LifeSphere RIMS Alternatives

With the ever-increasing complexity of global medical device registration regulations, more companies are turning to regulatory information management systems software (RIMS software) to streamline the application life cycle and manage medical device applications. RegDesk is the most comprehensive AI-enabled RIMS platform for Medical Devices, Pharmaceuticals, and IVD companies offering enhanced performance and positive results more consistently than any standard regulatory information management solution. Our capabilities are as follows: • AI Application Builder • Regulatory Intelligence • Change Assessment • Standards Management • Country-Specific Templates • Distributor Collaboration • AI Document Management • Tracking & Reporting • Alerts and Notification • Product Management • Claims Management • EUDAMED For more information, visit our website.

ACE is a quality management software solution for companies of any size, in any stage, in any highly regulated industry. ACE is fully configurable allowing your company to adapt ACE to fit into your exact quality needs. 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. 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! 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.

Bringing breakthrough products to market in highly regulated industries can feel like an endless series of trade-offs. MasterControl's software simplifies GxP workflows so you never have to sacrifice quality for cost or innovation for regulation. Complete and connected meets fast and flexible. From quality event management to document control and integrated training - MasterControl Quality Excellence transforms your quality data and processes into a competitive advantage. Modernizing your manufacturing operations starts with modern software. From work orders to work instructions and production records (EBR or eDHR) to logbooks, MasterControl Manufacturing Excellence is the simplest way to digitalize manufacturing.

DF mSafety AI is a cloud-based safety platform that uses the power of AI/ML and automation to deliver efficiencies and a great user experience in Safety Case Management and Signal Detection for Drugs, Cosmetics, Vaccines, Neutraceutical and Medical Devices. DF mSafety AI is built on Datafoundry’s Integrated Cloud Platform - DF Safety 4.0 which supports scalable and secure AI/ML driven Safety Case and Signal Management, pre-built connectors to enterprise systems, adhere to regulatory requirements and industry standards.

Essenvia drives business value and brings cross-functional efficiency gains to all teams and departments. Centralized repository for all regulatory information, enabling collaborative authoring and reporting while eliminating technical holds, RTAs, and RFIs. Empowerment of regulatory affairs department to accelerate product launches and eliminate revenue loss due to submission delays and missed renewals. Helicopter view of the total regulatory lifecycle. Executive dashboards, metrics, and proactive alerts for global registrations, submissions, and change assessment. Essenvia is a RIM Platform that enables you to manage regulatory workflows across the total product lifecycle, accelerate global market access, and generate exponential business value. Consolidate your regulatory activities into one centralized platform and bring your devices to market faster. Central repository for all registration docs linked to product master data. Manage product registration lifecycle by country.

Rimsys is bringing regulatory order to the medtech industry. The Rimsys Regulatory Information Management (RIM) platform digitizes and automates regulatory activities, freeing teams from inefficient administrative work, and helping them confidently establish and secure global regulatory compliance. Unlike complex, color-coded spreadsheets, or expensive external consultants, Rimsys seamlessly centralizes all regulatory information, automates submission processes, and monitors relevant expirations, standards, and global regulations. Traditional approaches to regulatory affairs can’t keep pace with the growing complexity of the global landscape, and overburdened teams face increasing compliance risks. Rimsys streamlines all regulatory activities including registrations, essential principles, UDI, standards management, and regulatory intelligence in a single, integrated platform.

RegDocs Connect gives your operational and regulatory teams the tools they need to prepare complete and compliant submission ready documents and records. Built with the end user in mind, collaboration, automation and quality are the foundation of this solution. Automated workflows manage your records lifecycle from draft to final, enabling your team to be in complete control of your regulatory documents at all times. Mapping of document types to the EDM reference model and eCTD facilitates organization and retrieval of documents for inclusion in regulatory submissions. Proprietary tools such as PDF/A Publishing, document classification, and unique document identifiers provide a powerful regulatory document management solution that pulls information from across your organization, into one manageable solution. With the rise of electronic submissions to regulatory agencies and the increased complexity of drug development, the ability to produce submission-ready, quality content

End-to-end regulatory information management on a single platform. The Vault RIM Suite streamlines global regulatory processes on a single, cloud-based platform, enabling life sciences companies to improve visibility, data quality, and agility. Respond faster to changing regulations and increase process efficiency from submission planning to publishing. Coordinate regulatory efforts across HQ, affiliates, and partners within a single RIM system. Ensure teams are developing reliable regulatory content with high data integrity. Veeva Vault Registrations manages product registration data worldwide, including registration status, variations, and health authority interactions. Veeva’s flexible data model accommodates IDMP data points and will continue to support evolving regulatory data standards. Veeva Vault Submissions streamlines submission planning through approval by automating regulatory process steps.

