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Innowise empowers leading pharma, biotech, and medical firms to implement FDA and HIPAA-compliant pharmaceutical software solutions that drive competitive advantage. Our expert developers leverage cutting-edge technologies, including AI and machine learning, to integrate reliable LIMS, EBR, and QMS systems. We also complement these systems with advanced analytics and reporting capabilities, which enable data-driven decision making and continuous improvement.
Need to reduce R&D costs and improve quality control in drug development?
Our team expertly manages complex migration processes, seamlessly transitioning your software and data to new environments. Whether migrating to the cloud or modernizing your existing infrastructure, we minimize downtime and guarantee data integrity.
By utilizing cloud technologies, our dedicated developers enable pharmaceutical companies to automate manual, repetitive tasks, speed up experiments through simulations, and make data-driven decisions in just minutes.
Innowise expert developers help businesses build cutting-edge pharmacy apps, including those for medication delivery, prescription reminders, and doctor consultations, to improve patient care and streamline operations.
Our experts are dedicated to protecting your sensitive data, intellectual property, and research findings from cyber threats. We implement comprehensive security strategies tailored to your unique requirements to ensure compliance and mitigate risks.
Innowise’s CTO as a service model provides pharmaceutical companies with flexible access to experienced CTOs. They help businesses improve their technology strategy and optimize operations without the cost and commitment of a full-time hire.
To support pharma R&D innovation, Innowise creates highly accurate 3D models of human organs. These detailed models offer invaluable insights for research, testing, and training, thereby accelerating innovation and enhancing patient outcomes.
Innowise produces 3D videos to educate both doctors and patients about the effects of medications on the body. These captivating videos broaden understanding and promote informed decision-making, improving patient care and treatment outcomes.
Innowise offers flexible IT outsourcing models, including turnkey product development, dedicated project teams, and staff augmentation services to refine your existing projects with our expert pharmaceutical software engineers.
We leverage our expertise to develop robust, scalable, and secure software solutions that optimize your research, manufacturing, quality control, and data management, accelerating your time-to-market and sharpening your competitive edge.
Innowise’s team develops advanced software that empowers researchers to analyze complex molecular data and simulate drug interactions, significantly expediting the discovery and testing of new therapeutic agents.
We implement clinical trial management systems (CTMS) that simplify the complex logistics of clinical trials. These solutions help you efficiently manage patient enrollment, scheduling, and data collection, and ensure compliance with all regulatory requirements.
Innowise creates applications that facilitate seamless communication between pharma companies, healthcare providers and patients, incorporate telemedicine functionalities, and support patients in monitoring their health and adhering to prescribed treatment plans.
To help pharmaceutical companies comply with global regulations such as FDA guidelines, our experts create solutions that manage documentation, streamline reporting, and maintain comprehensive audit trails.
We have experience of integrating GMP-compliant laboratory information management systems (LIMS) that facilitate laboratory workflows, automate data collection and analysis, and guarantee data integrity and traceability.
Innowise integrates custom electronic laboratory notebooks (ELNs) to improve lab data management, secure sensitive research data, and foster collaboration. They also integrate with scientific tools, manage inventories, and accelerate research workflows.
Innowise team develops scientific data management systems (SDMS) to accelerate data management, facilitate data capture, integrate diverse sources, automate workflows, and enhance storage and retrieval. These solutions uphold data integrity and seamlessly integrate with lab systems.
We have experience in integrating CRM systems leveraging platforms like Microsoft Dynamics 365, Salesforce, and Odoo. Our team also provides secure data migration services between CRMs, guaranteeing a smooth transition and minimizing downtime.
Our dedicated team creates software that increases transparency and visibility across the pharmaceutical supply chain. These systems help mitigate risks like drug shortages and counterfeiting while improving operational efficiency and reducing costs.
By leveraging blockchain and RFID technologies, we develop electronic batch record (EBR) and traceability systems that enhance patient safety, prevent counterfeit drugs, and enable seamless product tracking throughout the entire supply chain.
