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Explore Anju’s AI Roadmap at the 20th Annual Meeting of ISMPP
/Fort Lauderdale, FL- April 23, 2024 – Anju, global pioneer in tailored life science solutions, is proud to announce its participation as an exhibitor at the 20th Annual Meeting of ISMPP, the International Society for Medical Publication Professionals. This year’s meeting centers on the art and science of medical publications and communications, and the power […]
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Improve MA Decision-Making With Advanced Business Intelligence Tools
/How to improve MA decision-making: Give Medical Affairs solutions that help them understand competition and support commercial strategies.
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Anju’s TA Scan Selected by Leading Pharma Company to Enhance Clinical Research
In a significant stride towards advancing clinical research and enhancing patient outcomes, Anju Software, a prominent provider of software solutions for the life sciences industry, has forged a strategic partnership with one of the top 5 pharmaceutical companies globally. The challenges confronted by this pharmaceutical giant encompassed: Ensuring data quality across various therapeutic areas, including […]
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Patient-Centric Clinical Trials: Leveraging Technology for Enhanced Participant Engagement
/As clinical research shifts toward patient-centric models, innovative technological solutions can build bridges between trial participants and researchers. Anju’s TrialMaster incorporates ease of use features, accessibility, and eConsent tools to support decentralized trials and enhance patient engagement
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Updated FDA Race and Diversity Guidance Open for Comments
/The FDA’s draft guidance on race and diversity in clinical trials offers opportunities for clinical trial teams to improve the representation in their clinical trial cohorts — and to extend their efforts beyond questions of race and ethnicity.
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Medical Information Management: Balancing Security With Accessibility
/Making health information both accessible and secure poses challenges in medical information management. Anju’s IRMS MAX helps balance security with accessibility.
Read more »Anju eClinical Webinar: Optimizing Clinical Trials – A Comprehensive Approach
Anju, On-Time Trials, and Barrington James, innovative leaders in the life sciences space, hosted a power-packed webinar designed to elevate your clinical research game. In just under 60 minutes, uncover the keys to success in sourcing, managing, and tracking clinical trials. Expert sessions feature Barrington James shedding light on the role of Clinical Research Associates […]
Read more »Anju eClinical Webinar: Optimizing Clinical Trials – A Comprehensive Approach
Anju, On-Time Trials, and Barrington James, innovative leaders in the life sciences space, hosted a power-packed webinar designed to elevate your clinical research game. In just under 60 minutes, uncover the keys to success in sourcing, managing, and tracking clinical trials. Expert sessions feature Barrington James shedding light on the role of Clinical Research Associates (CRAs), […]
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How Patient-Centricity is Becoming a Cliche and The Crucial Tool in Anju’s Arsenal
/At the SCOPE Summit in Orlando, Outsourcing Pharma’s Senior Editor Liza Laws sat down with Anju’s CEO Larry Birch to discuss where the company is headed, how Anju keeps patients at the forefront while supporting its customers, and the crucial tool in its arsenal. Read the full interview here to learn more on patient-centricity, Anju’s […]
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Vita Global Sciences Announces Strategic Partnership with Anju Software
Fort Lauderdale, FL March 26, 2024 – Vita Global Sciences, provider of professional services for the life sciences industry, is thrilled to announce its strategic partnership with Anju Software, a global provider of life science technologies. This collaboration marks a milestone in advancing technology-driven healthcare solutions, particularly in the realm of clinical trials. Vita and Anju have […]
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Webinar: Optimizing Clinical Trials – A Comprehensive Approach
Anju, On-Time Trials, and Barrington James, innovative leaders in the life sciences space, hosted a power-packed webinar designed to elevate your clinical research game. In just under 60 minutes, uncover the keys to success in sourcing, managing, and tracking clinical trials. Expert sessions feature Barrington James shedding light on the role of Clinical Research Associates […]
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Do You Have a Selection Strategy for Your Clinical Trial Endpoints?
/Choosing clinical trial endpoints shapes the entire trajectory of those trials. The right digital tools can improve endpoint selection.
