Alternatives to LifeSphere RIMS

RegDesk is the most comprehensive AI-enabled RIMS platform for Medical Devices, Pharmaceuticals, and IVD companies. • Our proprietary Regulatory Intelligence for over 120+ countries is translated and accessible in a standard format. In addition, it provides alerts on evolving regulatory changes • Our AI-powered Application Builder allows RA teams to prepare and publish global applications in 1/10th of the time • Our Change Assessment capability helps RA teams understand the impact of the change(s) on an existing product(s) and the action required • Our Distributor Collaboration provides seamless workflow solutions to interact, communicate, and share documents with external business partners • Our Standards Management makes it easy for RA teams to search and manage not only international but also country-specific standards • Our Tracking & Reporting functionality allows teams to track regulatory projects across the globe, receive renewal notifications, and generate reports on KPIs within seconds For more information, visit our website.

Adaptive Compliance Engine® (ACE®) is a highly configurable, workflow based eQMS/eDMS and more that can adapt to any business process, allowing for real-time tracking, management, and reporting of all compliance, quality, and operational activities. With ACE®, you will minimize the administrative hassles and maximize ROI with productivity gains from day one – all while 21 CFR Part 11 compliant. Our one-stop software includes: -Office 365 Integration -Inspection Management -Document Management -Risk Management -Product Lifecycle Management -Learning Management -Audit Management -Quality Events -Paperless Validation -Electronic Signatures (21 CFR Part 11 Compliant) -Endless Workflow Configurations -And so much more! Empower all levels of your organization with intuitive user interfaces, easily search for all your documents and records, and transform your data into actionable intelligence with advanced analytics all on a single platform. ACE comes with everything you need, all included at one price. Every application is included, no more a la carte pricing. No more nickel and diming. One software, endless solutions.

Essenvia delivers business value to all departments and teams, and increases efficiency across the board. Centralized repository of all regulatory information allowing collaborative authoring, reporting, and eliminating technical holds, RTAs and RFIs. The regulatory affairs department is empowered to accelerate product launches, and eliminate revenue losses due to delays in submissions and missed renewals. Helicopter view over the entire regulatory lifecycle. Executive dashboards, metrics and proactive alerts are available for global registrations and submissions. Essenvia, a RIM Platform, allows you to manage regulatory workflows throughout the entire product lifecycle. It also accelerates global market access and generates exponential business value. Consolidate all regulatory activities onto one platform to bring your devices faster to market. All registration documents linked to product master information are stored in a central repository. Manage the product registration lifecycle per country.

It can seem like a never-ending series of tradeoffs to bring breakthrough products to market within highly regulated industries. MasterControl's GxP software simplifies workflows, so you don't have to compromise quality for cost or innovation with regulation. Complete and connected meets flexible and fast. MasterControl Quality Excellence transforms quality data and processes to a competitive edge. Modern software is the first step in modernizing your manufacturing operations. MasterControl Manufacturing Excellence, from work orders to production records (EBR/eDHR), to logbooks and work instructions, is the easiest way to digitalize manufacturing.

RegDocs Connect provides the tools for your regulatory and operational teams to create compliant, submission-ready documents and records. This solution is built with the end user in view. It focuses on collaboration, automation, and quality. Automated workflows allow you to manage your records from draft to final. This allows your team to have complete control over your regulatory documents at any time. The mapping of document types to the EDM Reference Model and eCTD allows for organization and retrieval of documents that can be used in regulatory submissions. The powerful tools of PDF/A Publishing, document classification, unique document identifiers, and EDM reference model facilitate regulatory document management. This solution pulls together information from all levels of your organization into one easy-to-use solution. The ability to produce submission-ready and quality content has become more difficult due to electronic submissions to regulatory authorities and the complexity of drug development.

Rimsys provides a single, cloud platform for end-to-end regulatory process digitization and automation. Designed by and for regulatory affairs professionals, Rimsys helps medtech companies reduce repetitive administrative work, speed time to market, respond faster to changing regulations, and drive alignment across internal teams, affiliates, and partners. Only Rimsys provides a holistic platform that supports a full range of regulatory activities. Use regulatory intelligence and digital templates to guide regulatory strategy and streamline submissions. Create compliant, submission-ready content, and consolide PDF packages for electronic and print submissions. Digitally collect and maintain evidence of compliance. Link to relevant standards and get notified of changes. Get notified of changing standards, laws, regulations, and guidance documents that impact your products. Create self-service application, product, and country reports to see exactly where your products can be sold and their current registration status.

