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Government implementing authority

Revamped Pharmaceutical Technology Upgradation Assistance Scheme (RPTUAS)

Capital subsidy of 10% to 20% of eligible pharmaceutical-upgradation investment, subject to INR 2 crore maximum

Subsidies & incentives Subsidy Paused: no open call right now
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What it is

Facilitate existing pharmaceutical units in upgrading manufacturing technology and facilities to meet Revised Schedule M and WHO-GMP standards.

What you get

  • Capital subsidy of 10% to 20% of eligible pharmaceutical-upgradation investment, subject to INR 2 crore maximumUp to ₹2,00,00,000

Who it is for

  • Existing pharmaceutical manufacturing unit with a proven operating track record
  • Average turnover for the preceding three years must be below INR 500 crore
  • Unit must be upgrading toward Revised Schedule M and/or WHO-GMP standards
  • Eligible expenditure must be incurred after 01 January 2024
  • Current scheme intake and shortlisted-applicant status must be confirmed from the Department/SIDBI route
  • CA-certified expenditure and the applicable regulatory certificate are required for staged claims
Pharmaceutical manufacturing unitPharma msmePharma smeOperatingScalingExportingPharmaceuticalsBulk drugsPharmaceutical formulationsManufacturingIndia

How to apply

  1. 1
    Confirm current intake and applicant boundary

    Check with the Department of Pharmaceuticals or SIDBI that applications are being accepted for your unit's category.

    Official step
  2. 2
    Classify turnover and eligible investment

    Calculate the preceding-three-year average turnover and isolate post-01 January 2024 expenditure in eligible activities and production equipment.

  3. 3
    Prepare certification and technical dossier

    Prepare the CA-certified expenditure statement, project or gap-analysis material and the Revised Schedule M/WHO-GMP certification sequence required by the current modification.

    Official step
  4. 4
    Submit through the verified official route

    Submit your dossier on the official Department/SIDBI scheme portal, then track the technical review, the Scheme Steering Committee decision and the staged release of funds.

    Official step

Keep ready

Existing pharmaceutical manufacturing unit, preceding-three-year average turnover evidence, post-01 January 2024 eligible-investment records, CA-certified expenditure, facility-upgradation plan and applicable regulatory certification