Rapid Custom Applications Delivered to Optimize Your GxP Operations
The pathway for pharmaceutical business process transformation is dependent on lean and intuitive software solutions that can easily coexist in a connected digital ecosystem. From our observations, almost every pharma company has one or more of the below process orchestration challenges across the pharma value chain:
Introducing Techsol's Compier Low-code Platform
Techsol has helped companies realize considerable amount of time and cost savings by developing and delivering process-oriented, easy-to-use, and scalable cloud applications by leveraging our proprietary Compier low-code platform.
Compier Low-code Platform – Key Components
The platform has the following ready-to-use built-in components which are validated for immediate deployment. Based on your business needs, all these components can be quickly configured to translate your manual processes into digital workflows.
How We Can Help
From our experience, we have worked with different types of clients who have had varying requirements for a custom application. Therefore, if you have a business need, our team can help right from software requirements gathering to final delivery of the production application for business use.
Your Questions & Our Answers
We have the expertise and experience to develop the following types of applications:
> Pharmaceutical web applications that focus on process digitalization and automation
> Collaboration Portals that pharma companies need for medical affairs and commercialization
> Data Integration & Analytics apps to facilitate information exchange from cross-platforms and insights generation
A typical custom application development, testing and release takes place anywhere between 25 to 30 weeks.
With Compier, we can shorten the app development time to 15 to 20 weeks depending on the scope, volume of requirements, system integrations, reporting needs, etc.
With the use of advanced technology and quality-driven processes, our medical writing team members collaborate with Biostatistics, Medical Affairs, Drug Safety and Clinical Data Management teams to deliver accurate and purposeful publications and other medical content with a quick turnaround with 100% compliance to global regulatory requirements. Every medical writing project is meticulously managed and delivered with stringent scientific, statistical, editorial and quality control review.