Kalypso offers life sciences companies a cost-effective accelerator to implement a RIM system - Accel for RIM. The integrated platform allows for efficient product distribution and management, as well as a global platform to track and manage product registrations. It consolidates compliance data and quality data from different enterprise solutions into one global source of truth to facilitate product registrations and tracking in order to speed up regulatory submissions. Modern APIs are used to combine product data, regulatory documentation, and submission packages. Pre-configured for quick implementation with a valid software system. Based on industry-leading RIM practices.

End-to-end regulatory information management from a single platform. The Vault RIM Suite streamlines global regulatory process on a single cloud-based platform. This allows life sciences companies to increase visibility, data quality, agility, and efficiency. You can respond faster to changes in regulations and improve process efficiency, from submission planning to publication. Coordinate regulatory efforts across HQ and affiliates within a single RIM platform. Assure that teams are creating reliable regulatory content with high data integrity. Veeva Vault Registrations manages product data worldwide, including variations, registration status, and interactions with health authorities. Veeva's flexible data structure supports IDMP data points, and will continue to support changing regulatory data standards. Veeva Vault Submissions automates regulatory process steps and streamlines submission planning.

Global regulatory affairs system that includes registration management software and support from regulatory experts around the world. This registration system is required to renew, amend, transfer, or modify your IVD market access approval or medical device. The intuitive user interface of LICENSALE®, which includes real-time data and infographic analytics, allows for project management, collaboration, future market access planning, advanced reporting, and effective project management. It allows you to take control of your global medical technology registration activities. Arazy Group's "in-country regulatory experts" review your compliance documents and assist in the preparation of your applications. They will work with authorities until you receive your desired marketing approvals. LICENSALE®, which includes compliance and submission requirements for your product in over 140 countries, as well as regulatory experts to help you with each market.

Imagine all your regulatory information about products, registrations and submissions, correspondence, and commitments in one central place, accessible from anywhere. Ennov RIM allows life sciences companies to streamline their regulatory processes, improve data quality, quickly respond to business-critical questions, and effectively responds to health authority requests. Ennov RIM, a purpose-built application based on Ennov Process, allows for the tracking and management of therapeutic product details as well as registration information. Ennov RIM gives regulatory personnel the essential information and functionality they need to manage product portfolios globally, whether you're planning to launch a new product or handle variations to existing registrations.

DXC RIM platform manages regulatory content, data and workflows in one central place. This helps teams accelerate innovation and reduces time to market. A unified platform is required to manage regulatory data and workflows due to the sensitive nature of regulatory affairs content (RA). All relevant data must be easily accessible to all teams. They also need an intuitive, customizable user interface that is simple to use. While configurable reporting and collaborative tools are essential for success, legacy technology can frustrate teams or slow down processes. Compliance is difficult. It is difficult to collect data and document processes. Life sciences organizations that use disparate technologies and have fragmented legacy systems can create problems. They may need to resort to spreadsheets in some cases to manage key operational processes. A centralized enterprise-grade solution is required to bring products to market and manage RA.

RIMExpert™, which addresses regulatory planning, tracking, and data management, manages the global rollout plans and automates the creation of regulatory activities, medicinal products, and regulatory applications. RIMExpert™, reduces data entry requirements, improves data quality, and increases global oversight and control. Standardize regulatory planning, tracking, and registration management processes. Increase collaboration between affiliates and headquarter. All registration activities can be done in one place. One point of contact for all applications, questions, correspondence, and commitments. To maximize the efficiency of enterprise regulatory resources, sync your efforts. You can monitor registration activities throughout the product's lifecycle, keeping track of deadlines, status of commitments, and agency questions. Interactive dashboards to monitor and control regulatory activities and registrations.

