At complypharma.ai, we offer AI-powered compliance solutions for pharma and biotech, streamlining regulatory processes and enhancing risk detection globally.
ComplyPharma’s AI-Powered Dossier Validation reduces regulatory errors by 60% and boosts approval success rates for WHO-GMP, US FDA, and CDSCO.
As a Investment firm our main goal is to provide best services to our customers & create best ideas to help grow our clients.
Regulatory Lifecycle Management
- Development Phase Support
- Regulatory Submissions
- Approval Monitoring
- Post-Market Compliance
Dossier Preparation (CTD/eCTD/DMF)
- CTD/eCTD Formatting
- DMF Compilation
- Global Submission Standards
- Document Validation
Regulatory Approvals Support
- Application Review
- Regulatory Consultation
- Approval Strategy
- Timely Submissions
WHO-GMP Certification Support
- GMP Audit Preparation
- Quality Management Systems
- Certification Guidance
- Post-Certification Support
CDSCO Compliance Assistance
- CDSCO Application Filing
- Local Regulatory Insights
- Compliance Documentation
- Market Authorization
US FDA Regulatory Submission Support
- FDA Pre-Submission Support
- Regulatory Dossier Preparation
- Compliance Review
- Submission Tracking
Accelerating global pharma compliance with AI-driven solutions.
Ensuring accuracy for WHO-GMP, US FDA, and CDSCO submissions.
Supporting pharma expansion across the US, EU, UAE, and India.
Dedicated to error-free, AI-powered processes.
Want to Fast-Track Your Pharma Approvals? Call – +91 77020 21948
We believe in a future where AI-driven solutions revolutionize regulatory compliance, ensuring efficiency and accuracy. At ComplyPharma.ai, we offer innovative regulatory services, streamlining compliance for a sustainable pharmaceutical industry.
At ComplyPharma, we envision a future where AI-powered compliance accelerates global pharmaceutical approvals. Our solutions ensure accuracy, efficiency, and sustainability in every step.
Your Questions, Our Answers
At ComplyPharma, we simplify global pharmaceutical compliance with AI-driven solutions, ensuring smooth regulatory approvals.
Do we need documentation for regulatory submissions?
Yes, we assist in preparing AI-optimized regulatory filings tailored for WHO-GMP, US FDA, and CDSCO standards.
What is the cost of your compliance services?
Pricing depends on the scope — from regulatory strategy to AI-powered document validation. Contact us for custom quotes.
How long does the approval process take?
Timelines vary by authority, but our AI tools speed up documentation review and submission.
What payment methods do you accept?
We support bank transfers, credit cards, and corporate billing.
Can you review previously submitted filings?
Absolutely! We audit past submissions to identify gaps and optimize for re-approval.
How many regulatory pathways do you support?
We cover major pathways for US FDA, EMA, WHO-GMP, CDSCO, and emerging markets.
Which regions do you cover?
We work with regulatory authorities in the US, EU, India, UAE, and more.
Our Latest Case Studies
At ComplyPharma, we empower pharmaceutical companies with AI-driven compliance solutions, ensuring seamless regulatory approvals.
August 31, 2023
August 29, 2023
August 29, 2023