Read more »Anju eClinical Webinar: Optimizing Clinical Trials – A Comprehensive Approach
Anju, On-Time Trials, and Barrington James, innovative leaders in the life sciences space, hosted a power-packed webinar designed to elevate your clinical research game. In just under 60 minutes, uncover the keys to success in sourcing, managing, and tracking clinical trials. Expert sessions feature Barrington James shedding light on the role of Clinical Research Associates […]
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Anju to Exhibit at MAPS 2024 in Puerto Rico
/Fort Lauderdale, Fla., March 19, 2023 – Anju, a global pioneer in tailored life science solutions, is proud to announce its participation as an exhibitor at the upcoming Medical Affairs Professional Society (MAPS) 2024 conference in Puerto Rico. MAPS 2024 is set to be a gathering of the brightest minds and innovative companies in the […]
Read more »SCDM EMEA24
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The Transformative Role of Generative AI in Regulatory Compliance and MA Communications
/Generative AI offers opportunities to glean deeper insights from data and streamline a number of tasks, including regulatory compliance and many Medical Affairs communication needs. Yet using generative AI in Medical Affairs also poses challenges. Here’s what MA teams need to know.
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Meeting KOLs via Data Makes Initial Communications More Meaningful, Builds Relationships
/Make initial communications meaningful with key opinion leaders by meeting KOLs first through data using tools like Anju’s TA Scan.
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Maximize Product Launch Success with Connected Clinical and Commercial Strategies
/Pharma product launches are more crucial than ever. Here’s how Anju’s TA Scan can help teams connect to maximize product launch success.
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Clinical Trial Costs Keep Rising: How to Fight Back
/The costs to bring a drug to market keep climbing, and the return on investment is dropping. Here’s how to keep clinical trial costs in check.
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Is Lack of Data Integration Undermining Your Medical Affairs Efforts?
/Lack of data integration can imperil product launches, raise regulatory questions, and impede insight generation.
Read more »Clinical Trials in Oncology East Coast 2024
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Read more »BIO 2024
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Read more »ASCO Annual Meeting 2024
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Read more »DIA China 2024
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Read more »Annual Meeting of ISMPP 2024
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Anju to Exhibit and Present at EUCROF24: Leveraging Data for Enhanced Site Selection and Feasibility in Clinical Trials
Fort Lauderdale, Fla. – February 16, 2024 – Anju Software, a leading provider of software solutions for the life sciences industry, is pleased to announce its participation in EUCROF24, EUCROF’s (the European CRO Federation) annual conference. Elke Ydens, Associate Director of Business Solutions at Anju, will deliver a compelling presentation titled “Clinical Use Case: Why […]
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Outsourcing Data Management in 2024: Challenges and Benefits
/Outsourcing data management in clinical trials can provide benefits, yet it also poses challenges. Here’s what to consider.
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The Benefits of Big Data in Drug Development
/Big data is changing the way healthcare is delivered and improving the way drugs are developed. But how exactly does big data benefit drug development? Anju’s Chief Technology Officer Joe Alea recently answered that question in Contract Pharma. Read the full article here to learn more about the emerging role of automation, data analytics, and […]
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Anju Software Unveils Strategies for Data-Driven Decision-Making in Clinical Research at SCOPE Orlando 2024
/Fort Lauderdale, Fla., February 7, 2024 — Anju Software, a prominent provider of software solutions for the life sciences industry, is thrilled to announce its participation in the 15th annual SCOPE Summit for Clinical Ops Executives from February 11-14, 2024, in Orlando, Florida. SCOPE Orlando 2024, a premier clinical operations conference, offers a 200-event exhibit […]
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Time for Clinical Trials to Deliver on Patient-Centric Care Promises
/FDA guidance on DEI and patient-centric care means it’s time for clinical trials to deliver on patient-centric care promises.