PhlexRIM dramatically improves compliance by providing you with real-time, efficient and effective access to your global registration information. PhlexRIM 2.0 includes a library of pre-configured automation "bots" and built-in regulatory use case examples based on industry best practice. The intuitive drag-and drop design tool allows regulatory teams to automate their business processes without the need for programming knowledge or IT support. Manage the entire lifecycle of pharmaceutical product registration activities. Access detailed status information and make use of the alert management feature that is part of all workflows. You can either use standard reports to illustrate your reports or create your own reports. You can create and assign regulatory tasks to your organization for management, headquarters, and affiliates.

Samarind RMS is a smarter way for you to manage your medical product information. Samarind RMS allows you to only enter data once, and you can reuse it as often as necessary. An example of this is the 'INN' which can be used once and reused for all IMA submissions, renewals and variations. This concept is applicable to all key data within the system. It has been proven to improve data quality and streamline workflows. Our pragmatic approach to systems design and implementation means that our customers can manage their licenses smoothly and efficiently, safe in the knowledge that our single-place-of-truth™ approach for regulatory affairs professionals delivers a complete end-to-end system. An electronic document management system (EDMS), which includes version control, template creation, and the ability to link with external document management systems like Documentum™, SharePoint™.

Freya is an advanced AI regulatory assistant that simplifies the process of understanding and navigating complex regulations. By leveraging a vast database of over 40,000 global regulations, Freya provides real-time, verified answers to regulatory questions and offers tools like document translations and summaries. The platform supports compliance management by offering up-to-date regulatory information, ensuring businesses stay informed and efficient. Powered by AI and verified by industry experts, Freya enables organizations to make faster, more accurate decisions while managing their regulatory obligations across multiple markets.

ViSU™, a cloud-based End-to End Regulatory Information Management platform (RIM), is specifically designed for the medical device industry. It allows global users to access and manage regulatory data (Product Master and Registrations, Tracking), Dossiers/Tech files (Submission planning and building & lifecycle), HA/NB correspondence and Obligations tracking. ViSU helps you embrace digitalization in regulatory. It provides connectivity, traceability, and automation which leads to regulatory management efficiency, lower compliance risks, and cost reduction.

High-cost contributors are essential for regulatory functions. They can be found in a wide range of regulatory content. This problem can be solved by a cloud-based solution like Infosys' regulated document management platform. Externalization, collaborative authoring, and editing. Simplify governance and processes; implement a consumption-based model. Support audit trails. Implement a proven solution that guarantees 99.95% uptime in production. Our solution allowed business users to search documents in a vast repository in just 3/4 seconds. Users also had unlimited storage on-demand. To reduce operational and maintenance costs, the DMS uses Google's application programming interfaces (APIs). The company's overheads are restricted to API usage and storage space.

IQVIA Smart, our new end-to-end regulatory information management software, streamlines regulatory processes. Your team can focus on delivering high-quality products to the market instead of labor-intensive maintenance. RIM Smart, the modern regulatory information management system, is designed to improve speed, collaboration, efficiency, visibility, and performance across your entire global portfolio. It also reduces costs. IQVIA RIM Smart is a secure cloud-based solution that allows for interconnected, comprehensive, and intelligent management of all regulatory processes. IQVIA safety platform integration will increase performance and improve flexibility. Automate manual processes and increase connectivity to improve efficiency, cost savings and coordination as well as cross-enterprise visibility and visibility.

Our enterprise document management software is the best in its class. Meridian offers a single source for truth and configurable workflows that streamline collaboration with all departments. It also ensures that every document change is versioned, audited, and reported to the regulatory authorities. Engineering document management refers to the process of finding, finding, and managing complex engineering documents, including CAD files, drawings, technical documents, and communication documents, in AEC organizations (Architecture, Engineering & Construction). Businesses in these industries can find it difficult to manage their engineering documents effectively. Meridian's document management software for engineering projects can address these concerns. Meridian can centralize documents and drawings within an organization while automating key processes.

New revenue opportunities can be found through reliable, real-time data and predictive insight. Controlant's platform provides actionable insights into supply chain performance and automates workflows and processes. You can access the entire supply chain from your mobile or desktop. It is a simple and efficient source of supply chain truth. There are no gateways or manual USB upload. Your data is yours. You can view and report on the chain of custody to assist with regulatory compliance and audits. Ensure that your products are safe and sound at every step. Streamline processes to reduce product and operational waste. Smart analytics can help you achieve measurable ROI. Data analytics can be used to identify and mitigate risks through process improvements. You can identify and implement strategies to reduce waste and carbon footprint. A cloud-based intelligent software platform that delivers on-demand supply chain insights and predictive analysis.

