Biotechnology and Pharmaceutical Project Management Software
Push Back the Frontier of Health with Fit-for-purpose PPM
Get an enterprise view of all projects, products, programs in order to better select, prioritize and deliverPharmaceutical Project Management Software Through Sciforma
The pharmaceutical industry is unique. You need a granular view of all projects: the materials ordered, the resources working, the project risk, and more.
And yet, some pharmaceutical companies think they can grab a project management software that was designed for social media marketing companies and expect it to work with their business model.
For pharmaceutical project management, you should instead look to Sciforma.
Sciforma was made for pharmaceutical project management.
Features like real-time time tracking, project overviews, and complex resource management showcase the singular capabilities of Sciforma.
We got our start making project management software specifically for biotechnology and pharmaceutical businesses, so we have been in this market for a long time. We’ve seen every potential roadblock and every missing feature, and we’ve been able to grow and adapt to best fit your industry’s needs.
Get an enterprise view of all projects, products, programs in order to better select, prioritize and deliver
50-90%
reduction in project failure
Improve Control Over Capacity to Achieve More
Sciforma’s track record includes a 60 to 80% improvement in resource utilization for pharma clients. Gain perfect resource visibility to get a better handle on project lifecycles and launch more life-saving products60-70%
increase in on-time project delivery rate
Centralize Decision Data and Process to Improve Decision Quality and Consistency
Align all stakeholders, including but not limited to:
- • Project managers
- • Clients
- • Providers
- • Owners
- • Staff
- • Subcontractors
And get everybody on the same page, and headed toward success.
Benefits of Sciforma Healthcare Project Management
Sciforma integrates regulatory compliance tracking, ensuring adherence to stringent guidelines such as FDA requirements.
We also provide robust documentation management capabilities for handling extensive clinical trial data and research documentation securely.
Advanced scheduling tools facilitate precise project timelines and resource allocation, crucial for managing drug development phases effectively.
Additionally, real-time collaboration features enable seamless communication among multidisciplinary teams, including researchers, clinicians, and regulatory experts, fostering efficient decision-making and accelerating time-to-market for new therapies.
Sciforma thus enhances productivity while maintaining compliance and quality standards essential in this highly regulated sector.
If you’re ready to learn more, get in touch with Sciforma. We would love to hear about your project.
Review some of our success stories below.
See what some of our current customers say about us
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