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