Best Pharmaceutical and Biotech Software of 2024

AiDEA is an evolution of Customer Relationship (CRM), where Artificial Intelligence forms the basis and engine for operational and analytical solutions powered Microsoft Dynamics 365®. Its native integration of data from multiple sources provides a 360deg customer view, facilitating the implementation and analysis of a true Omnichannel strategy. A solution that is innovative and can support company-wide initiatives with an easy implementation process is the key to success. AiDEA's Intelligent Insights allows AiDEA to provide the right information to the right people at the right time to make the best decision. The solution can be used on multiple devices simultaneously. This allows data and information to be shared in a fluid, immediate and current manner. Strategic suggestions will help you plan your marketing activities to achieve your goals.

Digital asset management for the life sciences industry is integrated and allows global reuse, reducing costs on promotional materials. Marketing teams can easily publish or withdraw content from digital channels, ensuring only approved assets are used. Medical, legal, regulatory (MLR) software is industry-leading and can accelerate content approval and time to marketing. The built-in library of claims with reference links reduces administrative burden and risk when managing claims across channels, countries, and assets. Our industry cloud solutions offer data, software, and services, as well as an extensive ecosystem of partners, to support your most important functions, from R&D to commercial. Veeva helps businesses of all sizes to bring products to market more quickly and efficiently, and maintain compliance.

Eliminate the administrative burdens and delays of contracting and qualifying new suppliers. Instead, you can instantly order from our network of qualified 3,500+ suppliers under a single agreement. We help you automate every task from the moment a project starts, streamlining workflows for stakeholders, milestone management, and request-topay workflows. Our dynamic workflows are customizable to fit your unique buying practices. We simplify payment processing and provide you with robust reporting and analytics tools to track and analyse your spending. You can easily create custom reports to reflect your priorities. Live dashboards allow your team to collaborate, make data driven decisions, and take immediate action.

BeeCTD provides a comprehensive eCTD solution for pharmaceutical companies, regulatory agencies and other organizations. Our modular architecture and transparent licensing policy allows our users to select the modules they want to use: Reader, Compiler, Validator. Full-featured reader that gives you an overview of all the lifecycles of the dossier containing eCTD or NeeS sequences. This includes baseline submissions when transferring from NeeS into eCTD. Realtime, fast, and compliant sequence validator, fully compliant with eCTD /NeeS technical specifications, including. Best practices criteria. Older versions of the eCTD Validation Criteria are also available. Your documents will be compiled in eCTD format. You can use our eCTD tool as a product that allows you to compile your documents yourself, or as a services - we will compile them for you.

Most enterprises are interested in cell production management because they want to be able to control all aspects of production, including sample collection, raw materials, auxiliary materials, equipment and instruments, personnel, the environment, and processes, and make efficient use of their resources. There is no shortage of resources and there are no redundant ones, but the production quality can still be guaranteed. Bio cellmes provides not only problem management but also product tracking, production process management, (including SOP), and QC (product inspection, reagent inspection, etc.). QA (environmental controls, deviation handling, finished products release audit), etc.

BookVision CLM is designed to improve the field engagement of doctors. Present your content to the doctors. Understand what information doctors need. Showcase important items and more. BookVision CLM integrates eDetailing, Remote Detailing, eMail Interaction, Doctor Portal and more. This universe is called Project Multichannel. The Media-Soft Creative Studio department allows us to design content for your CLM Tool. We can create 3D Modeling, comprehensive videos and charts, as well as flashy animations. Booki allows you to easily edit, add, or change your own content. Booki can convert PDF, pots, and other formats to HTML5 to be used on medical rep devices.

The most detailed analysis of data on sales is available today. It can be adapted to administrative and health structures as well as any geographical organization. We collect and process information daily to ensure accuracy in monitoring the market.