Kalypso provides life sciences companies with a cost-effective accelerator for a RIM system implementation - Accel for RIM. The solution enables an integrated platform to effectively manage and track product registrations, accelerate and improve the submissions accuracy, manage global UDI information, and enable efficient product distribution. It consolidates compliance and quality data from various enterprise solutions into a global source of truth for product registrations and tracking to accelerate regulatory submissions. Deployed using modern APIs to aggregate product data, regulatory documentation and submission packages. Pre-configured for rapid implementation with a validated software system. Based on industry-leading RIM practices and implementations.

Imagine all of your regulatory information regarding products, registrations, submissions, correspondence and commitments in one centralized place accessible from anywhere. With Ennov RIM, life sciences companies can streamline their regulatory processes, improve their data quality, quickly answer business-critical questions and effectively respond to health authority requests. Ennov RIM is a purpose-built application (based on Ennov Process) for the management and tracking of therapeutic product details and registration information. Whether you are planning the launch of a new product or handling variations to existing registrations, Ennov RIM provides Regulatory personnel with the key information and functionality to effectively manage your product portfolios worldwide.

All-in-one global regulatory affairs system, complete with registration management software and worldwide assistance from regulatory experts. The registration system you need to initiate, renew, amend or transfer your medical device or IVD market access approval. LICENSALE®‘s intuitive user interface with real-time data includes complete project management, infographic analytics, an effective collaboration platform, future market access planning and advanced reporting. It puts you in control of your global medtech registration activities. Arazy Group “in-country” regulatory experts review your compliance documents, assisting in the preparation and submission of your applications. They work with authorities until you obtain your desired marketing approvals. LICENSALE® includes submission and compliance requirements specific for your product in over 140 countries as well as regulatory experts to assist with each of these markets.

RIMExpert™ addresses regulatory planning, tracking and data management by managing the global rollout plans and automating the creation of regulatory applications, activities and medicinal products, RIMExpert™ reduces data entry needs, improving data quality and increasing global oversight and control. Standardize regulatory planning, tracking and registration management processes. Strengthen collaboration between headquarter(s) and affiliates. Create one common place to work in all registration activities. Having one access point to all activities, questions, commitments, correspondence and authorizations for every application. Synchronize efforts for maximum efficiency of enterprise regulatory resources. Control registration activities throughout the lifecycle of the product keeping abreast of timelines and status of commitments and agency questions. Interactive dashboards for actionable regulatory activities and registrations overview.

DXC RIM platform manages regulatory affairs content, data, and workflows in one central location, helping teams accelerate innovation and reduce time to market. The sensitive nature of regulatory affairs (RA) content demands a unified platform to handle regulatory data and workflows. Teams need simple, always-ready access to all relevant data. They also require an intuitive, customizable user interface that is easy to navigate. Collaborative tools and configurable reporting are crucial for success, but legacy technology can frustrate teams and slow processes. Achieving compliance is a struggle. Collecting data and documenting processes is time-consuming. Problems are compounded when life sciences organizations run fragmented legacy systems using disparate technologies. In some cases, they need to resort to spreadsheets to manage key operational processes. Bringing products to market and managing RA requires a centralized, enterprise-grade solution.

Samarind RMS provides a smarter way to manage your medical product information. Using Samarind RMS, you only need to enter data once and can reuse it as many times as required. For example an ‘INN’ can be entered once and reused for all related IMA submissions, renewals, variations, PSURs and XEVMPD submissions. This concept applies to all key data held within the system and is proven to streamline workflows and help to increase data quality. 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) with version control, template creation and the ability to link to external document management systems such as Documentum™ or SharePoint™.

PhlexRIM will dramatically improve compliance with efficient and effective real-time access to your global registration information. PhlexRIM 2.0 contains a library of pre-configured automation assistants, or “bots,” as well as built-in regulatory use cases based on industry best practices. Utilizing an intuitive drag-and-drop design tool, regulatory teams can automate their business processes without programming knowledge or IT support. Manage the lifecycle of pharmaceutical product registration activities. Get extensive status information and use the alert management which is included in all workflows. Illustrate reports using standard reports or design your own reports. Create and assign regulatory tasks across your organization – for management, departments, headquarters, and affiliates.