PharmAssist provides a robust Distribution Management solution that can manage all the needs of wholesale and distribution businesses. It will give you an edge over other solutions. It is easy to use and organizes all business activities, including delivery, collection, tracking, and orders. This makes it seamless. It also offers fast billing and an organized and scientific stock arrangement that allows for faster stock removal and delivery. Our goal is to streamline, automate and optimize the workflow of our clients, primarily those in the healthcare and pharmaceutical sectors. We use a proactive and collaborative approach. Our primary focus is to assist pharmaceutical companies in managing their distribution and retail operations. This includes tracking the entire sale life cycle of pharmaceutical products, from the manufacturer to the distributor and retailer, and ending with the customer.

We are accelerating the development of innovative solutions to benefit all healthcare stakeholders. This will help to increase access to therapy, decrease prescription abandonment, and improve patient outcomes. We are committed to removing healthcare access barriers, whether that's by resolving prior authorization issues or increasing awareness about support services. Healthcare is becoming more expensive than ever. Assist your patients with their prescribed therapy by finding affordable solutions that will help them with high-deductible plans, increased copays, and lack of visibility. Some patients find that staying on their therapy is the most difficult part of their healthcare journey. This could be because they don't know how to take their medication or remember to do it at the right time. These adherence challenges should be addressed with people-first solutions.

ClinChoice manages global regulatory data with technology expertise, a deep understanding and best data management practices. ClinChoice uses its expertise in technology and regulatory affairs to help organizations manage their regulatory information. Our consultants offer general data maintenance support in regulatory Information Management System (RIMS) software. This will help ensure that applications are submitted, approved, renewed, and tracked on time. We offer the necessary support in managing and controlling the drug registration process. This allows drug and medical device manufacturers to track all regulatory information and has the ability to see it. Organizations can develop short-term and long-term strategies that meet submission deadlines with minimal impact on their day-to-day operations.

The regulatory affairs departments in the healthcare and life science industry are driven to improve efficiency and create intelligent systems that optimize costs, maximize accuracy, and reduce submission times. RIMTrack, a cloud-ready, artificial intelligence (AI)-based, new age regulatory information management system, addresses this concern. It was created from scratch to assist organizations in preparing submissions accurately and efficiently. It streamlines regulatory processes related to licensing, approvals, regulatory, competitive intelligence, clinical trials and reporting across global stakeholders. Integrate with existing RIM systems to achieve complete management of the regulatory lifecycle process.

Alpha Clinical Systems' electronic Drug Inventory Management System (DIMS) will help you improve study efficiency, regulatory compliance and patient safety. Reduce site errors, workload and gain real-time visibility. ez-DIMS is a comprehensive web-based solution that streamlines drug and equipment distributions on site, eliminating transcription errors. Integrated with ex-SourceDocx to automatically account for supply disbursements and provide real-time visibility on drug inventory. EZ-DIMS is a user-friendly alternative to manual, slow and error-prone processes. Scanners that are easy to use can reduce site workload by accurately and quickly recording study supply inventory at the patient, study site and study level. The second most common regulatory inspection findings are drug inventory violations on the site. Reduce medication assignment/dispensation errors by leveraging QC cross-checks between ez-DIMS and ez-SourceDocx.

All the information you need to register your IVD product or medical device in any market worldwide and manage your market access licence throughout the product's life cycle. REGISLATE®, which provides information about medical and IVD device-specific submission file requirements for each country, allows users to manage their market access licenses through the product life cycle. You can track milestones, timelines, estimated and actual completion dates, as well as estimated and actual completion dates, for initial registrations, renewals, amends, and license transfers, in real-time. For clear monitoring and management, infographic data and proprietary indicators are available. Collaboration tools are available to assist with the preparation and review submissions, compliance requirements, and documents. Receive progress reports in real time for current and future submissions, including market access readiness index. REGISLATE®, which includes GR-MAP registration tracking, for both country AND product.

