Accounting, Audit & Ind AS

Ind AS 38: Intangible Assets — Recognition, Amortisation & Impairment

Ind AS 38 – Intangible Assets
CA Nikhil Gupta·June 2026·14 min readICAI / MCAInd AS Series
StandardInd AS 38Ind AS 38: Intangible Assets — Recognition, Amortisation & ImpairmentMCA Notification ↗
📄 In This Article
  1. What Is an Intangible Asset? Core Criteria
  2. Recognition: Acquired vs Internally Generated
  3. The R&D Rule: Research Always Expensed, Development Maybe Capitalised
  4. Amortisation: Finite vs Indefinite Useful Life
  5. Impairment of Intangibles
  6. Case Study: TCS — Software Development Capitalisation
  7. Case Study: Sun Pharma — Drug Discovery R&D
  8. Case Study: Hindustan Unilever — Acquired Brands & Trademarks
  9. Comparison: Ind AS 38 vs Old IGAAP
  10. Key Disclosures Required Under Ind AS 38

Ind AS 38 governs accounting for intangible assets — identifiable non-monetary assets without physical substance. From capitalised software development costs to acquired brand names, drug licences to customer relationships recognised in a business combination, intangibles are central to the balance sheets of India's knowledge-economy companies. The standard draws a sharp line between what can be recognised as an asset and what must be expensed — and the consequences are significant for reported EBITDA, profit, and balance sheet strength.

📑 Paragraph-wise structural breakdown: a plain-language map of how this standard's content typically flows, to orient you before reading the official text. This is Finin2min's structural explanation, not verbatim official paragraph numbers — always confirm exact wording and numbering against the Companies (Indian Accounting Standards) Rules, 2015 and subsequent amendment notifications.
Structural blockWhat it covers
Objective and scopePrescribes accounting for intangible assets — identifiable, non-monetary assets without physical substance (patents, software, licences, customer relationships) — not specifically dealt with in another standard.
Identifiability and recognitionAn intangible asset must be identifiable (separable, or arising from contractual/legal rights), controlled by the entity, and expected to generate future economic benefits — recognised only when cost can be measured reliably and the recognition criteria are met.
Internally generated intangiblesResearch costs are always expensed as incurred; development costs are capitalised only once the entity can demonstrate technical feasibility, intention and ability to complete and use/sell the asset, and reliable cost measurement — internally generated goodwill, brands, and similar items are never recognised as assets.
Measurement after recognitionCost model (cost less accumulated amortisation and impairment) or, rarely used in India, revaluation model where an active market exists.
Useful life and amortisationAssets with a finite useful life are amortised systematically over that life; assets with an indefinite useful life are not amortised but are tested for impairment at least annually (per Ind AS 36) and the "indefinite" assessment is reviewed each period.
Derecognition and disclosureDerecognised on disposal or when no future economic benefits are expected; disclosures include a reconciliation of carrying amount by class, and separate disclosure of the aggregate research and development expenditure recognised as an expense.

What Is an Intangible Asset? Core Criteria

Under Ind AS 38, an intangible asset is an identifiable non-monetary asset without physical substance. Three conditions must all be met:

  1. Identifiability: Separable from the entity (can be sold, transferred, licensed independently), OR arises from contractual/legal rights (even if inseparable)
  2. Control: Entity has power to obtain future economic benefits from the resource and can restrict others' access
  3. Future economic benefits: Expected inflow of revenues, cost savings, or other economic benefits attributable to the asset

Examples: patents, copyrights, customer lists, software licences, brand names (acquired), franchise rights, customer relationships, drug approvals (ANDA, NDA), mining rights.

Not intangible assets under Ind AS 38: Goodwill arising from business combinations (governed by Ind AS 103), financial assets (Ind AS 109), deferred tax assets (Ind AS 12), and assets arising from insurance contracts. Internally generated goodwill, brands, mastheads, customer lists cannot be recognised as assets — they must be expensed.

Recognition: Acquired vs Internally Generated

Recognition depends critically on whether the intangible was acquired externally or generated internally.

SourceRecognitionInitial Measurement
Separately acquired (e.g., patent purchased)Recognised as asset if identifiable, controllable, future benefits probableCost = purchase price + directly attributable costs to prepare for intended use
Acquired in business combination (Ind AS 103 PPA)Recognised separately from goodwill if fair value can be reliably measuredFair value at acquisition date (even if not on acquiree's balance sheet)
Internally generated (brand, masthead, customer list)Cannot be recognised — always expensedN/A
Internally generated — development phase (qualifying)Recognised if all 6 criteria met (see below)Directly attributable costs from date criteria first met
Received as government grantCan recognise at fair value or nominal amountPer Ind AS 20

The R&D Rule: Research Always Expensed, Development Maybe Capitalised

This is the most practically important part of Ind AS 38 for pharma, tech, and industrial companies. The standard distinguishes research from development:

Research Phase

Original, planned investigation to obtain new scientific/technical knowledge and understanding

Always expensed — no exceptions. Cannot be capitalised regardless of outcome probability.