ViSU™ is a cloud based End-to- End Regulatory Information Management (RIM) platform designed specifically for the medical device industry enabling global users to access and manage Regulatory Data (Product Master, Registrations, Tracking), Dossiers/Tech Files (Submission planning, building & life cycle), HA/NB correspondence, Obligations tracking, UDI, eIFU, Reg Requirements DB and Change Control. ViSU helps you embrace digitization in regulatory that delivers connectivity, traceability and automation leading to regulatory management efficiency, less compliance risks & cost reduction.

Unlock new revenue opportunities through reliable and real-time data and predictive insights. Controlant’s platform delivers actionable insights into your supply chain performance and automates your workflows and processes. Continuous transparency, traceability, and insights for the entire supply chain, from your desktop or mobile. A simple, efficient source of supply chain truth. No gateways or manual USB upload is needed. You own your data. View and report on chain of custody for audits and regulatory compliance. Ensure your products maintain their integrity through the last mile. Reduce product and operational waste by streamlining processes. Leverage smart analytics to achieve measurable ROI. Leverage data analytics to identify and mitigate risk through process improvements. Identify and implement initiatives to reduce waste and your carbon footprint. An intelligent cloud software platform delivers mission-critical supply chain insights and predictive analytics on-demand.

We’re accelerating innovative solutions created to benefit all stakeholders in healthcare, to help increase speed to therapy, reduce prescription abandonment and support improved health outcomes for the patient. We’re committed to removing access barriers to healthcare — whether it’s resolving prior authorization requests or raising awareness around support services. Healthcare is seemingly more expensive than ever. Assist your patients in getting their prescribed therapy with affordability solutions that help with high-deductible health plans, increasing copays and a lack of visibility. For some, staying on therapy can be the hardest part of their healthcare journey — whether it’s learning how to take their medications or simply remembering to do it at the prescribed time. Which is why these adherence challenges must be met with people-first solutions.

Streamline your regulatory processes with our new, end-to-end regulatory information management system, IQVIA RIM Smart. Free your team from labor-intensive maintenance to focus on delivering valuable products to market. RIM Smart is the modern regulatory information management solution built to increase speed, collaboration, efficiency and visibility across your entire global portfolio, improving performance at a lower cost. Delivered securely in the cloud, IQVIA RIM Smart provides interconnected, comprehensive and intelligent management of the entire regulatory process. IQVIA safety and quality platform integration will heighten performance and enhance flexibility. Automate manual processes and increase connectivity for improved efficiency, cost savings, and better coordination and cross-enterprise visibility.

PharmAssist is a robust Distribution Management solution for managing all needs of wholesale & Distribution businesses providing you an edge over others. It has a user-friendly interface and helps organize all business activities including orders, delivery, and collection- tracking making it a seamless flow. It offers the added advantage of fast billing, and organized & scientific stock arrangement, which helps in faster stock removal & delivery. To streamline, automate & optimize the workflow of our clients, primarily in the pharmaceutical & healthcare sectors, by using a proactive & collaborative approach. As our prime focus is to help pharmaceutical companies manage the logistics of their distribution & retail operations. This includes tracking the entire sales life cycle of pharmaceutical products – beginning from the manufacturer through the distributor and retailer & finally ending with the customer.

Regulatory functions hinge on high-cost contributors across a variety of regulatory content. A cloud-based offering like Infosys regulated document management platform is the perfect solution to this problem. Externalization, collaborative authoring and editing. Simplify governance, processes, and implement consumption-based commercial model; provide support for audit trails. Create custom workflows, and provide support for versioning; implement a proven solution with 99.95% guaranteed uptime in production. Our solution enabled business users to search documents from a vast repository within 3/4 seconds. The new system also offered users unlimited on-demand storage. The DMS uses Google application programming interfaces (APIs) to reduce operational and maintenance costs. The company’s overheads are limited to API usage and storage space.

Keep all your documents and drawings in one place with our top-performing enterprise document management software. Meridian provides a single source of truth, configurable workflows to streamline collaboration with all internal departments and ensures every document change is versioned and audited to demonstrate regulatory compliance. Engineering document management is the process of effectively searching for, finding and managing the complex engineering documents – including CAD files, drawings, designs, technical documents and communication documents, that exist in AEC organizations (Architecture, Engineering & Construction). Effective engineering document management can often be difficult for businesses in these industries. Meridian’s document management system for engineering projects can resolve these concerns. Meridian can centralize an organization’s relevant documents and drawings while automating key processes.

