Pharmaceutical Software Development Services

Software development for pharma companies can vary greatly in terms of project duration. The average duration of a pharma software project depends on the following factors:

• The number and complexity of user screens and dashboards
• The specific number and quality of technologies involved in the project
• The number of concurrent user connections
• The complexity of pharma application architecture.

…and several other factors. Basically, a small pharma application with a limited number of business features can be developed and tested within 4-6 months. More complex pharmaceutical IT solutions can take 9-12 months or longer. Estimated project duration can be reduced if you start with an MVP strategy.

We are trying to keep the hourly rate we offer per pharma app development project as optimal as possible. At TATEEDA GLOBAL, we employ a range of strategies, including a mixed team of local and remote talent working under our R&D offices in Eastern Europe and other locations (as mentioned above, we do not employ freelancer developers or other tech specialists.) Each project comes with a custom price tag that depends on many factors (like team composition, for example). Please contact us for more information!

We possess a wide and exceptionally diversified toolbox of skills, with everything at hand for your full-cycle pharma software development process: for example, .NET domain technologies for building complex cross-platform solutions for pharma product trade (like online pharmacies) and manufacturing (like large-scale pharma product-distribution platforms). A pharma application can include many different technologies, depending on its structure and design. For example, if your project is web-based, we can employ technologies for front-end and back-end development, including JS, Dart, SQL, HTML in addition to many other associated technologies. We invite you to discuss your project with us in detail so we can offer you a set of individualized solutions perfectly suited to your specific requirements.

TATEEDA offers every single service needed to deliver custom pharmaceutical IT solutions, all built with a deep understanding of industry compliance and safety standards. Each system addresses your individualized operational challenges based on your unique workflows and bottlenecks as determined by your project plan and our tech audits.

HIPAA and CCPA compliance are foundational to our development processes, ensuring that every line of code is not only secure but also hackerproof through advanced security protocols. Our solutions are tailored to fit your exact business needs. Some of the core systems we develop include:

• Drugstore inventory management systems enable pharmacists to track stock levels accurately, prevent overstocking or shortages, and automate reordering processes to ensure the right medications are always on hand.
• Pharmaceutical warehousing solutions designed to improve the organization, tracking, and timely distribution of medications. This includes optimizing storage layouts, managing expiration dates, and integrating with distribution networks to ensure that medications are delivered promptly to pharmacies and healthcare providers.
• Manufacturing process management software, which allows pharmaceutical companies to monitor, automate, and adjust production lines in real-time, improving efficiency, reducing downtime, and ensuring that products meet stringent quality standards.
• Claim processing systems to automate and accelerate health insurance claims for pharmaceutical products, reducing manual workloads and improving accuracy.
• Medication retail and distribution platforms that streamline operations from manufacturer to customer, enabling pharmaceutical companies to handle sales, shipments, and invoicing with ease.
• Online portals for pharmaceutical trade, providing convenient and secure access for pharmacists, distributors, and patients. These portals allow patients to make online payments, process insurance claims, and arrange for the delivery of their prescribed medications.
• Biotech device integration software, which facilitates seamless data transfer between medical hardware devices and central systems, ensuring smooth operations and accurate reporting.

At every stage, we focus on delivering systems that not only address your operational requirements but also safeguard sensitive data, streamline workflows, and ensure full compliance. We’re always ready to provide helpful assistance to ensure that the software we build integrates perfectly with your business ecosystem.

At TATEEDA, we combine hands-on experience with both American and Canadian pharmaceutical companies and a robust network of pre-vetted engineers from nearshore and offshore locations. All of our engineers are direct employees, and we guarantee their reliability and professionalism throughout every stage of development.

In terms of HIPAA compliance, we take data security seriously, signing NDA agreements with everyone involved in the project. This ensures that all IT operations, including DevOps, are meticulously managed to protect your business data, ideas, and intellectual property. Whether we’re optimizing cloud infrastructure or automating workflows, security, and compliance are central to everything we do.

While our competitive rates offer excellent value, we never compromise on quality. We’ve developed a deep expertise in .NET and JavaScript, two key technologies for pharmaceutical web-based solutions. Moreover, we continuously refine our skills to stay ahead in the industry. This includes obtaining certifications, actively participating in IT conferences, and ensuring that our developers have enough rest and time to stay productive and creative.

Our DevOps practices further ensure smooth deployments and provide ongoing support to keep your systems running efficiently and securely as your business grows. Ultimately, we aim to be a trusted partner, delivering consistent results while safeguarding your operations and helping you meet your goals.