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The Importance of Diversity in Clinical Trials: A Comprehensive Analysis
/Why is diversity in clinical trials so important? Anju’s Vice President of Product Management Laura Acosta analyses this below. Her commentary was recently featured in a Clinical Research News article. Read her full, comprehensive analysis below. Clinical trials are pivotal in propelling medical research forward and enhancing the quality of patient care. Yet, for an extended […]
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SCOPE Orlando 2024: The Summit for Clinical Ops Executives
/SCOPE Orlando 2024 offers over two dozen programs and a host of networking events for clinical trial professionals.
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How the Right Software Can Help Small Biopharma Companies Succeed
/Here’s how small biopharmaceutical companies can leverage digital tools for better data management and nimbler decision-making.
Read more »Webinar: TA Scan – Differentiating RFPs
In an era where credibility is paramount, establishing a strong foundation early within a partnership is crucial. This webinar explores how to align data, analytics, and data-driven decision-making to not only adapt but also stand out in the highly competitive CRO market. Anju experts, Elke Ydens, John Coritz, and Mike Loftus hosted this groundbreaking webinar on […]
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Conference Preview: ISMPP Europe 2024
ISMPP Europe 2024 takes place January 23 and 24 in London, offering a host of information and networking opportunities.
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Optimizing Clinical Trial Outcomes Through Predictive Enrollment Strategies
/Clinical trial enrollment calls for new solutions to new challenges. Anju’s TA Scan allows for predictive enrollment for better decisions.
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Webinar: TA Scan – Differentiating RFPs
In an era where credibility is paramount, establishing a strong foundation early within a partnership is crucial. This webinar explores how to align data, analytics, data-driven decision-making to not only adapt but also stand out in the highly competitive CRO market. Anju experts, Elke Ydens, John Coritz, and Mike Loftus hosted a groundbreaking webinar on […]
Read more »Webinar: Online Collaboration with Pubstrat MAX
Do you face challenges engaging authors throughout your publication plan? Are your authors struggling with the time-consuming nature of collaboration? We’ve got the solution! Watch our webinar where we not only showcased Pubstrat MAX‘s cutting-edge Online Collaboration tool, but also shared valuable tips and tricks to enhance author engagement and collaboration. Our hosts, Dan McElwain, Steve Anzuini, […]
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Overcoming Data Management Challenges in Self-Reporting Clinical Trials
/Data management challenges in self-reporting clinical trials versus logged data can be improved, as can harmonizing data types. Here’s how.
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Anju to Showcase Industry-Leading Publication Planning Solution at ISMPP Europe 2024
/Fort Lauderdale, Fla., December 7, 2023 — Anju, a leading provider of adaptive life sciences software solutions, is pleased to announce its participation as an exhibitor at the upcoming ISMPP Europe 2024 conference, scheduled to take place in London on January 23-24. The 2024 European Meeting of ISMPP (the International Society for Medical Publication Professionals) […]
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Optimizing Outreach: Effective Communication Strategies for Medical Affairs Teams in 2024
/To communicate more effectively in 2024, Medical Affairs teams can engage several best practices.
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Medical Research and Publishing Has Exploded: How Are You Managing Knowledge?
/Medical research is too big for any one person to handle. Here’s how Anju’s Pubstrat MAX can help.
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Collaborating With Key Opinion Leaders in Early Clinical Trial Development: Navigating Risks and Rewards
/What are the risks and rewards of bringing key opinion leaders onboard early? Here’s how to support collaborating with KOLs in early clinical trial development.
Read more »BVMA 2023
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Read more »Webinar Replay: Innovative Strategies in Clinical Trials
This webinar on meeting diversity goals in clinical trials, co-hosted by Laura Acosta, Anju’s VP of Product Management, and Elke Ydens, our Associate Director of Business Solutions, explores how regulatory agencies, CROs, and industry leaders are striving to enhance accessibility to clinical trials for under served populations, aligned with the DEPICT ACT’s call for Diversity […]
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How Medical Affairs Teams Can Optimize Product Life Cycle
/ | Leave a CommentThe Medical Affairs (MA) role is evolving from its traditional support role to becoming a strategic force in the pharma community. Indeed, MA teams hold the position as the conduit of medical knowledge and communication among multiple stakeholders. The role of Medical Affairs is now to communicate information about evidence-based medicine within fragmented healthcare systems, […]
Read more »CNS Summit
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Anju Welcomes Atherion Bioresearch as the Newest CRO Partner
/FORT LAUDERDALE, Fla., Oct. 31, 2023 /PRNewswire/ — Anju, a leading provider of life science solutions, announces a strategic partnership with Atherion Bioresearch, a full-service CRO. This collaboration provides both organizations opportunities to accelerate growth, streamline processes, and enhance data integrity. Atherion Bioresearch, established by experienced drug development professionals and focused on helping its partners […]
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Achieving Data Compliance in Decentralized Trials
/Data compliance and harmonization across clinical trials can be challenging to obtain. Here’s how to choose the right tools for the job.