With ever-changing national regulations, data standards, and complexities around preparing for regulatory submissions, regulatory affairs organizations in the healthcare and life sciences industry are convinced and driven towards smarter processes and intelligent systems to optimize costs, maximize accuracy and minimize timelines for the submission. Addressing the concern, regulatory information management, RIMTrack, is a cloud-ready artificial intelligence (AI) based new age regulatory information management system. It’s developed from scratch with the mission to help organizations to prepare submissions accurately and efficiently and by streamlining the regulatory processes related to tracking, licensing, approvals, regulatory and competitive intelligence, clinical trials, and reporting across global sites and stakeholders. Integrate with existing RIM system and achieve complete end-to-end management of regulatory life cycle process.

ClinChoice manages global regulatory information with expert technology prowess, a deep understanding of global and local regulations, and the best data management practices. ClinChoice applies its expertise in regulatory affairs and technology to help organizations manage their regulatory data. Our consultants provide general data maintenance support in regulatory information management system (RIMS) software to deliver solutions that will ensure application submission, approval, renewals on time, improve operational process efficiency and tracking. We provide the required support in the management and control of the drug registration process, which helps the drug and medical device manufacturing companies to have visibility and tracking of all regulatory information. With our help, organizations can develop short- and long-term strategies to meet submission timelines with minimal impact on day-to-day operations.

Drive study efficiency, regulatory compliance, and patient safety with Alpha Clinical Systems' electronic drug inventory management system (DIMS). Reduce site errors and workload while gaining real-time transparency. A comprehensive web-based system, ez-DIMS streamlines drug and device distributions at the site to eliminate transcription errors. Integrated with ex-SourceDocx, automatically accounts for supply disbursements, providing real-time visibility of drug inventory. Replace slow, error-prone, manual processes with user-friendly ez-DIMS. Reduce site workload with user-friendly scanners to quickly, easily, and accurately record study supply inventory and accountability at the patient, site, and study levels. Drug inventory violations at the site are the second most common regulatory inspection finding. Reduce medication assignment/dispensation errors by leveraging QC cross-checks between ez-DIMS and ez-SourceDocx.

We understand that every click is an opportunity for error. Formweb minimizes patient risk by combining everything your physicians need to quickly and safely prescribe medication into one user-friendly site at the point of care. With other pharmacy formulary tools, these resources are difficult, if not impossible, to find in time to treat your patient. Does your formulary software save patient lives? Formweb exists not only to satisfy regulatory requirements but also to save your patients’ lives and your hospital time and money. As the formulary experts, we simplify the search process, saving time, decreasing calls to the pharmacy, assisting with hospital compliance, and most importantly, reducing risk and improving quality of care.

Everything you need to successfully register your medical device or IVD product in any market around the world and manage your market access license through the product life cycle. REGISLATE® provides users with medical and IVD device-specific at country-specific complete submission file requirements. Users can manage milestones, timelines and estimated and actual completion dates for initial registrations, renewals, amendments and license transfers in real-time. Infographic data and proprietary indicators for clear monitoring and management of each project are available. Utilize collaboration tools for preparation and review of submissions, compliance requirements and documents. Recieve progress reports in real-time for current and future submissions including market access readiness index. REGISLATE® includes GR-MAP registration tracking for both country and product.

GHX Exchange Enterprise modernizes the healthcare supply chain through increased standardization and automation. Traditionally, providers have managed the order cycle and their growing teams manually, which can increase error rates and impact performance. GHX Exchange Enterprise digitizes the entire cycle for more efficient processes, more connected supply chain data and better performance insights. GHX provides healthcare organizations with a more complete picture of their supply chain—and how it’s delivering on business goals and objectives. GHX Exchange Enterprise automates transactions to help reduce data entry errors and administrative costs. This in turn helps generate more accurate data for supply chain improvements and decision making. From order to invoice, GHX Exchange Enterprise helps you better manage processes, increases data accuracy and quality, and improves overall performance.

AmpleLogic Regulatory Information Tracker is built on the LOW CODE AND NO CODE (LCNC) PLATFORM and comprises two modules: ANDA and DMF Tracker. This Pharmaceutical RIMS Software can help you improve the quality of your data, boost operational efficiency, decrease mistakes, and streamline communication across departments.

