As we approach mid 2025, the clinical research landscape reflects resilience, innovation, and global rebalancing. Drawing on TA Scan’s June 2025 analysis, here’s a snapshot of trial volume, structure, disease focus, and emerging dynamics compared to last year and the pre-COVID era. Clinical Trial Activity: Strong Recovery in 2025 TA Scan captured a total of 6,071 phase […]
Read more »By integrating medical affairs and unifying communication, Medical Affairs can improve decision-making and patient care strategies.
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The Pharma Crunch: Fewer Resources, Same High Expectations The pharmaceutical and biotech industries are at a pivotal crossroad. Following years of innovation and rapid growth, the sector is now facing a wave of cost-cutting, restructuring, and hiring freezes. From small biotech startups to big pharma, headlines are filled with news of layoffs, budget cuts, and […]
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In today’s fast-paced clinical development landscape, clinical trial data quality plays a critical role — because while data is everywhere, insights are not. Clinical operations teams are under pressure to make decisions faster: Which countries will enroll? Which sites are most experienced? Which investigators are active now? Behind every confident decision, there must be trustworthy […]
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By integrating medical affairs and unifying communication, Medical Affairs can improve decision-making and patient care strategies.
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By integrating medical affairs and unifying communication, Medical Affairs can improve decision-making and patient care strategies.
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Clinical trials are a cornerstone of medical innovation, guiding the journey of novel treatments from laboratory research to clinical practice. Yet, data collection and management can be cumbersome, error-prone, and time-consuming. Electronic Data Capture (EDC) systems have rapidly gained traction as a solution to these challenges. Today, sponsors, Contract Research Organizations (CROs), and research sites […]
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Identifying key opinion leaders and KOL engagement is tougher than ever. Data-driven insights and analytics can give Medical Affairs teams the edge.
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In the fast-paced and competitive world of clinical research, planning trials efficiently and effectively is crucial to success. Yet, the complexity of clinical trial feasibility assessments often slows down the process, especially when teams must harmonize both internal insights and vast external datasets. To accommodate this challenge, we’re excited to introduce TA Scan’s Trial Feasibility […]
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Rare diseases present significant challenges in both diagnosis and treatment due to limited clinical knowledge, small patient populations, and fragmented data sources. Patients often face diagnostic delays, and once diagnosed, treatment options may be scarce or non-existent. Currently, over 90% of rare diseases still lack an approved treatment, underscoring the urgent need for continued research […]
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A single rare disease affects fewer than 1 in 2,000 people globally, but collectively rare diseases impact over 300 million individuals worldwide. The distinct challenges of rare disease trials require innovative thinking and tailored approaches beyond traditional clinical trial planning methods. In this article, we explore these challenges and highlight the creative strategies teams use […]
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Lisle, Il., February 7, 2025 — Anju Software is proud to announce that TA Scan’s Feasibility Flex, has been named a 2025 SCOPE Best of Show Award winner. Recognized by industry professionals at the annual SCOPE Summit, this award celebrates breakthrough innovations that enhance clinical trial operations and feasibility assessments. With over 60 new product […]
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Lisle, Il., January 30, 2025 — Anju Software, a prominent provider of software solutions for the life sciences industry, is thrilled to announce its participation in the 16th annual SCOPE Summit for Clinical Ops Executives from February 3-6, 2025, in Orlando, Florida. In the classic tale of the three little pigs, only one house withstood […]
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In the classic tale of the three little pigs, only one house stood strong against the big bad wolf. In clinical trials, the same principle applies: success hinges on the strength of your trial design and planning. Will your trial crumble like straw or sticks, or will it endure the test of time like a […]
Read more »In the classic tale of the three little pigs, only one house stood strong against the big bad wolf. In clinical trials, the same principal applies: success hinges on the strength of your trial design and planning. Will your trial crumble like straw or sticks, or will it endure the test of time like a […]
Read more »Request a Demo Frequently Asked Questions What is TA Scan? TA Scan is a web-based clinical and commercial intelligence solution, which aggregates, connects, and analyzes global clinical trial, presentation, publication, and diversity and demographic data from the public domain into a single, intuitive database. TA Scan data represents an accurate, comprehensive view of global R&D […]
Read more »Request a Demo Frequently Asked Questions Who can use the Pubstrat MAX system? Pubstrat MAX is ideal for pharmaceutical companies, biotech firms, research organizations, and writing agencies. It supports both internal teams and external collaborators, making it a versatile solution for all types of publication management needs in the life sciences industry. Does Pubstrat MAX […]
Read more »Request a Demo Frequently Asked Questions What is TrialMaster? TrialMaster is an intuitive Electronic Data Capture (EDC) web-based solution designed to streamline Phase I-IV clinical trials. Known for its superior usability and flexibility, it accelerates trial development, improves data quality, and reduces study submission times. What devices can I use to access TrialMaster? TrialMaster is […]
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By integrating medical affairs and unifying communication, Medical Affairs can improve decision-making and patient care strategies.
