Revamped Pharmaceutical Technology Upgradation Assistance Scheme
Elevating India’s Pharma Sector to Global Compliance Standards
Revamped Pharmaceutical Technology Upgradation Assistance Scheme
The Revamped Pharmaceutical Technology Upgradation Assistance Scheme, introduced by the Department of Pharmaceuticals (Government of India), aims to support the modernization of India’s pharmaceutical manufacturing landscape by helping MSMEs adopt WHO-GMP (World Health Organization-Good Manufacturing Practices) and Schedule M standards.
With a tiered capital subsidy structure based on turnover brackets, the scheme enables eligible pharma companies to invest in benchmark manufacturing technologies, thereby enhancing regulatory compliance, global market access, and production efficiency.
At DharmaSetu Goldschmidt Advisory, we offer deep industry-aligned consulting to help you plan, apply, and receive capital subsidies under this critical scheme—transforming your upgrade into a competitive advantage.
Scheme Objectives
- Encourage technology upgradation and modernization in pharmaceutical MSMEs
- Promote compliance with international standards (WHO-GMP, Schedule M)
- Enable manufacturers to become export-ready and meet global regulatory benchmarks
- Strengthen India’s positioning as a global hub for safe, effective, and high-quality medicines
Eligible Beneficiaries
- Micro, Small, and Medium Enterprises (MSMEs) involved in pharmaceutical manufacturing
- Units with annual turnover below ₹500 crore (average of the last 3 financial years)
- Entities seeking to upgrade to WHO-GMP or Schedule M compliance standards
Eligible Activities
- Procurement of new machinery and production equipment required to meet Schedule M or WHO-GMP standards
- Installation and commissioning of critical utilities, cleanroom equipment, quality control tools, HVAC systems, etc.
- Technical retrofitting of plants for environmental and biosafety compliance
- Implementation of electronic batch tracking and data integrity systems
Applicable Benefits
Annual Turnover (Avg. of Last 3 Years) | Capital Subsidy | Maximum Subsidy Cap |
₹1 Crore to ₹50 Crore | 20% | ₹1 Crore |
₹50 Crore to ₹250 Crore | 15% | ₹1 Crore |
₹250 Crore to ₹500 Crore | 10% | ₹1 Crore |
Subsidy applies to eligible machinery and equipment costs only
Available for both API (Active Pharmaceutical Ingredient) and formulation manufacturers
Our Advisory Support Includes
- Eligibility assessment and turnover validation
- Technical alignment of plant layout and machinery list with WHO-GMP norms
- Preparation of subsidy application, DPR (Detailed Project Report), and CAPEX breakdown
- Vendor certification and documentation validation
- Advisory with DoP, SIDBI, and participating financial institutions
- Support with post-installation verification and subsidy disbursement
Why Work with DharmaSetu Goldschmidt Advisory?
- Specialist experience across Formulations, APIs, Biologics, and Ayurvedic Pharma
- In-depth familiarity with Schedule M, WHO-GMP, and regulatory alignment frameworks
- Technical partners and architects who understand pharma production flows
- End-to-end guidance—from subsidy strategy to funds receipt
- Ethical, efficient, and transparent consulting model trusted across pharma corridors
Frequently Asked Questions
We offer end-to-end support — from eligibility checks and project documentation to application filing and departmental coordination — ensuring maximum benefits with minimal hassle.
We provide consultancy for a wide range of government subsidies — including those for agriculture, manufacturing, MSMEs, technology upgrades, clean energy, exports, and infrastructure development.
Yes, we serve clients nationwide. We’ve successfully helped over 750+ enterprises across sectors and geographies secure government incentives and capital-linked support.
Timelines vary based on the type of subsidy and department workload. However, our team actively tracks and manages your application to ensure accelerated clearance and faster disbursal.
Requirements vary by scheme, but usually include:
- Business registration documents
- Financial statements and projections
- Project reports / DPRs
- Environmental or utility clearances (if applicable)
We provide you with a customized checklist and assist at every stage.