A data integration solution for modern science that is science-aware™. The data-driven future can't be built on the legacy architectures and broken data of the past. As research data volumes and types continue to grow exponentially, siloed data management and analytics become more and more unsustainable. For most organizations, however, this data is still spread across multiple systems. If the data has been brought into one place, it's usually done by a separate SDMS tool or business intelligence tool. This does not embrace the central role and highly integrated nature of truly scientific analysis. Jarvis is a science-aware™, data integration solution designed for modern science. It connects and harmonizes all of your collective scientific intelligence including instrument and application data so that you can maximize its value. Scientists can easily access this streamlined insight in a highly searchable living knowledge graph.

A secure platform to develop and share reproducible methods. Central and secure place to organize up-to-date/versionable methods with history and concurrent editing. Create and discover reproducible computational and experimental methods with video, reagents and detailed parameters. Private & secure collaboration with HIPAA compliance. Audit trail, approval/signature (21 Cfr Part 11), 2-factor verification, encryption, VPC and more. A protocols.io Institutional Plan improves productivity, facilitates the teaching process, improves collaboration, and records keeping, and accelerates research progress in most disciplines.

Manufacturers, distributors, 3PLs, and others are facing mounting costs, as well as non-compliance risk, which threatens revenue. LighthouseAI™, a compliance automation solution, reduces your stress and workload while solving compliance challenges. Compliance is achieved within minutes, not in days, protecting your revenue stream against any adverse actions. You can generate immediate compliance assessments and eliminate hours of manual research so you can focus on the most important items. Receive instant regulatory updates, notifications and changes to legislation and requirements that are relevant to your facility. Organize all your data in one place to gain transparency and a bird's-eye view of your compliance.

The XetaBase platform is unique in that it simplifies tertiary analyses by aggregating, indexing and enriching secondary genome data. This allows for a continual reinterpretation of the data to unlock clinical and research insights. XetaBase enables the rapid management of genomic data and its cost-effective use in the laboratory and clinic. XetaBase is a genomic-scale platform. The greater the volume and the complexity, the better the insights and outcomes. XetaBase, a genomic-native platform, is built on the OpenCB open-source software platform. It meets the demands of genomic medicine for speed, scale, and reinterpretation. Zetta Genomics provides genomic data management that is fit for the precision-medicine age. XetaBase offers a novel solution for the challenges of genomic information. It replaces outdated flat file approaches and brings meaningful and actionable genome data to the lab and clinic. XetaBase allows for continual reinterpretation and scales seamlessly as databases expand to include genome sequences.

Ideagen PleaseReview is a document-review, co-authoring, and redaction software program that allows you to manage and control all aspects of the document creation process. It delivers: - Improved operational performance, productivity, and efficiency - Better compliance and business oversight - Mitigation and mitigation of regulatory, legal, and commercial risk Save valuable time and effort in conducting document reviews, get rid of tedious admin and have all comments, changes and discussions from multiple reviewers documented in one place. All contributions are even recorded in a comprehensive reconciliation report ready for auditing. You’ll never look back.

Regional Analyzer, the only Business Intelligence product on the market, allows you to evaluate your promotional investment on a regional basis. Evaluate the response of your promotional investment to the region. Compare the results and efforts in different zones and markets. Create a structured ranking based on the prescription market share of the area to evaluate. Periodic evaluations can be conducted by separating results at intervals that are customized. Integration solution that can be used without an Internet connection.

Analysis of prescribing doctors based on your market (speciality, region, healthcare coverage) and healthcare coverage. Identification of doctors that have been visited or not. The Rep's can access the prescription records of each professional based on the "filters" they have created. View the physician's file and quickly recognize the prescription profile. Access a ready-to-use automated and quality integration system. Platform with multi-devices design. It can be used on Smartphones, Tablets, iPads, and computers.

Hundreds of thousands of base pairs can be assessed in seconds. Check orders at checkout to prevent misuse. Verification of licenses, registrations, biosafety and legal use. Save time by avoiding back-and-forth conversations with your customers. We perform all compliance checks during checkout. Aclid can help you avoid order cancellations or delays due to lost emails or slow responses. Our platform streamlines compliance by managing customer follow up. All your data is in one place, so you can respond to fewer false alerts. Let us manage your biosecurity processes while you grow your company. We keep up with new regulations, guidelines and research. Aclid is a powerful platform which manages the whole process. It also offers in-house support that will guide you.

