Proventus’s commitment to quality resides upon the steady foundations of policy built by our admirable skills and hard work.

Quality Assurance
We benchmark against global excellence in every aspect, strive for continuous improvement in all our processes and focus on people-oriented policies and practices. Additionally, we proactively ensure to meet applicable regulatory and statutory requirements. With a clear intent to add value to our stakeholders, we drive excellence and quality.
- Quality Risk Assessment
- Change & Deviation Control
- Root Cause Investigation
- Calibration Programme
- Equipment Qualification
- Self Inspection
- APQR
- Ensuring cGMP Compliances
- Market Compliant Investigation
- OOS Investigation
- Preventive Maintenance
- Documents Control
- Vendor Approvals
- Training Programme
QC Capabilities
- Analytical Method Development
- Analytical Method Validation
- Analytical Transfer
- API and Impurities Qualification
- Impurity Profiling
- Genotoxic AMV
- Nitrosamine Assessment
- Filing and Post-filing Support
- Troubleshooting Analytical Challenges
- Stability Study
- Forced Degradation Study


QC Instrumentation
- HPLC with PDA and UV
- GC-HS with FID
- UV-Vis Spectrophotometer
- Auto Titrator
- Stability Chambers
Find Your Perfect API
With our customisable options, you can unlock the right API formula that aligns with your project requirements and therapeutic goals.