Every click is an opportunity to make mistakes. Formweb reduces patient risk by combining all the information your doctors need to quickly and safely prescribe medication in one easy-to-use site at the point. These resources can be difficult to find with other pharmacy formulary tools. Your formulary software can save lives. Formweb is not only designed to meet regulatory requirements, but also to save you and your hospital money and time. We are the formulary experts and can simplify the search process. This will save you time, decrease calls to the pharmacy and help with compliance. But most importantly, it will reduce risk and improve quality of care.

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.

OpenText™, a leading provider of information management solutions for life sciences organizations, helps them to harness insights from data and content to improve their decision-making and accelerate product development. Integrate, manage and securely exchange data between people, systems, and things. Use information assets to drive innovation and commercialization. Cloud-native software can run anywhere, giving you freedom of choice. OpenText for life sciences accelerates discovery by delivering actionable insights that can be used to drive innovation in pipelines. Intelligent capture allows you to capture and manage research papers in electronic lab notebooks. Text mining can help you gain insights. Unstructured text in clinical trial reports, study protocol, clinical safety and efficiency findings, can be used to extract knowledge. Learn how to intelligently analyze and classify clinical trial documents and extract them to reduce the risk for costly stops and starts.

GHX Exchange Enterprise modernizes healthcare supply chains through standardization and automation. Traditional providers managed the order cycle and their growing staff manually. This can lead to higher error rates and lower performance. GHX Exchange Enterprise digitizes all aspects of the cycle for better efficiency, connected supply chain data, and better performance insights. GHX gives healthcare organizations a better understanding of their supply chains and how they are delivering on their business goals. GHX Exchange Enterprise automates transactions in order to reduce errors in data entry and administrative costs. This helps to generate more accurate data that can be used for supply chain improvement and decision making. GHX Exchange Enterprise can help you manage your processes, improve data quality and accuracy, and improve overall performance.

Speed Script PRM is an all-inclusive pharmacy management software, Speed Script POS is an integrated point-of sale system for managing your front end sales, and Speed Script LTC(SSLTC) is an electronic facility to pharmacy communication app - fully equipped for drug pass and eMAR technology. Our defining characteristic has been and remains our commitment to exceptional customer service for over 40 years. Speed Script PRM was designed with today's independent pharmacy mind. The speed script prm system integrates features such as text messaging, electronic document storage, management, mobile delivery app and accounts receivable/in house charge accounts. Custom reporting is also available.

Calyx understands that data is key to the success of any clinical development program. Your electronic data collection (EDC), system is crucial to your success. Calyx EDC is used in more than 2,600 clinical trials around the world. It streamlines data collection and reporting through one platform. Don't give your sensitive data to anyone. We can help you make your program a success with Calyx. Calyx EDC allows you to plan, design, and carry out studies of any complexity. Calyx EDC helps you keep your trial on track with features that reduce costs, improve site visibility and drive efficiency.

Saveo is a one-stop shop for all your pharmacy requirements. Saveo is an online B2B marketplace for pharmacies that brings primary and secondary medicine markets together. It offers faster delivery, cheaper procurement, and better technology. Its goal is to ensure that no prescription will bounce in India. The Indian pharmaceutical industry has a high level of fragmentation with 6.5lakh retail outlets and 65000 distributors. This is in contrast to the US, where there are only 5 major distributors that cover 93% of the market. We want to streamline the supply chain and empower these 6.5lakh entrepreneurs with technology and sustainability. Saveo is on a mission of empowering traditional pharmacies through a reliable, scalable and efficient healthcare supply chains.

Pharmacy owners face a number of challenges today, including managing a wide range of products and managing drug shortages. They also need to ensure that they are in compliance with DSCSA and their vendors. SureCost's pharmacy inventory management and purchasing software solutions will save you money and time so you can successfully navigate these complexities. SureCost is a smarter purchasing solution. Our pharmacy customers save an average of 2-5% on their cost-of-goods year over year. Bring your entire catalog together into one seamless solution to save your pharmacy thousands of dollars and thousands of hours every year. SureCost's inventory and compliance management solutions enable you to manage your vendor and DSCSA compliance, unify your purchasing and inventory and work smarter. SureCost unifies your pharmacy inventory and purchasing, so you can optimize buying decisions and find money-saving opportunities by using your entire wholesaler and vendor catalog.