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Breaking Barriers: Meeting Diversity Goals in Clinical Trials through Innovative Smart Trial Design Strategies
This webinar on meeting diversity goals in clinical trials, co-hosted by Laura Acosta, Anju’s VP of Product Management, and Elke Ydens, our Associate Director of Business Solutions, explores how regulatory agencies, CROs, and industry leaders are striving to enhance accessibility to clinical trials for under served populations, aligned with the DEPICT ACT’s call for Diversity […]
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Revolutionizing Clinical Research: The Role of Generative AI
/There’s plenty of speculation about how generative AI could obviate the still largely manual work involved in data capture, medical editing, and medical writing — among several other use cases. But it’s clear at this stage the technology is not there yet.
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TA Scan’s Diversity Module Won Best of Show Award at SCOPE Europe 2023
/ | Leave a CommentJoined by clinical operation teams from around the globe in Barcelona, Spain, Anju Software took center stage at the SCOPE (Summit for Clinical Ops Executives) Europe 2023 conference this week. For the second time this year, Anju’s TA Scan won the attendee-voted Best of Show Award for its expanded European diversity and demographic data. This […]
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Community Pharmacies and Clinical Trial Enrollment
/Here is how pharmacies, and their relationships within the communities they serve, can support efforts to drive clinical trial enrollment.
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Global Diversity Data with TA Scan at SCOPE Europe 2023
/Anju to Showcase TA Scan’s Global Diversity Data at SCOPE Europe 2023 and Compete for Best of Show Award Ft. Lauderdale, FL, October 12, 2023 [PRNewswire] – Anju Software, a leading provider of life science solutions, is pleased to announce CEO Laurence Birch will kick off the Feasibility, Site Selection, and Study Activation program at […]
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The Regulations Clinical Researchers Should Track in 2024
/Worldwide regulations affecting how clinical researchers store, process, and share data are changing rapidly. Here are some of the key regulations clinical researchers need to keep an eye on in 2024.
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Anju Showcases Life Science Solutions at SCDM
/Ft. Lauderdale, FL October 3, 2023 – Anju, trusted partner in delivering tailored life science solutions, is pleased to announce its participation at the upcoming Society for Clinical Data Management (SCDM) conference, taking place from October 8-11, in San Diego, California. For 25 years SCDM has held live global conferences that bring together clinical data […]
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SCOPE Europe 2023: 5 Unmissable Sessions and Insights for Clinical Operations Professionals
/Here are five interesting sessions for clinical operations professionals at SCOPE Europe 2023.
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Streamlining KOL Identification: 3 Tips for Medical Affairs Teams
/Here are a trio of tips for speeding up the process of KOL identification. They include objectives alignment, level of influence and the right software.
Read more »Webinar Replay: Tackling the Challenges of Complex Trials
Our Anju hosts Laura Acosta, Vice President of Product Management, Neil Vivian, Senior Director of Business Solutions, and Caterina Cammalleri, Associate Director of Clinical Operations; hosted a live webinar titled “Tackling the Challenges of Complex Trials” where they discussed challenges with complex trials such as oncology, and how finding the right EDC solution can help […]
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The Role of Site Selection in Promoting Health Equity
/Here is how clinical site selection fits into the larger effort of driving health equity.
