Regulatory Lifecycle Management
Streamline compliance from development to market.
- Development Phase Support
- Regulatory Submissions
- Approval Monitoring
- Post-Market Compliance
Dossier Preparation (CTD/eCTD/DMF)
Ensure seamless document submission for global regulatory approvals.
- CTD/eCTD Formatting
- DMF Compilation
- Global Submission Standards
- Document Validation
Regulatory Approvals Support
Navigate complex approval processes efficiently with expert guidance.
- Application Review
- Regulatory Consultation
- Approval Strategy
- Timely Submissions
WHO-GMP Certification Support
Achieve and maintain WHO-GMP certification with compliance assistance.
- GMP Audit Preparation
- Quality Management Systems
- Certification Guidance
- Post-Certification Support
CDSCO Compliance Assistance
Simplify CDSCO regulatory filings for smooth market entry in India.
- CDSCO Application Filing
- Local Regulatory Insights
- Compliance Documentation
- Market Authorization
US FDA Regulatory Submission Support
Ensure accurate submissions to meet US FDA compliance standards.
- FDA Pre-Submission Support
- Regulatory Dossier Preparation
- Compliance Review
- Submission Tracking
Pharma Import-Export Licensing Assistance
Obtain necessary licenses for seamless global trade operations.
- Import/Export Application
- Licensing Documentation
- Trade Compliance Support
- Regulatory Liaison
AI-Powered Regulatory Compliance Monitoring
Automate compliance tracking with advanced AI solutions.
- Real-Time Monitoring
- Data-Driven Insights
- Automated Reporting
- Regulatory Alerts
AI-Driven GMP Audit Management
Enhance GMP audit efficiency with AI-driven process optimization.
- AI Audit Preparation
- Real-Time Analysis
- Compliance Scorecards
- Corrective Action Plans