Our team integrates ERP systems integrating various processes, including R&D, manufacturing, quality control, sales, and distribution, onto a unified platform. This refines workflows and efficiency, cuts costs, and assures regulatory compliance.
To optimize equipment management and maintain seamless lab operations, we implement tailored laboratory equipment software (LES) solutions that simplify equipment booking, automate maintenance tracking, and rationalize resource allocation.
We integrate or customize electronic health record (EHR) software that seamlessly integrates patient records across various healthcare settings, enabling better data sharing and collaboration among healthcare providers and facilitating informed decision-making.
We create clinical decision support systems (CDSS) to aid in diagnosis, medication selection, and treatment planning. Using clinical databases and advanced algorithms, they recommend drugs and dosages, warn of interactions, and provide guidelines to improve outcomes and reduce errors.
We create systems that automate core operations of pharmacies like inventory management, prescription dispensing, and billing. These improve efficiency, reduce errors, enhance customer service, and allow you to focus on your core activities.
Concerned about supply chain disruptions and counterfeit drugs?
Properly developed and implemented pharmaceutical software can significantly enhance data management by streamlining operations, ensuring data accuracy, and facilitating compliance with regulatory standards as 21 CFR Part 11. By enabling efficient data integration, real-time monitoring, and secure storage, this software ultimately improves decision-making processes, reduces errors, and strengthens productivity in pharmaceutical operations.
To maintain data consistency and accessibility, and foster analytics, we integrate disparate data sources into a centralized data warehouse using APIs and ETL.
Innowise integrates advanced AI and ML algorithms into software to facilitate predictive modeling, pattern recognition, and anomaly detection.
We craft software to meet stringent regulations like 21 CFR Part 11, incorporating features like electronic signatures, audit trails, and data validation.
Our team builds solutions that quickly accommodate more users, processes, and data, ensuring your systems evolve over time and grow seamlessly with your organization.
Our experts implement robust data validation and cleansing processes to maintain high accuracy, reliability, and consistency, reducing errors and improving decision-making.
Innowise creates tailored intuitive dashboards for real-time monitoring and visualization of KPIs, enabling timely decision-making and improved patient care.
Custom pharmaceutical software lowers operational costs by digitizing every business segment, including R&D, clinical trials, commercialization, drug safety, and patient engagement.
Our pharma development services prioritize data integrity, incorporating robust security measures to protect sensitive data from unauthorized access and cyber threats.
Implementing pharma software is a complex process that can greatly enhance your business operations. A well-designed pharmaceutical management solution offers numerous benefits, including automation, scalability, expanded reach, etc.
Pharmaceutical software streamlines processes and reduces the time to market for new drugs, allowing you to stay competitive and meet customer demands more efficiently.
Robust security features safeguard sensitive data and intellectual property, maintain regulatory compliance, and protect against data breaches, thereby securing your business.
Automating workflows saves time, effort, and money by reducing manual labor, minimizing errors, and storing valuable information digitally.
Our developers make pharmaceutical software architecture scalable for your business growth, ensuring feature-rich and high-performance solutions.
Pharma solutions enable you to expand your business globally, reaching a wider audience and making your products or services more accessible.
Advanced software enhances R&D by enabling efficient data analysis, drug interaction simulations, and outcome modeling, leading to faster discoveries and shorter timelines.
Tailored pharma solutions allow pharmaceutical companies to effectively and securely manage complex relationships and data transfers among various stakeholders.
Up-to-date insights into patient outcomes, drug development, sales performance, and other vital metrics empower you to make more informed decisions and optimize your services.
Pharma software seamlessly integrates with existing systems, improving communication across departments, decision-making, knowledge transfer, and organizational cohesion.
At Innowise, we follow a comprehensive and meticulous pharmaceutical software development process to guarantee the success of each project. Our team closely collaborates with clients to understand their unique needs and recommend the most suitable technology stack, aligning it with their budget, timeline, and long-term objectives.