OpenText™ Information Management solutions help life sciences organizations leverage insights from data and content to improve decision-making processes and accelerate product development. Integrate, manage, and securely exchange data across people, systems and things. Leverage information assets from R&D to commercialization. Freedom of choice with cloud-native software that can run anywhere. OpenText for life sciences accelerates the discovery process by extracting actionable insights that drive pipeline innovation. Capture and manage research papers into electronic lab notebooks with intelligent capture. Find insights with text mining. Extract knowledge trapped in the unstructured text contained in clinical trial reports, study protocols, clinical safety and efficiency findings. Find out how to intelligently analyze, classify and extract clinical trial documents to reduce the risk of costly stops and starts.

At Calyx, we know that the success of your clinical development program comes down to data. Which makes the effectiveness of your electronic data collection (EDC) system key. Used in over 2,600 worldwide clinical trials, Calyx EDC streamlines clinical trial data collection and reporting—in one easy-to-use platform. Don’t trust your important data to just anyone. Contact us to learn how Calyx can propel your program’s success. Calyx EDC gives you the flexibility to easily plan, design, and conduct studies, regardless of their complexity. With features that help reduce costs, improve site visibility, and drive efficiency, Calyx EDC keeps your trial on track.

Our flagship products include Speed Script PRM, an all-inclusive pharmacy management system, Speed Script POS, an integrated point-of-sale system for managing your front-end sales and Speed Script LTC (SSLTC), an electronic facility to pharmacy communication application - fully equipped with drug pass and eMAR technology for long-term care providers. For more than 40 years our defining attribute has been, and still remains, our dedication to sensational customer service. Speed Script PRM, is built with today’s independent pharmacy in mind. Integrating features like Text Messaging, electronic document storage and management, wireless signature capture, mobile delivery app, accounts receivable/in-house charge accounts, custom reporting, and many other features built directly into the speed script prm system.

Today’s pharmacies face many challenges, from managing an increasingly wide breadth of products to managing drug shortages and ensuring consistent vendor and DSCSA compliance. The pharmacy purchasing and inventory management software solutions from SureCost are here to save you time and money so that you can navigate those complexities successfully. SureCost is the smarter purchasing solution and our pharmacy customers typically save 2-5%+ on their cost of goods year over year. Bring your entire catalog into one seamless solution, saving your pharmacy thousands of hours and thousands of dollars every year. SureCost’s purchasing, inventory, and compliance management solutions empower you to unify purchasing and inventory, work smarter, and maintain vendor and DSCSA compliance. SureCost unifies pharmacy purchasing and inventory, so you can optimize your buying decisions and discover money-saving opportunities using your entire vendor and wholesaler catalog.

Saveo is the one-stop solution for all your pharmacy needs. Saveo is a B2B managed marketplace for pharmacies, bringing primary & secondary medicine markets together, offering faster delivery, cheaper procurement & better technology to pharmacies. It runs with an aim that no prescription shall bounce in India. Indian pharmaceutical industry is highly fragmented with 6.5lakh retailers and 65000 distributors, unlike the US where there are just 5 major distributors covering 93% of the market share. We aim to streamline this supply chain by being a single distribution point and empower these 6.5lakh micro-entrepreneurs with technology and sustainability. Saveo runs on a mission to empower traditional pharmacies by building a reliable, scalable, and efficient healthcare supply chain.

UNISOLVE is a premier software solution for pharmaceutical wholesale and distribution businesses. The software streamlines business operations by offering digital solutions for billing, stock auditing, product inflow, stock selection, online order taking, delivery optimization, real-time reporting, and decision-making. The software reduces the operating costs involved in inventory management, product delivery, and other organizational operations. Pharmaceutical Wholesale and Distribution businesses can use UNISOLVE software to run their businesses with minimal resources. It is a 100% accurate and dependable solution for all their needs.

MedEx is a suite of solutions that control, secure, and track the preparation and distribution of medications and supplies. As the most comprehensive hospital workflow management solution on the market, we improve the compliance, efficiency, and safety of preparation through 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 all medications included and alerts your staff to missing, misplaced, recalled, or expired items, helping guide and speed proper replenishment for a safe configuration. Your staff will save time; patients will be better protected; and you’ll receive the metrics you need to optimize both your tray and inventory management. Choice of processing using a stationed kiosk or mobile device. Visual confirmation of medication placement using 2D versus expensive RFID tags.