UNISOLVE is a leading software solution for pharmaceutical distributors and wholesalers. UNISOLVE is a future-ready system that automates numerous wholesale operational processes, such as order management, inventory management, data accounting, and other financial transactions. With advanced capabilities, it ensures timely, proper delivery of items. It has been the best-selling software in the pharmaceutical industry across the country for over 27 years and meets all of the industry's needs. UNISOLVE software can help pharmaceutical wholesalers and distributors to run their businesses with less staff/resources. It is a completely precise and reliable solution for all of their requirements that is also cost effective.

MedEx is an integrated suite of solutions for controlling, securing, and tracking the preparation and distribution medications and supplies. We are the most comprehensive hospital workflow solution on the market. We improve compliance, efficiency and safety from preparation to delivery. Ultra-high-resolution imaging is our answer to enabling faster tracking and replenishment of medications used in pre-configured trays and kits. Instant image capture identifies and alerts staff to missing, misplaced or expired medications. This helps guide and speed up proper replenishment of a safe configuration. You will save time, patients will be safer, and you will receive the metrics that you need to optimize your tray and inventory management. You can choose to process using a kiosk or a mobile device. Visual confirmation of medication placement by using 2D instead of expensive RFID tags.

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.

Antares Vision Group developed a digital solution for drug and medical device logistic automation. This eliminates or reduces non-value-added activities for patients while introducing a paradigm shift in process efficiency for healthcare providers. The Medication Management Platform eliminates nonvalue-added tasks that can help hospital systems optimize their time so they can focus on patients and patient safety. The Medication Management Platform enables complete traceability of the movement of medicines and medical equipment, and can be combined with automation systems to improve efficiency and operational excellence in healthcare institutions. Traceability and automation systems combined allow for better management of reorders, stocks and reorders, both at central and peripheral levels. This helps to avoid waste due to expiration.

Dow Jones Risk & Compliance, a global provider, provides best-in class risk data, web based software applications, and scalable due-diligence services to help organizations manage risks and meet regulatory requirements in relation to financial crime, third party risk management, international trade, and sanctions. Dow Jones Risk & Compliance is built on the legacy of the world's trusted newsroom. It combines the expertise and knowledge of a multilingual team of researchers with the industry-leading data scientists, technologists and analysts to provide actionable compliance content. Our solutions were created in partnership with leading legal and political advisors, including former regulators, to help our clients maintain consistency among global business units and teams.

The delivery service is no longer a "nice-to-have". Your patients expect to be able to receive their medications at home, and pharmacists are more than happy to oblige. However, medication deliveries require a few extra steps. PrimeDELIVERY offers secure, on time medication deliveries that comply with all regulatory requirements. The records are seamlessly transferred back to PrimeRx. All prescriptions that are set up for delivery in the pharmacy system are marked "out for deliver" Once the prescription is delivered, the system will update the patient's record to "delivered". Undeliverable medications are automatically returned to stock and the stock levels are automatically adjusted. The system sends a request for an electronic signature to the patient in advance of a scheduled delivery. The patient signs and PrimeDELIVERY sends it back to the pharmacy.

Know how to distribute and optimize your product in pharmacies. Segmentation of pharmacies based on your market. Evaluation of the quality distribution of your product by pharmacies. Evaluation of coverage using a numerical or weighted scale. Mapping of additional sales opportunities from a distribution that is enhanced. Definition of a marketing strategy to increase sales. Your commercial team's orientation and size. Distribution diagnosis in pharmacies helps define distribution targeting, and product placement. Ideal for the launch stage and maturation stages.

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.

SANeForce offers a comprehensive CRM and sales force automation solution, primarily tailored for the pharmaceutical, healthcare and life sciences industries. SANeForce is designed to increase the productivity of marketing and sales teams. It offers features such as real-time order tracking, expense tracking, stock control, and territory administration. The platform supports medical representative reporting, allowing field sales personnel log visits, capture doctor interaction, and manage appointment directly from their mobile device. SANeForce's data-driven insights, analytics, and customer engagement strategies help organizations track performance, streamline their processes, and optimize their customer engagement strategies. The solution also includes features for compliance, making it an ideal choice for highly-regulated sectors that require meticulous records and adherence to standards.