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Decentralized Clinical Trials (DCTs) are reshaping the future of medical research, offering innovative solutions to long-standing challenges in patient recruitment, data collection, and trial diversity. Considering the FDA‘s recent draft guidance, the focus on expanding accessibility and inclusivity in clinical trials has never been more prominent. In his article, “CLINICAL TRIALS: Need for Accessibility to […]
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Electronic Data Capture (EDC) systems play a pivotal role in streamlining the process of collecting, managing, and analyzing clinical trial data. These software solutions enable sponsors and researchers to digitize case report forms, ensuring efficient data management while reducing the risk of errors associated with manual data entry. Modern EDC systems, often offered through Software-as-a-Service […]
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Access to high-quality data has revolutionized clinical feasibility, making it more robust, accurate, and efficient, and enabling evidence-based decision-making to improve trial outcomes. However, the most successful feasibility studies go beyond data alone—blending clinical intelligence with the real-world expertise of clinical teams in their disease areas. View the webinar with Anju’s experts, Jenna Morris, Executive […]
Read more »Access to high-quality data has revolutionized clinical feasibility, making it more robust, accurate, and efficient, and enabling evidence-based decision-making to improve trial outcomes. However, the most successful feasibility studies go beyond data alone—blending clinical intelligence with the real-world expertise of clinical teams in their disease areas. View the webinar with Anju’s experts, Jenna Morris, Executive […]
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In the world of clinical trials, timelines are everything, with speed to market, regulatory approval, and ultimately patient access to new therapies, all dependent on how efficiently trials can be conducted. One of the most critical factors in clinical trial success is patient recruitment, but with the complex nature of clinical trials and the sheer […]
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By integrating medical affairs and unifying communication, Medical Affairs can improve decision-making and patient care strategies.
Read more »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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Ft. Lauderdale, FL, October 31, 2024 – Anju Software recently introduced Feasibility Flex, the newest feature in the flagship product, TA Scan, designed to transform clinical trial feasibility assessments. This powerful tool addresses the rising complexities of trial design and execution, providing unmatched flexibility and precision to enhance trial planning. Feasibility Flex recently won Best […]
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The field of precision medicine is rapidly evolving, moving healthcare away from a “one-size-fits-all” model to treatments tailored to individual patients. Data science is at the core of this transformation, providing healthcare professionals with the tools to analyze vast datasets that guide the development of targeted therapies. A study in The New England Journal of […]
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Although thousands of clinical trials begin each year, “R&D productivity remains stubbornly low,” write Gaurav Agrawal and fellow researchers at McKinsey. Even with R&D spending up from 44 percent over the decade to 2022, the number of U.S. novel drug approvals has stayed flat. In the face of this challenge, clinical trial managers seek ways […]
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European Society for Medical Oncology (ESMO) Congress 2024, held in Barcelona, provided a unique platform for experts to present their groundbreaking advancements. With over 2,000 abstracts covering immunotherapy, antibody-drug conjugates (ADCs), and clinical trials, the event showcased the future of cancer care and highlighted key therapeutic trends. This analysis is brought to you by TA […]
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Chicago, Illinois – September 25, 2024 – Anju, a leading provider of tailored solutions for the life sciences industry, is excited to announce its participation in the 2024 Society for Clinical Data Management (SCDM) Conference, scheduled for September 29th – October 2nd in Boston, Massachusetts. Celebrating over 25 years of excellence, SCDM’s conference continues to […]
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Chicago, Illinois, September 19, 2024 — Anju, a leading provider of adaptive life sciences software solutions, is pleased to announce its participation as an exhibitor at the upcoming DIA Medical Information & Communications Conference scheduled to take place in London on September 24-25th. DIA MICC brings together medical information professionals for discussions, learning, and practical […]
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Identifying key opinion leaders and KOL engagement is tougher than ever. Data-driven insights and analytics can give Medical Affairs teams the edge.