Antares Vision Group has developed a digital healthcare solution for automating drug and medical device logistics, which eliminates or reduces activities that do not generate value for the patient while introducing a new paradigm of process efficiency for healthcare providers. The Medication Management Platform eliminates non-value-added activities that can help hospital systems optimize the time of medical and nursing resources to focus on patient and patient safety. The Medication Management Platform allows the complete traceability of the flow of medicines and medical devices, combined with automation systems that can help improve efficiency and operational excellence within healthcare institutions. The combination of automation systems and traceability allows for the better management of reorders and stocks, both at the central and peripheral levels, avoiding the waste of materials due to expiration.

BeeCTD is a full-featured eCTD management solution for pharmaceutical companies and regulatory agencies. Modular architecture and transparent licensing policy allow our users to choose from modules which they want to use – Reader, Compiler, Validator. Full-featured Reader which helps you to get an overview of the entire lifecycle of the dossier containing eCTD and/or NeeS sequences, including baseline submissions while transferring from NeeS to eCTD. Realtime, fast sequence validator fully compliant with eCTD / NeeS technical specification, incl. best practices criteria. The latest version of eCTD validation criteria is always updated, older versions are available. Get your documents compiled into the eCTD-compliant format. Use our eCTD compiler tool as a product, which allows you to compile yourself or as a service - we compile for you on demand.

Delivery services are no longer “nice to haves.” Your patients expect the option of having their medications delivered to their homes, and pharmacists are happy to comply. However, medication deliveries require a few extra steps. The PrimeDELIVERY solution offers secure, on-time medication deliveries that meet all regulatory requirements. Best of all, records flow seamlessly back to the PrimeRx operating system. All prescriptions set for delivery are marked as “out for delivery” in the pharmacy’s system. Once the delivery is actually made, that notation is changed to “delivered.” If a prescription needs to be returned to the pharmacy, the patient record will automatically be updated. Undelivered medications are returned to inventory, with stock levels automatically adjusted. The system generates an advance electronic signature request to the patient ahead of a scheduled delivery. The patient provides a signature, which is transmitted back to the pharmacy via PrimeDELIVERY.

Analysis of prescribing physicians based on your market, specialty, region and healthcare coverage. Identification of physicians that were visited or not. Access to the prescription record of each professional within the “filters” created by the Rep’s. View the physician file and quickly recognize physicians’ prescription profile. Access an automated and quality integration solution ready to be used. Platform with multi-device design, it may be used in Smartphones, tablets, iPads and computers.

Know how to distribute your product in pharmacies and optimize their sales performance in the market. Segmentation of pharmacies according to your specific market. Evaluation of the quality of the distribution of your product in pharmacies. Evaluation of coverage in a numerical and weighted form. Mapping of additional sales opportunities for your product as from an enhanced distribution. Definition of a commercial strategy to leverage the sales of your product. Orientation and sizing of your commercial team. Pharmacy distribution diagnosis helps define distribution targeting and product placement targeting. Ideal for the launch and maturity stages.

SupplyMover is the only CRM, e-commerce, and sales enablement suite built specifically for distributors. Manage and organize all of your operations in one, intuitive platform and gain access to a suite of best-in-class tools built with unique industry processes in mind. SupplyMover gives you everything you need to see, understand, and organize your data in seconds. Get AI-powered suggested selling recommendations, an online shopping portal, customer and product management, analytics, workflow automations, automated lead management, and more. Design and build the perfect workspace for every distribution industry and role with SupplyMover’s cutting-edge features.

The best pharma distribution software in Pakistan with an online order management mobile app. Pharma Suite is the most stable, error-free, and affordable solution for pharmaceutical distribution businesses that handle every aspect of your business including batch-wise inventory, recoveries, finance, mobile-based ordering, routine supplies, and much more. This popular pharma software is running at more than 400 businesses across the country. Streamline recoveries, cash, banks, and expenses, and get ready to see financial statements with this pharma accounting software. Manage purchases, inventory with costing, and purchase returns with easy and optimum accuracy. Manage your customer and vendor's credit with integrated recovery management and finance modules. Efficient invoicing with auto/manual batch invoicing, flexible discounts, and auto inventory updates with detailed reports.​ Accurate, error-free batch inventory management with automatic updates synced to invoicing.

