of Tableau visualizations of clinical trial data. With the power of Tableau, Takeda is able to more effectively monitor patient safety through all clinical trial phases and help ensure data quality, leading to timely analysis and ultimately a faster path to life-changing medicines that patients need. This session will explore: how to increase quality and speed in data analysis to reduce time and achieve greater results, the impact of Takeda’s approach and user testimonials, and data visualizations, such as “COVID19 Patient Visit Dashboards,” show pandemic insights and enable study teams to view patient data, behavior patterns, and trial delivery milestones. Register Now

Webinar
Leveraging Innovative Technologies, Best Practices and Strategies to Accelerate Biologics Development and Commercialization
Recorded on September 9, 2020 | Thermo Fisher Scientific

This webinar will detail practical implementation of innovative technologies and solutions such as multi-attribute method, modernized cell line development workflow using high-yield cell lines and automated systems, next generation purification resins. It will also showcase best practices and strategies such as phase appropriate quality systems, and integrated drug substance – drug product solutions that leverage standardized technology platforms. Register now!

Webinar
One and Not Quite Done: Gene therapy for Hemophilia
Recorded on: September 3, 2020 | Parexel

The original goal of cell and gene therapy was to deliver a single administration that would maintain therapeutic effectiveness over a patient’s lifetime. This ‘one and done’ model appears to have worked for some gene therapies, where promising follow-up data has been observed. In some instances, however, such as in the case of gene therapy for hemophilia, a single dose may not be enough and redosing may be required. In this webinar, our speakers will discuss: strategies for both one-time and redosing gene therapies, what redosing means for the commercialization strategy, considerations for manufacturing and market access. Register now.

Webinar
Reducing barriers to patient care: A cross-industry collaboration
Thursday, August 27, 2020 | 1pm ET / 10am PT | Optum

Optum brings together cross-industry experts to share a case study detailing how an employer, provider, payer and pharmaceutical company worked together to address a hard-to-diagnose condition: migraine. Register now.

Webinar
CROs: The Tip of the Spear in Maximizing the Value of Hybrid, Virtual, and Synthetic Clinical Trials
Recorded on August 26, 2020 | Rho

Hybrid, Virtual, and Synthetic trials are becoming part of a growing number of drug and biologics development programs. Join us as Rho experts discuss how to maximize the benefits of decentralized trials. Register now!

Webinar
When should your workforce return to the office?
August 26, 2020 | 11 a.m. EST / 8 a.m. PST | Deloitte

Before businesses can recover, they will need to reboot, which will involve developing a holistic approach to managing new health risks, rethinking workforce safety, maximizing productivity, and furthering sales –while protecting and maintaining compliance with privacy and cybersecurity rights. Register now.

Webinar
Navigating CMC Regulatory Requirements for Accelerated Commercialization
August 25, 2020 | 11 a.m. EST / 8 a.m. PST | Lonza

Join us to discuss strategy, timing, process, practical and execution aspects to be considered in order to achieve a target  outcome. Case studies will be presented that demonstrate each of these challenges and the considerations necessary to meet fast-track timing requirements of clinical trials and registration applications. Register now.

Webinar
Powering Virtual Trials – In The Cloud
Recorded on: August 19, 2020 | Amazon Web Services

In this webinar you will hear from technology company uMotif on how they collaborate with pharma companies undertaking virtual and decentralized trials. Hear how new patient populations can be reached using cloud-based technology and learn what types of research data can be collected from different devices and wearables. Register now.

Webinar
Enabling high drug-loaded amorphous dispersion tablets
Recorded on: August 18, 2020 | Lonza Pharma & Biotech

Join us to gain an understanding of how to combine two different polymers, one “inside” and one “outside” the ASD to maximize performance, physical stability, and drug loading of ASD drug products. Register now.

Webinar
Uncertainties With the Regulatory Environment for Continuous Manufacturing
August 12, 2020 | 11am ET / 8am PT | Thermo Fisher Scientific

Continuous manufacturing brings uncertainties with regulatory and adoption rates. Industry expert, Ajaz S. Hussain, PhD, will discuss these uncertainties and provide more insight into this innovation. Register now!

Webinar
Metabolites in Safety Testing (MIST): Analytical Strategy
July 29, 2020 | 1pm EST / 10am PST | Frontage Laboratories

Regulatory agencies have provided recommendations on when and how to identify and characterize drug metabolites to ensure their non-clinical toxicity has been adequately evaluated. The studies conducted to comply with these recommendations are often referred to as metabolites in safety testing or MIST.

This presentation will review the origins of these recommendations and the specific requirements that need to be considered in designing studies to address the regulatory expectations. Register now.

Webinar
Patients can’t wait: Advancing Rare Disease & Oncology drug development during COVID-19
Recorded on: July 28, 2020 | Parexel

This virtual roundtable will explore the challenges and opportunities facing companies developing oncology and rare disease products during the COVID-19 pandemic. Parexel will be joined by Sara’s Cure, a Clear Cell Sarcoma patient advocacy group and charitable foundation. Register now to learn more.

Webinar
Challenges and Practical Solutions for Changing Over to Pre-filled Syringes for Parenteral Drugs
Recorded on July 22, 2020 | Thermo Fisher Scientific

It’s not uncommon for companies who launch commercial drug products in the pre-filled syringe format to do so after initially using other product formats such as vials for the development and clinical trial phases. Switch-overs need careful and strategic consideration because doing so requires investment in the new format but also offers critical patient benefits and improved stakeholder outcomes. During this webinar, you will learn more about benefits and risks of changing primary components during product development and how a design of experiments approach can be used to address issues and risks. Register now.

