Subsidiary formation for pharma and medical-device companies
Foreign companies usually set up a wholly owned private limited company for manufacturing, distribution or R&D. We handle incorporation and FDI compliance, and advise on how the corporate structure interacts with licences under the Drugs and Cosmetics Act.
Subsidiary Formation
Transfer pricing for clinical trials and R&D
Contract research, clinical-trial agreements and R&D cost-sharing with overseas affiliates must be priced at arm's length. We benchmark R&D services, IP licensing and data-sharing arrangements and defend positions in TP assessments.
Transfer Pricing
GST for medical devices and pharmaceutical products
Rates vary widely: many life-saving medicines are at 5% or nil, while devices attract rates from 5% to 18% depending on HS classification. Healthcare services are largely exempt, but digital health, diagnostics and medical-tourism facilitation can be complex. We manage classification, registration and filings.
GST & Indirect Tax
FEMA compliance for healthcare FDI Verify
Healthcare FDI has specific conditions, which differ for greenfield and brownfield pharmaceutical investment; brownfield acquisitions above the automatic-route limit need Government approval. We advise across hospitals, diagnostics, pharma and devices and handle FC-GPR, APR and capital-account reporting.
FEMA & RBI Compliance
Virtual CFO for healthcare startups and scale-ups
Digital-health startups, diagnostic chains and medtech companies need finance leadership that understands capex-heavy infrastructure, regulated pricing and insurance reimbursement cycles. We provide monthly financial management, board reporting and investor-grade compliance.
Virtual CFO