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MONTREAL, Canada, Aug. 29, 2024 — Valsoft Corporation Inc. (“Valsoft”), a Canadian company specializing in the acquisition and development of vertical market software businesses, is pleased to announce the acquisition of Anju Software (“Anju”), the global pioneer in tailored life science solutions for clinical research, medical affairs, and data science. Anju is a customer-focused organization providing […]
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In today’s highly competitive clinical research landscape, selecting the right investigators is more critical than ever. High physician turnover and growing competition have made it increasingly challenging to maintain successful clinical trial programs. Investigators play a pivotal role in patient recruitment and retention, making strategic and informed investigator selection crucial for ensuring robust study outcomes. […]
Read more »In today’s highly competitive clinical research landscape, selecting the right investigators is more critical than ever. High physician turnover and growing competition have made it increasingly challenging to maintain successful clinical trial programs. Investigators play a pivotal role in patient recruitment and retention, making strategic and informed investigator selection crucial for ensuring robust study outcomes. […]
Read more »View this webinar recording to explore the key features of MA Knowledge, including Smart Filtering, robust search capabilities, and an intuitive dynamic workspace. Through real-world use cases, we show you how MA Knowledge solves common challenges faced by Medical Affairs teams, from curating content to delivering personalized insights. Witness how MA Knowledge empowers your field […]
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View this webinar recording to explore the key features of MA Knowledge, including Smart Filtering, robust search capabilities, and an intuitive dynamic workspace. Through real-world use cases, we show you how MA Knowledge solves common challenges faced by Medical Affairs teams, from curating content to delivering personalized insights. Witness how MA Knowledge empowers your field […]
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Data visualization plays a powerful role in clinical operations. When clinical trial teams can visualize data, they can better contextualize and draw meaning from that information. Insights can then be applied to clinical and research practices. Digital solutions that provide intuitive dashboards, interactive visualizations, and customizable reports can help teams monitor trial progress, identify risks, […]
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Medical Affairs (MA) is coming into its own as the essential communications hub of life sciences companies. As such, Medical Affairs faces an ongoing challenge: How to optimize sharing of information to healthcare professionals (HCPs) and consumers. By implementing digital solutions that foster connections and improve workflows, Medical Affairs teams can reduce their workload while […]
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In a recent Clinical Research News article, Anju’s Vice President and General Manager of the Data Division, Barbara Argibay Gonzalez, shared her thought leadership on leveraging advanced technologies for clinical trial success. Drug development is a lengthy, expensive, and complex process, so the stakes and the risks are high. Fortunately, sponsors, CROs, and innovators can […]
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FORT LAUDERDALE, Fla., Aug. 6, 2024 /PRNewswire/ — Anju Software is proud to introduce MA Knowledge, a mobile application enhancing field rep efficiency by providing meticulously curated medical information. As the newest addition to Anju’s Medical Affairs Suite, MA Knowledge empowers Medical Science Liaisons (MSLs) and field reps by efficiently filtering content to deliver relevant, credible, customer-centric content. […]
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The clinical trials market worldwide reached $80.7 billion in 2023 and is expected to grow at a rate of about 6.5 percent from 2024 to 2030, according to a report by Grand View Research. As clinical trials at all phases accelerate, the need to avoid costly delays and speed time to market is urgent. Automation […]
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Identifying key opinion leaders and KOL engagement is tougher than ever. Data-driven insights and analytics can give Medical Affairs teams the edge.
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By integrating medical affairs and unifying communication, Medical Affairs can improve decision-making and patient care strategies.
Read more »Clinical trials are a highly complex undertaking. Effort in planning and set-up pays off in later management, data collection, and regulatory reporting. With so many moving parts, however, clinical trial teams can be hard-pressed to create a single system or approach that utilizes best practices for every aspect of the trial. In particular, clinical trial […]
Read more »Slash Clinical Trial Build Times In Half With TrialMaster Electronic Data Capture (EDC) Revolutionize your clinical trials by streamlining data collection, processing, and submission to regulatory authorities. Expedite the development and approval of groundbreaking drugs and devices with unparalleled efficiency. Name* First NameLast Name Email* example@example.com Company* Request a Demo Should be Empty: Trusted Global […]
Read more »Clinical trial financial management is essential. Solutions like Anju’s CTMS Master support strategies for budgeting and payments.
