Best On-Premise Pharmaceutical and Biotech Software of 2024

DF mSafety AI, a cloud-based platform, uses AI/ML and automation for a great user interface and efficiency in Safety Case Management, Neutraceutical, Vaccines and Medical Devices. DF mSafety AI was built on Datafoundry’s Integrated Cloud Platform – DF Safety 4.0, which supports scalable, secure AI/ML-driven Safety Case and Signal Management. It also includes pre-built connectors for enterprise systems and adheres to industry standards and regulatory requirements.

Platforce CRM, a cloud-based CRM that automates industry-specific business processes and improves customer engagement, is a closed-loop marketing and customer relationship management solution for pharmaceutical and life sciences companies. The system allows you to manage all aspects of marketing and sales activities, from the marketing cycle creation through territories assignment, databases creation, calls carrying, and KPI analysis.

Select the best experts who are the most qualified in the areas that you want to achieve. With Kolexia, you can optimize your recruitment strategy of KOLs* according to your objectives. This is done through an intuitive interface that allows for precise digital and scientific qualification. Kolexia's database is unique, combining information about health experts and their work. This wealth of information allows for a more in-depth analysis on their profiles, their collaborations and their impact within their field of expertise. This approach allows us to provide a comprehensive, up-to date view from opinion leaders in order to optimize medical strategy. *KOL: Key Opinion Leader

Enterprise Quality Management Software in cloud for life sciences. Technology plays a crucial role in ensuring that QA is aware of any issues as they arise in today's complex operational environment. You can gain insight into your quality management system's performance and the current state in your operation to be more proactive and reduce risk. Montrium's Enterprise Quality Management system (EQMS), was designed to help life science companies tackle the content management challenges they face head-on. Each module of the SharePoint QMS can be used separately or as part of a fully integrated quality management platform. These modules can be used on-premise or in a cloud environment. These modules are ideal for pharmaceutical companies, contract manufacturers, and medical device companies. Built to comply with GMP/GCP requirements.

Nextflow Tower is an intuitive, centralized command post that facilitates large-scale collaborative data analysis. Tower makes it easy to launch, manage, monitor, and monitor scalable Nextflow data analysis and compute environments both on-premises and on the cloud. Researchers can concentrate on the science that is important and not worry about infrastructure engineering. With predictable, auditable pipeline execution, compliance is made easier. You can also reproduce results with specific data sets or pipeline versions on-demand. Nextflow Tower was developed and supported by Seqera Labs. They are the maintainers and creators of the open-source Nextflow project. Users get high-quality support straight from the source. Tower integrates Nextflow with third-party frameworks, which is a significant advantage. It can help users take advantage of Nextflow's full range of capabilities.

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.

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.

AmpleLogic EDMS Software, a powerful electronic document management system, is designed exclusively for Pharmaceutical and Biotech Companies. It was developed and implemented to meet the cGMP requirements of Pharma domain, with 21CFR Part 11 Compliance, EU Annex 11 Compliance, which can easily eliminate the challenges faced by various companies. AmpleLogic EDMS, a paperless system for document management, allows you to manage all documents and information with ease. AmpleLogic Document management system includes a variety of activities such as document creation, review and approval, editing, document comparisons, version control and parallel reviews.

AmpleLogic's Quality Management Software is designed to meet the strict requirements of industries that are heavily regulated. The ISO 9001-certified cloud-based Quality Management System is ideal for Lifesciences and other industries such as Food & Beverages, Cosmetics, Medical Devices or Gene Therapy. Businesses are adopting QMS solutions as they recognize the challenges of manual quality checks, which can be laborious and prone to errors. These systems are crucial in improving audit quality by automating processes, managing data efficiently, and integrating APIs.