AmpleLogic Regulatory Tracker is built using the LOW CODE AND NEUTRAL CODE (LCNC PLATFORM) and consists of two modules: ANDA Tracker and DMF Tracker. This Pharmaceutical RIMS Software will help you improve data quality, increase operational efficiency, reduce mistakes, and streamline communications across departments.

AmpleLogic’s Learning Management System is designed to organize, monitor, and track a wide range of GMP and Non GMP training for life sciences, pharmaceutical manufacture, API (Active Pharmaceutical Ingredients) Manufacturers, Contract Development and Manufacturing Organization (CDMO), biotechnology, and Contract Research Organizations (CRO), including SOPs, technical, HR and external training. AmpleLogic Pharmaceutical Training Management Software helps determine training requirements based on the role of an individual. It is also possible to create department-specific training schedules, implement and assess different forms of employee training, ensure compliance through appropriate tracking and keep training records with the creation of annual reports for management review.

AmpleLogic EDMS Software, a powerful electronic document management system, is designed exclusively for Pharmaceutical and Biotech Companies. It was developed and implemented to meet the cGMP requirements of Pharma domain, with 21CFR Part 11 Compliance, EU Annex 11 Compliance, which can easily eliminate the challenges faced by various companies. AmpleLogic EDMS, a paperless system for document management, allows you to manage all documents and information with ease. AmpleLogic Document management system includes a variety of activities such as document creation, review and approval, editing, document comparisons, version control and parallel reviews.

AmpleLogic's Quality Management Software is designed to meet the strict requirements of industries that are heavily regulated. The ISO 9001-certified cloud-based Quality Management System is ideal for Lifesciences and other industries such as Food & Beverages, Cosmetics, Medical Devices or Gene Therapy. Businesses are adopting QMS solutions as they recognize the challenges of manual quality checks, which can be laborious and prone to errors. These systems are crucial in improving audit quality by automating processes, managing data efficiently, and integrating APIs.

ActivityBase is a proven industry software platform that manages screening data. It has a number of data analysis tools as well as built-in tools for registering objects and compounds. ActivityBase provides analysis for a variety of biochemical, cellular, and biophysical assay formats, including Ion Channel, FLIPR (Fluid Ionization Potential Resonance), Kinetic, SPR (Selective Pulse Response), and Mass Spectrometry. The system can be easily integrated into HCS imaging stores, such as Perkin Elmer Columbus (Thermo Fisher HCS Studio), Molecular Devices MDCStore, for easy data and image import. ActivityBase includes a built-in compound registration tool and plate management tools. ActivityBase allows you to easily track and manage results from years of tests in one system. The system can be configured according to your needs without the need to purchase new analysis packs. By improving your data analysis process, you can even tenfold your lab analysis.

Basil uses advanced AI and machine-learning technologies to speed up access to vital insights that drive success in medical product development. Basil unlocks intelligence from multiple disconnected data sources in a powerful SaaS platform. You can then make better decisions faster, accelerating time to market, optimizing your product strategy, driving innovation and mitigating risk. Find answers and insights for your regulatory strategy with greater efficiency. Discover vital insights into in-market quality, surveillance, and trends, which are otherwise unavailable. Discover, explore, and analyse over 500k clinical trials to gain a better understanding of the existing clinical evidence.

Global life sciences industry trusts us to drive intelligent engagement. Intelligent HCP engagement across all channels in real-time can improve customer experience. Data science and embedded intelligence can be used to provide customers with the most relevant and effective messages. Field teams should have access to the most current information and insights in order to plan and execute calls. Compliant note capture can help you build deeper customer relationships. Pre-built and custom visualizations provide tailored insights at the point where execution takes place. Veeva CRM allows commercial organizations to use artificial intelligence in the way they choose. Veeva CRM Suggestions is an open model that allows you to implement the best actions with any data science provider.