Global Expertise. Local Solutions. Your Gateway to Compliance Excellence.
We have been working in India for over 40 years
India is a global leader in pharmaceuticals, APIs, and generics, with an ever-expanding footprint in regulated markets. At Lachman Consultants, we help Indian manufacturers and exporters navigate complex international regulations, strengthen compliance systems, and achieve sustainable growth.
Why Choose Lachman in India?
Unmatched Regulatory Expertise: Decades of experience with U.S. FDA, EMA, MHRA, and other global agencies.
Proven Track Record: Trusted by top pharma companies worldwide for inspection readiness and compliance.
Tailored Solutions: Strategies designed for Indian operations with global standards in mind.
Core Services for India:
Quality & Compliance
- Regulatory Response and Remediation Support
- GMP Audits and Compliance Assessments
- Data Integrity Audits
- Quality Systems Development and Optimization
Inspection Readiness
- Mock FDA audits
- Pre-approval inspection preparation
- Post-inspection corrective action planning
Training & Education
- Customized QA/QC training programs
- Global compliance workshops
- Leadership development for regulatory excellence
Regulatory Consulting
- ANDA, NDA, DMF preparation and submissions
- U.S. FDA and EU regulatory strategy
- Lifecycle management for generics and APIs