Read more »Webinar Replay: Accelerate Publication Approval Process
Within Pubstrat MAX, the Approvals Module is designed so that anyone – internally or externally within a client’s organization – can easily submit a request to have their data or documents approved before sharing with internal teams or disclosing to the public. On September 13th, our hosts Steven Anzuini, Erick Borg and Rachel Sheldon discussed […]
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Preview: 6 Sessions at DIA Medical Information Conference
/The 2023 DIA Medical Information Conference will be held in Brussels from September 27 to 28. These are the six sessions on the agenda.
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Deeper KOL Connections: How Information Design Empowers Medical Affairs
/Here is how medical affairs teams can leverage the tools and the concepts of information design to deepen their KOL connections.
Read more »ISMPP Europe 2024
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Read more »DIA Medical Information and Communications Conference 2023
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Clinical Trial Compliance Auditing: Challenges and Tools
/Compliance auditing demands thorough, complete, consistent information. IRMS MAX is built to provide this data.
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FDA Guidance on Umbrella Trials Can Help CROs Choose the Best Software
/The FDA has issued new guidance on umbrella trials for gene therapies. Here’s how CROs can plan their software choices accordingly.
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Webinar: Tackling the Challenges of Complex Trials
Our Anju hosts welcomed St. Jude Children’s Research Hospital’s Senior Manager-Clinical Research Systems from the Department of Cancer Center Administration Namratha Intha to talk about challenges with complex trials such as oncology, and how finding the right EDC solution can help you meet those challenges. Register here to view the webinar.
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TrialMaster: The Right EDC Solution For Oncology Trials [White Paper]
/Download our white paper to discover the ways that TrialMaster EDC can improve your complex oncology trials.
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How Automated Site Visit Reports Improve Clinical Trials
/Clinical trials require effective documentation. Automating site visit reports with tools like CTMS Master keeps those documents complete and accurate.
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How Medical Affairs Teams Can Boost Stakeholder Engagement
/ | Leave a CommentAnju Software explores what the digital landscape means for Medical Affairs teams and how they can maximize key partnerships and boost stakeholder engagement.
Read more »Webinar: Accelerate Your Publication Approval Process with Pubstrat MAX
Within Pubstrat MAX, the Approvals Module is designed so that anyone – internally or externally within a client’s organization – can easily submit a request to have their data or documents approved before sharing with internal teams or disclosing to the public. Our hosts Steven Anzuini, Erick Borg and Rachel Sheldon will discuss how this […]
Read more »Webinar: Tackling the Challenges of Complex Trials
Anju’s eClinical team is excited to announce their upcoming webinar on tackling the challenges of complex trials. In this session, our Anju hosts: Laura Acosta, Vice President of Product Management Neil Vivian, Senior Director of Business Solutions Caterina Cammalleri, Director of Clinical Operations will discuss challenges with complex trials such as oncology, and how finding […]
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How Patient Voices Power Pharmaceutical Innovation
/Medical affairs teams can leverage their patient access, generate insights from patient voices, and help drive pharmaceutical innovation within their organization.
Read more »SCDM Annual Conference
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Read more »2023 ISMPP Academy
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Rare Disease Clinical Trials: Challenges and Opportunities Researchers Face
/Here’s an overview of the many ways researchers handle rare disease clinical trials challenges and opportunities.
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Clinical Data Analysis: 3 Most Important Frontiers Right Now
/Deep learning, natural language processing, and data standardization are keys that will unlock the future of clinical data analysis.
Read more »TrialMaster: The Right EDC Solution For Oncology Trials
Oncology clinical trials are uniquely complex, logistically and ethically. Practically speaking, they often need mid-study changes and must adapt to subjects’ evolving health outcomes.The most intuitive Electronic Data Capture (EDC) Suite on the market featuring superior usability and flexibility, TrialMaster is your EDC solution for Phase I-IV oncology clinical trials. TrialMaster improves efficiencies and reduces […]
Read more »DIA Global Annual Meeting 2024
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The FDA Race and Ethnicity Diversity Plan: How to Get Researchers Prepared
/Here is what clinical researchers need to know about getting compliant with the FDA plan for achieving racial and ethnic diversity in trials.
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