Examples: laboratory studies, testing of alternatives, searching for new knowledge

Development Phase

Application of research findings to plan/design new or substantially improved products/processes

Capitalised only if ALL 6 criteria are met

Examples: prototype testing, design of tools/jigs/dies, pilot plant design

The 6 Development Capitalisation Criteria (All Must Be Met)

  1. Technical feasibility of completing the intangible so it will be available for use or sale
  2. Intention to complete and use/sell it
  3. Ability to use or sell the asset
  4. Probable future economic benefits — demonstrated by existence of a market or internal usefulness
  5. Adequate technical, financial and other resources to complete development
  6. Ability to reliably measure expenditure attributable to the intangible during development
Phase segregation is challenging in practice: Many R&D projects seamlessly transition from research to development. Ind AS 38 requires entities to allocate expenditure between phases — but where the line is unclear, the expenditure must be treated as research (i.e., expensed). This creates significant judgement and is an area of audit scrutiny.

Amortisation: Finite vs Indefinite Useful Life

The amortisation treatment depends on the useful life classification:

CategoryUseful LifeAmortisationImpairment Testing
Finite useful lifeDeterminable (years or units of production)Amortised systematically over useful life; reviewed annuallyOnly when impairment indicators exist
Indefinite useful lifeNo foreseeable limit to period of economic benefitsNOT amortisedAnnual impairment test required (even without indicators)

Residual value of a finite-life intangible is assumed to be zero unless:

Amortisation method: Must reflect the pattern of consumption of expected economic benefits. Straight-line is most common; units-of-production can be used if usage pattern is determinable.

✓ Common useful lives in India (Ind AS 38):
  • Capitalised software (development costs): 3–5 years
  • Customer relationships (from PPA): 5–15 years
  • Patents: remaining legal life or economic life, whichever is shorter
  • Drug approvals/ANDAs: economic life (typically 10–20 years)
  • Brand names (finite): per contractual/market assessment
  • Brand names (indefinite): no amortisation; annual impairment test

Impairment of Intangibles

Impairment of intangibles is governed by Ind AS 36 (Impairment of Assets). Key points:

See our Ind AS 36 guide for the full impairment methodology.

Case Study: TCS — Software Development Capitalisation

💻 TCS: Internal-Use Software Development Costs

Tata Consultancy Services | Ind AS 38 Application | FY 2024–25

TCS, India's largest IT company, develops significant proprietary software platforms — including its BaNCS banking platform, Ignio AI, and various industry-specific solutions. How does Ind AS 38 apply?

Research Phase (Expensed)
Initial market research, feasibility studies, proof-of-concept exploratory work
Development Phase (Capitalised if criteria met)
Detailed design, coding, testing of defined product — once technical feasibility established
Typical Useful Life
3–5 years for application software; 5–7 years for platform software
TCS Disclosure (FY25)
Software (intangibles) carried at cost less amortisation; amortised over 3–5 years on straight-line basis

TCS's FY25 annual report shows ₹1,200+ crore in intangible assets (software and IP), amortised at approximately ₹400–500 crore per year. Internal-use software that doesn't meet Ind AS 38 development criteria is expensed in the same period — creating a conservative earnings impact in development years.

Case Study: Sun Pharma — Drug Discovery R&D

💊 Sun Pharmaceutical: ANDA Portfolio & R&D Treatment

Sun Pharmaceutical Industries | Ind AS 38 Application | FY 2024–25

Sun Pharma's competitive advantage lies in its ANDA (Abbreviated New Drug Application) pipeline and specialty drug portfolio. Ind AS 38 applies differently to different types of pharma intangibles:

Intangible TypeInd AS 38 TreatmentBalance Sheet Impact
Acquired ANDAs / product rightsCapitalised at acquisition cost; finite useful lifeYes — significant asset on balance sheet
In-house ANDA filing costsResearch phase = expensed; development capitalised only post-approval likelihood establishedLimited — most expensed
Specialty pharma brands (acquired)Capitalised; typically indefinite life if strong brand equityYes — subject to annual impairment test
Internal drug discovery (early stage)Always expensed — research phaseNo — P&L impact only

Sun Pharma's FY25 balance sheet carries ₹8,000–10,000 crore in intangible assets, predominantly from acquired branded generics businesses (Ranbaxy merger, Halol acquisitions). Their R&D spend of ₹3,500+ crore in FY25 is largely expensed — creating a drag on reported EBITDA but building future pipeline value not visible on the balance sheet.