SupplyMover is the ultimate CRM, e-commerce, and sales enablement suite designed exclusively for distributors. Manage all your operations effortlessly in one intuitive platform, equipped with industry-specific tools. Easily access and organize your data in seconds, and benefit from AI-powered selling suggestions, an online shopping portal, customer and product management, analytics, workflow automations, automated lead management, and more. Create the perfect workspace for your distribution industry and roles with SupplyMover's cutting-edge features.

The Pharmacist's Companion Series combines everything you need to practice pharmacy consulting and pharmaceutical care in one simple-to-learn, user-friendly, time-saving software package. No more writing notes, sorting through old records to find the outcome documentation, or carrying around reference books. Pharmacist's Companion Series combines everything you need, from nursing home consulting, board, care homes, and hospital patients to individual pharmaceutical care consultant. The Pharmacist's Companion Series was developed for consultants pharmacists by consultants pharmacists. We know how to simplify and organize your job. All of your facility and patient records can be stored in one place for easy access. You can import and export patient and facility information to other programs that you use every day. Transfer patient and facility information from one Pharmacist's Companion user to another.

The best pharma software in Pakistan, with a mobile app for online order management. Pharma Suite is a stable, error-free and affordable solution that handles every aspect of your pharmaceutical distribution business, including batch-wise inventories, recoveries and finance, mobile-based orders, routine supplies and more. This popular pharma software runs at more than 400 businesses in the United States. This pharma accounting software will streamline recoveries, bank accounts, expenses, and cash. You'll also be able to see financial statements. Manage purchases, inventories with costing and purchase returns with ease and maximum accuracy. Integrated recovery management and finance module allows you to manage your customer's and vendor's credit. Invoice efficiently with auto/manual batches, flexible discounts and auto inventory updates, detailed reports, and accurate, error-free batch management.

ATL System's cloud-based software, designed for UK Pharmacy wholesalers and based upon GDP guidelines, gives you access from one central location to stock levels at all your branches. Our goal is to ensure compliance with GDP regulations for our clients. This is achieved by offering a complete solution for managing the wholesale operation of your pharmacy. Our Wholesale Software is based on MHRA best practices. The Wholesale Software was created to give our clients a robust application to prove integrity, auditability and weight of their internal controls to control the movement of pharmaceutical stock. "We take security, control, auditing, and reliable tracking stock to a new level while reducing errors relative to other methods such as excel spreadsheets."

RxMaster Pharmacy System is a pharmacist's system. RxMaster, a fully-featured pharmacy system, is an indispensable part of your team. It helps you work efficiently as well as effectively. Our software provides detailed reports that allow you to monitor important information such as inventory, third-party payment, and other data that can be used for your pharmacy's efficiency and profitability. Innovative and time-saving features will help you keep your pharmacy in good order, ensure compliance, provide excellent customer service, and document your transactions effectively. Many of our features can be customized. Regular system updates ensure that your pharmacy system keeps up with industry changes. We are constantly adding new features to our system and updating as necessary.

Track shipments in real-time, get the best rates, and protect deliveries at risk. All shipments are visible in one place, from start to finish. Monitor and track shipments live, with an exceptions dashboard identifying deliveries at risk of delays. Our professional services protect your shipments through proactive monitoring, targeted interventions, and root-cause analysis to reduce disruption risks. Exportable reports and data analytics protect your relationships with CMOs and specialty Rx partners. They also help you maintain good relations with 3PLs and carriers. Performance trending can optimize costs. Rate comparisons in real-time between national carriers and couriers. API integration and temperature control are available. Protect your pharmaceutical distribution operations. Real-time carrier rate shopping, shipment monitoring and tracking, and professional at risk delivery intervention.

Offer your products to an ever-growing network that includes hospitals, pharmacies and clinics who are looking for a more convenient way to buy products. The traditional wholesale distribution system is expensive for manufacturers, especially small ones. This can affect their pricing competitiveness and profitability. Directly selling to customers is a difficult task and requires resources manufacturers do not have. Smaller distributors have access to drugs in shortage and can offer competitively priced products. However, they struggle to sell to customers who don't want to create accounts or order from multiple suppliers. GraphiteRx provides a modern platform that helps suppliers increase sales to clinics, hospitals, and pharmacies. GraphiteRx is used by over 1K hospitals and pharmacies to manage more than $500M of purchasing outside their primary wholesaler.