Webinar
Zero Deviation Mindset: Achieving Agility in Cell Therapy Supply Chains
Recorded on July 21, 2020 | Pluristem Therapeutics & ThermoFisher Scientific

Cell & gene therapy supply chains are inherently complex, requiring the utmost attention to quality, cold chain logistics, and chain of custody requirements. Join Thermo Fisher Scientific and Pluristem Therapeutics as we discuss lessons learned in developing the just-in-time supply chain for their phase III hip fracture study, and how these lessons are being used in their current efforts to treat severe COVID-19 cases complicated by Acute Respiratory Distress Syndrome (ARDS) in the United States. Register Now.

Webinar
BSEPcyte® and MDR3cyte®: Innovative Solutions for Investigating Drug-Induced Liver Injury
July 16, 2020 | 1pm EST / 10am PST | Frontage Laboratories

This presentation will benefit scientists wanting to learn more about DILI and/or those needing guidance on crucial transporter studies for better assessment of DDI potentials that is aligned with regulatory guidance. Register for our Webinar, featuring Kan He, on BSEPcyte® and MDR3cyte®: Innovative Solutions for Investigating Drug-Induced Liver Injury.

Webinar
Becoming the early bird: Establishing a dialogue with the FDA around accelerating preclinical research
Recorded on: July 14, 2020 | Box

By establishing an early dialogue with the FDA—when potential products are still in preclinical testing—companies can gain valuable insights that could boost their chances of success. This webinar will bring together experts in preclinical trial design, R&D efficiency and regulatory affairs to offer advice on how companies can best engage the FDA early in the research process. Register now.

Webinar
EMD Serono & Aktana: Bringing Intelligent Engagement to Every Channel
Recorded on: Tuesday, July 14, 2020 | Aktana

Join this webinar to hear Joel VanderMeulen, Senior Director, N&I Commercial Strategy and Operations at EMD Serono, and Derek Choy, Co-founder and President at Aktana, discuss:

  • Emerging market trends in the post-COVID world
  • How commercial teams can adapt to the “next normal” 
  • The three key components for successful omnichannel engagement

Register now.

Webinar
De-risking the Development of Biotherapeutics Using Early Stage In Vitro Expression and Genetic Characterisation Tools
Recorded on: July 8, 2020 | Lonza

There is a high attrition rate during the development of biotherapeutics impacting the high cost of development. Early identification of the preferred expression host for manufacturing, along with lead candidate screening and material supply can help to reduce both attrition rates and cost.  Register for the webinar to learn more.

Webinar
What Real-World Data Is Telling Us About Managing Patients in a COVID-19 World
June 30, 2020 | 1:00pm ET | 10:00am PT | Optum

In this webinar, Optum will bring together their life sciences consultants, a large payer and pharmaceutical industry experts to share understanding about how patients are managing their medications — and how payers are managing patients — in the ever-changing COVID-19 world. Register now.

Webinar
Restore Elective Procedures in the new normal with Salesforce
Recorded on June 29, 2020 | Salesforce

We are in unprecedented times causing change and disruption like deferral of elective procedures and restricted access to HCPs. In this webinar, you will learn how MedTech companies are planning to rebound from COVID-19 by digitally re-engaging with physicians, HCPs, and health systems as elective procedure volume rebounds. Register now.

Webinar
Scalable protein expression with Pichia pastoris - optimising expression for the highest protein yield
June 25, 2020 10 a.m. EST / 7 a.m. PST | Lonza

In this webinar we will examine a number of the benefits of Lonza’s , XS® Pichia 2.0 including : speed, simple fermentation regimes, robust and scalable processes that can be tuned according to the specific objectives of a program, helping to advance new drug candidates through the development pipeline. We will examine the benefits of XS® Pichia 2.0 by referencing a number of case studies with different molecule formats. Register now.

Webinar
State of Data Analytics and Machine Learning in the Life Sciences Industry: 2020 Benchmarking Survey
Recorded on June 25, 2020 | BHE

This webinar will present the results from BHE's industry survey with FiercePharma on how 100 of your peers are leveraging data analytics to respond to today’s challenges and generate timely, high value insights. The webinar will discuss how data analytics are being conducted across functional areas, how analytics approaches vary according to company size and type, which real-world data sources are most commonly leveraged, and more. Register now!

Webinar
Virtual Series: Clinical Trials
June 22-24, 2020 | Free Virtual Event | FierceBiotech

FierceBiotech’s upcoming series will cover technology’s role in clinical trials. Panel discussions include: the use of sensors, wearables and other remote monitoring devices for tracking patient statistics, real-world data and patient-centric technology, and the role manufacturing plays in clinical trials. Register now.

Webinar
Fail Faster: How Biopharma Companies can Capitalize on Early Drug Development Failures
Recorded on June 19, 2020 | Research Solutions

This Fierce webinar will bring together executives with expertise in biopharma discovery, R&D and clinical trial design to discuss the benefits and challenges of the fail-fast strategy. It will include representatives of companies that have implemented such a strategy successfully and can provide advice on what did and did not work. Click here to register!

Webinar
Human Gut Microbiome-Based Contract Research Applications in Toxicology and Microbiome-Based Drug Discovery
Recorded on June 18, 2020 | Frontage Labs

Register for our Webinar, featuring David Kwok, on Human Gut Microbiome-Based Contract Research Applications in Toxicology and Microbiome-Based Drug Discovery. Save your spot & register today!

Webinar
Rapid and Data-Rich Chromatographic Method Development
Recorded on: June 17, 2020 | Cambrex

Rapid and systematic column and mobile phase screening has become an essential component of method development workflows at Cambrex Durham for NCE APIs and drug products. Utilizing the latest technologies in UPLC, a systematic approach to screening in method development can quickly provide more robust methods earlier in the clinical development lifecycle. Register now.