Innowise understands the critical importance of precision, compliance, and innovation in the healthcare industry. Our expert team develops custom software solutions that address these needs, empowering pharmaceutical companies to succeed. We have a proven track record of delivering tailored LIMS, CTMS, and pharmaceutical drug traceability systems. Through close collaboration, our experts ensure software not only meets stringent regulatory standards but also drives operational efficiency, enhances data integrity, and improves patient safety
Account Manager in Healthtech
At Innowise, we adopt CI/CD practices using tools like Jenkins and GitLab CI to quickly identify integration issues and deploy updates frequently. Our commitment to CI/CD reduces time-to-market and decreases production incidents.
Our developers use state-of-the-art tools and technologies, enhancing the quality and performance of our software while significantly reducing development time. This allows us to deliver solutions to our clients more quickly.
Our team holds detailed sessions with all stakeholders to gather comprehensive requirements, so the software meets functional, technical, and regulatory needs. This approach minimizes the risk of costly reworks and guarantees it fulfills its purpose.
Our dedicated QA team meticulously oversees every stage of software development, ensuring rigorous quality benchmarks are consistently met. This approach results in a defect-free product that adheres to the highest industry standards.
Innowise team proactively integrates risk management throughout the software development lifecycle. Our experts identify, analyze, and mitigate potential risks to prevent issues that could compromise quality or derail project timelines.
We employ a comprehensive testing strategy throughout the development process, including unit, integration, system, and user acceptance testing. This approach allows us to identify and resolve issues early, assuring the software’s reliability, functionality, and quality.
We provide comprehensive documentation throughout the entire process, including requirement specifications, design documents, test plans, and user manuals. This practice ensures complete traceability, regulatory compliance, and easier audits and reviews.
Our team trains end-users on effective software use and actively gathers feedback to understand their experiences, usability concerns, and practical challenges. This feedback loop enables us to make iterative improvements based on real-world user experiences.
Innowise employs the top 5% of industry experts to implement top-notch pharmaceutical software solutions. Our extensive experience in the pharmaceutical sector, strict adherence to industry standards, commitment to quality and security, and customer-centric approach result in engineering cutting-edge custom solutions that seamlessly integrate into existing IT ecosystems. We empower companies of all sizes to facilitate operations, enhance R&D efforts, and accelerate time-to-market for new drugs and therapies. We drive success by:
Optimizing workflows to maximize efficiency and minimize costs
Developing custom software that sets your business apart in the market
Harnessing our deep industry knowledge to stay ahead of the curve
17
years in IT
1800+
IT professionals onboard
1100+
projects delivered
Frustrated by slow and costly clinical trials?
We develop software to streamline clinical trials, accelerate timelines, and ensure regulatory compliance.
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The cost of developing pharmaceutical software depends on various factors including the design of the user interface, the complexity of the software, its features, and how well it integrates with other systems. It’s important to consider all these aspects to get an accurate estimate of the overall cost.
Struggling with outdated systems?
Since 2019 we’ve been enjoying the services rendered by Innowise to implement a strategically important project on the modernization of a network of internal IT systems.
The Innowise team is able to implement new features faster than our internal team would be able to. Their communication is effective and solution-oriented. They deliver high-quality results quickly.
We are pleased to recommend Innowise as a reliable IT outsourcing partner and highly appreciate their attention to detail and professionalism
Absolutely. We have a proven track record of delivering impactful solutions for the pharmaceutical industry. We’d be happy to share relevant case studies that align with your interests and project ideas during our initial discussions. You can also explore our portfolio on our website for additional examples.
Having received and processed your request, we will get back to you shortly to detail your project needs and sign an NDA to ensure the confidentiality of information.
After examining requirements, our analysts and developers devise a project proposal with the scope of works, team size, time, and cost estimates.
We arrange a meeting with you to discuss the offer and come to an agreement.
We sign a contract and start working on your project as quickly as possible.
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Innowise Sp. z o.o Ul. Rondo Ignacego Daszyńskiego, 2B-22P, 00-843 Warsaw, Poland
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