FY25 R&D Spend
~₹3,600 crore (~8.5% of revenue)
Portion Capitalised
Minimal — most in research phase
Intangibles on Balance Sheet
~₹9,200 crore (FY25)
Amortisation per year
~₹1,200 crore (impacts reported PAT)

Case Study: Hindustan Unilever — Acquired Brands & Trademarks

🌄 HUL: Brand Accounting Under Ind AS 38

Hindustan Unilever Limited | Ind AS 38 Application | FY 2024–25

HUL owns iconic brands like Surf Excel, Lux, Dove, Lifebuoy, Horlicks (acquired from GSK Consumer). How are these brands treated?

Key principle: Internally developed brands (built organically by HUL over decades — Surf, Lux, Lifebuoy) cannot be capitalised under Ind AS 38. They are not on HUL's balance sheet at all — regardless of their economic value running into thousands of crores.

Acquired brands (Horlicks, Boost, Viva — acquired via the GSK Consumer Healthcare acquisition in 2020) are capitalised at their fair value on the acquisition date.

Brand CategoryBalance Sheet?Ind AS 38 Treatment
Horlicks, Boost (acquired)Yes — at acquisition FV (~₹8,000+ crore)Indefinite useful life; no amortisation; annual impairment test
Surf Excel, Lux, Dove (organic)NoCannot be recognised — internally generated brand

This creates the famous "brand gap" — HUL's market cap of ~₹5-6 lakh crore vs book value of ~₹9,000 crore. The difference largely represents organic brand value + franchise not captured in IGAAP/Ind AS financial statements.

Comparison: Ind AS 38 vs Old IGAAP

Old IGAAP (AS 26)
  • Goodwill from acquisitions could be amortised or written off against reserves
  • R&D capitalisation criteria were less rigorous — more flexible
  • Useful life of intangibles presumed not to exceed 10 years (rebuttable)
  • Indefinite useful life concept less explicitly defined
  • Revaluation of intangibles generally not permitted
Ind AS 38
  • Goodwill NOT amortised (Ind AS 103) — annual impairment test only
  • Strict research vs development distinction; research always expensed
  • No presumptive useful life cap — assessment based on facts
  • Indefinite useful life explicitly recognised; no amortisation
  • Revaluation model available (requires active market — rare for intangibles)

Key Disclosures Required Under Ind AS 38

Companies must disclose for each class of intangible assets:

Journal Entries: Capitalised Software Development Costs
Dr Intangible Asset — Software Development
₹50,00,000
    Cr Salaries & Wages Payable (directly attributable)
₹40,00,000
    Cr Third-party Development Costs Payable
₹10,00,000
Annual Amortisation (over 5-year useful life)
Dr Amortisation — Software Development
₹10,00,000
    Cr Accumulated Amortisation — Software
₹10,00,000
Research Expenditure (always expensed)
Dr Research & Development Expense
₹25,00,000
    Cr Salaries / Vendor Payable
₹25,00,000

Frequently Asked Questions

Can a company capitalise internally developed brand value under Ind AS 38?
No. Ind AS 38 explicitly prohibits recognition of internally generated brands, mastheads, publishing titles, customer lists, and similar items as intangible assets. The standard concludes that expenditure on these items cannot be distinguished from the cost of developing the business as a whole. This is why HUL's iconic organic brands (Surf, Lux, Dove) are not on its balance sheet despite being worth tens of thousands of crores in market value. Only brands acquired from third parties (through purchase or business combination) can be recognised.
When can a pharma company capitalise drug development costs under Ind AS 38?
A pharma company can capitalise drug development costs only after it can demonstrate all six Ind AS 38 development criteria simultaneously — including technical feasibility (typically established only after Phase 2/3 clinical trial success), intention to complete, ability to use/sell, probable economic benefits (regulatory approval with commercial market), adequate resources, and reliable measurement. In practice, given the high failure rates in pharma R&D and regulatory uncertainty, most companies expense all pre-approval drug development costs. Capitalisation typically begins only after regulatory approval or at very late-stage development with high approval probability.
What is the difference between amortisation and impairment for intangibles?
Amortisation is the systematic allocation of the cost of a finite-life intangible asset over its useful life — it's a planned, predictable charge that reduces the carrying amount each period regardless of market conditions. Impairment is a sudden, unplanned write-down triggered when the carrying amount exceeds the recoverable amount (due to market changes, obsolescence, legal challenges, etc.). Both reduce the intangible's carrying amount, but amortisation is budgeted and expected; impairment reflects unexpected deterioration. Indefinite-life intangibles are not amortised at all but must be tested for impairment annually — so impairment is the only mechanism that reduces their carrying amount.

Source and review trail

Use the current official instrument, portal or regulator publication before acting. This panel separates the category authority from page-specific references.

Primary category
Accounting, Audit & Ind AS
Official starting point
www.icai.org
Editorial review date
2026-07-19
Content status
Finin2min explanation; official source controls where facts, law, rates, forms or procedures can change.

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