Best Pharmaceutical and Biotech Software in Canada

SmartReps allows field sales reps the ability to manage their interactions with healthcare professionals effectively while optimizing their sales performance. The CRM pharma was designed to improve the effectiveness of field reps. SmartReps are designed to meet the operational requirements of medical sales representatives. They also adapt well to your commercial activities. Reps can use CRM pharma data and historical visits to personalize and prepare calls for HCPs, whether online or offline. It's time for your medical, hospital or pharmaceutical representatives to succeed! Smartreps gives field reps the tools they need to engage with HCPs via different channels, resulting in a seamless omnichannel experience. Reps can deliver the most relevant messages to HCPs, whether face-to-face. Smartreps allows field reps to collect and capture all relevant information from HCPs.

SmartTeam allows sales and operation managers to monitor team performance. Transform your data into actionable insight and implement data-driven strategies! The entire software suite was built with life sciences managers in mind. Manage your sales and distributor channels effectively to improve the performance of your sales teams and business results. SmartTeam provides managers with a flexible and comprehensive administration interface that allows them to monitor business conditions, product and delivery information. SmartTeam gives your sales and operations managers access to real-time data from the field. Profit from a powerful Business Intelligence Tool that allows you track all relevant KPIs to your commercial performance. Euris solutions allow sales and operations managers to quickly create, update and share e-learning material. E-learning can help medical representatives meet market needs by synchronizing it with product launches.

Titanium's comprehensive suite of applications is designed to keep your sample-management program compliant, efficient and streamlined in today's ever changing regulatory landscape. Our cloud-based SaaS platform offers unparalleled benefits that are tailored to comply with PDMA, 21 CFR Part 11, and other regulatory requirements. Titanium is a dynamic suite designed to address specific challenges in compliance while seamlessly interoperating. It provides an integrated and comprehensive solution that meets all your compliance requirements. Titanium is designed to grow with your company, ensuring each data point is only stored once and accessible across all applications. Integral audit trails provide transparency and accountability through seamless tracking and reporting. Titanium is a mature application that evolves regularly through upgrades. This keeps you at the forefront in compliance technology.

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.

AI-powered drug discovery is a proven technology. Cerella extracts hidden insights from your drug discovery data to reveal the best compounds and most valuable experiment for your project. It can make confident predictions by accurately filling in the missing values. This is especially useful for expensive downstream experiments, which are impossible to predict using other methods. This allows you to do more with sparse and limited data sets.

Accuracy, speed, confidence. Introduce generative AI in commercial biopharma. Simplify the laborious process of collecting, organizing and inspecting vast quantities of complex data. You can always rely on 100% accuracy to get the insights you need. You'll never again lose track of your workflows with our AI-powered data verification and manipulation platform. All in one place, you can gather, refine and check all your data. Search public and private databases based on key drug characteristics. Segment drugs and clinical trials based on detailed patient profiles. You can extract the data in plain English. Link your answers to their original source. Spend your time and effort on synthesising high-quality outputs rather than sifting through data. Our LLMs allow researchers to scan assets 4.8x faster by hand. We index more than 38M scientific publications and abstracts from conferences, clinical trials, and other sources. All the data that you need, at the time you need it.

Engage healthcare stakeholders in order to gain insights, advance research and share online knowledge. ExtendMed can help you maximize the frequency and quality of your interactions for a fraction of the cost. Let us help you increase your reach and impact. Health Expert Connect is a platform that provides scientific, marketing, educational, and training solutions to pharmaceutical companies, agencies, associations, and other organizations. - Hosting virtual advisory boards - Speaker bureau management: contracting, training, logistics, closeout, Sunshine reporting - Smartphone event engagement: sign-in, slides, polling, surveys, assessments, follow-up - Online product theatres and satellite symposiums

CBO ERP Ltd. is a leading provider for customized software solutions that are process-driven. Their flagship offering is an innovative 6-in-1 customizable ERP system for the pharmaceutical industry that allows businesses to manage and control key aspects, such as manufacturing, distribution and finance, while also allowing mobile and tablet access and online payroll. This ERP system can be used both online and off-line, giving you total control no matter what. Making a mistake in the pharmaceutical industry is not an option. Your customers depend on your products to ensure their health, and a mistake can be fatal. A natural instability of the market has caused nearly all companies to look for ways to streamline their financial services, and adopt improved financial model. Ecommerce is the act of buying and selling products, services, or goods over the Internet. Ecommerce is also called electronic commerce or Internet commerce.

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.

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.

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.