PROCESS & QUALITY DATA CONNECTED
Breaking data silos to increase your operational efficiency.
In a GMP compliant way.
Why we have created Appliant
“We are devoted to digitalizing manufacturing process; empowering our clients to produce more affordable, faster and quality drugs to patients.”
WHAT WE DO
From data integration to predictive quality, Appliant MIP optimizes every stage of the process to achieve real efficiency and total control.
WHAT WE DO
From data integration to predictive quality, Appliant MIP optimizes every stage of the process to achieve real efficiency and total control.
Appliant Manufacturing Intelligence Platform (MIP)
Breaking data silos to increase your operational efficiency. In a GMP compliant way.
Appliant Manufacturing Intelligence Platform
- Real Time Dashboarding
- Advanced Analytics
- Historian
- Audit Trail
- Active Directory
- FDA 21 CFR Part 11
- EU GMP Annex 11
- GAMP5 software category 4
- VDI/VDE/NAMUR 2658
- Cybersecure IEC 62443
A single platform with all production data, validated 01
Manufacturing Intelligence Platform (MIP) breaks down the plant’s data silos.
It centralizes all your data in the Appliant MIP platform (Manufacturing Intelligence Platform) and obtains a comprehensive view with native connectivity to ERP (Enterprise Resource Planning) and QMS (Quality Management System).
Product Quality Review (PQR), in real time 02
By having all production data on the same platform, a PQR report is generated automatically in real time. Take action before problems occur.
With the Real Time Product Quality Review (RTPQR) app, conduct proactive quality reviews and avoid deviations before they impact your production.
Robust and consistent processes 03
Assure the robustness of your operations using CPV 4.0 (Continuous Process Verification).
Implement PAT technologies with the Appliant CPV 4.0 Process Analytical Technology app (PAT_app) and guarantee continuous verification with full regulatory compliance.
Faster batch release to assure final quality 04
Detect and correct deviations instantly.
With Real Time Release (RTR), anticipate the detection of defective batches thanks to AI and comparative analysis, saving time and reducing operational costs.
HOW WE DO
We've packed 15+ years of biopharma manufacturing expertise into apps GMP compliant.
Seamless integration
Connect equipment
from different
suppliers smoothly.
Quick launch
Reduce start-up
and validation times.
Freedom to scale up
We adapt the installation
to the plant’s digital maturity,
timescales and workforce.
Modular design
Flexible architecture that complies
with the principles of
Pharma 4.0 architecture.