The RxMaster Pharmacy System thinks like a pharmacist. As an innovative and fully featured pharmacy system, RxMaster is an indispensable member of your team that helps you work efficiently and effectively. Detailed reports from our software helps you keep tabs on important information including inventory, third-party payments, and many other key pieces of data that can be used to keep your pharmacy both efficient and profitable. Innovative, time-saving features help you keep your pharmacy running smoothly, maintain compliance, document effectively, and give your customers the best service possible. Many of our features are also customizable. Regular system updates make sure that your pharmacy system is keeping up with the changes and demands of the industry. Along with these necessary updates, we are always adding new features and improvements.

Pharmacist's Companion Series brings it all together--everything you need to practice consulting pharmacy and pharmaceutical care in one easy-to-learn, easy-to-use, time-saving software package. No more written notes, sorting through old records for outcome documentation, and carrying along with reference books. From nursing home consulting, board and care homes, and hospital inpatients to individual pharmaceutical care consultants, Pharmacist's Companion Series brings it all together, all in one place. Pharmacist's Companion Series was created for consultant pharmacists by consultant pharmacists, so we know what it takes to organize and simplify your job. Store all of your patient and facility records in one place for quick convenience. Import and Export patient and facility information to and from other programs you use every day. Transfer patient and facility information to other Pharmacist's Companion users.

Get the best rates from carriers and couriers, track shipments in real time, and protect at-risk deliveries. End-to-end visibility into all shipments through all carriers, presented in a single pane of glass. Monitor and track shipments in real-time, supported by an exceptions dashboard that identifies deliveries at risk for delays. Our in-house professional services safeguard your shipments with proactive monitoring, targeted intervention, and root cause analysis to reduce disruption risk. Exportable reporting and data analytics help protect your relationships with CMOs, specialty Rx partners, 3PLs, and carriers. Optimize costs with performance trending. Real-time rate shopping among national carriers and couriers, including API integration and temperature control options. Safeguard your pharmaceutical distribution operations. Real-time carrier and courier rate shopping, shipment tracking and monitoring, and professional at-risk delivery intervention.

Designed specifically for UK Pharmacy wholesalers and based on GDP guidelines, ATL System's cloud-based software gives you access to the stock levels at all of your branches from one central location. Our objective is to manage our client’s compliance with GDP regulations. We achieve this by providing a complete solution to manage the wholesale operation of your pharmacy. Our Wholesale Software has been designed based on MHRA best practice requirements. The idea behind the Wholesale Software is to provide a robust application that our clients can utilize to demonstrate integrity, audit ability and evidential weight of their internal controls for the movement of pharmaceutical stock. ‘We take the security, control, auditing and reliable tracking of stock to a new level while reducing the likelihood of errors compared to alternative methods utilized such as excel spreadsheets.’

Offer your products to a fast-growing network of hospitals, pharmacies, and clinics that need a better way to purchase products outside of their primary wholesaler. Manufacturers, especially smaller ones, pay exorbitant fees through traditional wholesale distribution, impacting pricing competitiveness and profitability. However, selling directly to customers to reduce distribution costs is challenging and requires resources that manufacturers lack. Smaller distributors carry competitively priced products and have access to drug shortage items but struggle selling to customers who do not want to set up accounts and order from dozens of separate suppliers. GraphiteRx solves these challenges with a modern marketplace platform that allows suppliers to increase sales to hospitals, pharmacies, and clinics, cost-effectively. Access a rapidly growing number of over 1K hospitals, pharmacies, and clinics that use GraphiteRx to manage over $500M in purchasing outside of their primary wholesaler.

Dow Jones Risk & Compliance is a global provider of best-in-class risk data, web-based software applications and scalable due diligence services that help organizations manage risk and meet regulatory requirements related to financial crime, third-party risk management, sanctions and international trade. Built on the legacy of one of the world’s most trusted newsrooms, Dow Jones Risk & Compliance combines the expertise of a multilingual research team with industry-leading data scientists and technologists to provide actionable content structured specifically for compliance needs. Our solutions were developed in partnership with top legal and political advisors — including former regulators — to help our clients maintain consistency across global business units and teams.

Choose just the solutions you need right now. Later on, you will be able to add more capabilities with no problem. The LORENZ Foundation handles Controlled Vocabularies, Repository Management, Interoperability Management and User Management by centrally streamlining system management as well as maintenance and deployment. Benefit from a network of specialized systems that harmonize with each other. LORENZ solutions work flawlessly with third-party software, giving you the flexibility to choose your perfect fit even outside of the LORENZ portfolio.