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Diversity and inclusion in clinical trials improves trial results. Using data to boost recruiting efforts can help teams reach their DEI goals.
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Data-driven approaches can significantly enhance the strategies of Medical Affairs teams, especially in identifying, engaging, and shaping KOL relationships. Here’s how real-time data access and analytics can impact strategic decision-making.
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Exciting advancements are shaping the future of clinical trials. Anju’s CEO, Larry Birch, was recently interviewed by Moe Alsumidaie from The Clinical Trial Vanguard on the critical role of AI and digital tech in research. Larry shared his insights on integrating AI in clinical research, the importance of diversity, along with the potential and challenges […]
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An advanced electronic data capture or EDC system is essential to maintaining top-quality data integrity during clinical trials.
Read more »In the ever-evolving field of medical affairs, mastering Scientific Communication Plans (SCP) is crucial for ensuring impactful dissemination of scientific information. This webinar, hosted by industry experts, delves into the significance of SCPs, the role of advanced publication management platforms, and the synergistic benefits of integrating your SCP and publication management platform. In this webinar, […]
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In the ever-evolving field of medical affairs, mastering Strategic Communication Plans (SCP) is crucial for ensuring impactful dissemination of scientific information. This webinar, hosted by industry experts, delves into the significance of SCPs, the role of advanced publication management platforms, and the synergistic benefits of integrating your SCP and publication management platform. View this webinar […]
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Check out this insightful webinar recording on the importance of data integrity and efficiency in clinical trials. Explore how Anju’s TrialMaster solution uses real-time data validation to maintain robust data integrity and streamline trial processes. Learn effective strategies to expedite trial builds, optimize data collection, and achieve faster trial approvals. This session will provide valuable […]
Read more »In the ever-evolving field of medical affairs, mastering Scientific Communication Plans (SCP) is crucial for ensuring impactful dissemination of scientific information. This webinar, hosted by industry experts, delves into the significance of SCPs, the role of advanced publication management platforms, and the synergistic benefits of integrating your SCP and publication management platform. View this webinar, […]
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Fort Lauderdale, FL – June 13, 2024 – Anju Software, a trailblazer in comprehensive data and information management solutions for the life sciences industry, is proud to announce its participation in the DIA Global Annual Meeting at the San Diego Convention Center on June 17th-19th. Anju will display its advanced eClinical suite, including TrialMaster and […]
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Predictive analytics can optimize clinical trial design by lowering costs, raising success rates, and speeding time to market.
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In early phase clinical trials, patient safety is critical. eSource solutions like AnjuEPS can help prevent errors and enhance safety.
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Data analysis helps pharma teams understand a complex landscape — and maintain a competitive intelligence edge.
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Digital solutions play a key role in provider engagement. Here’s how HCPs can use these tools to stay informed.
Read more »Request a Demo Bring Life-Saving Treatments to Market Faster Revolutionize your clinical trials by streamlining data collection, processing, and submission to regulatory authorities. Expedite the development and approval of groundbreaking drugs and devices with unparalleled efficiency. Trusted Global Life Sciences Experience 10 of the top 10 GLOBAL PHARMACEUTICAL COMPANIES 16 of the top 20 GLOBAL […]
Read more »Request a Demo Streamline Your Medical Information Management With Our Advanced IRMS Solution IRMS MAX is the gold standard of Medical Information Solutions engineered to deliver what matters most – the right information, to the right consumer, at the right time. Our Experience Makes You Successful 300+ PHARMACEUTICAL, BIOTECH AND MEDICAL DEVICE COMPANIES 100% CUSTOMER […]
Read more »Request a Demo Streamline your Decision-Making With Reliable Data Insights for Increased Efficiency TA Scan is the most intuitive clinical and commercial intelligence solution, aggregating global clinical trial, presentation, and publication data into a single, user-friendly system. TA Scan offers a comprehensive suite of solutions, including the application itself, robust API services, and Data as […]
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With the right digital tools, like Pubstrat MAX, global collaboration on medical publications becomes simple.
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Access to deep data generates better insights in clinical trial feasibility analysis and site selection. Anju’s TA Scan can help.
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Streamlining clinical trials with automated monitoring and reporting capabilities is possible with Anju’s CTMS Master.
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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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How to improve MA decision-making: Give Medical Affairs solutions that help them understand competition and support commercial strategies.
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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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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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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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