Transfer-pricing treatment of ITeS margins excludes pass-through tax recoveries and separate delayed-receivables interest after working-capital adjust...
Capacity-utilisation adjustments under TNMM can neutralise substantiated COVID-related idle costs where underutilisation materially affects profitabil...
TNMM functional comparability requires excluding rice manufacturers from a pure Basmati rice trader's benchmark and recognising operating export recei...
Working-capital adjustment subsumes delayed-receivable effects in TNMM benchmarking of captive software-development services, avoiding separate notion...
Transfer-pricing comparability requires exclusion of financially illogical super-profit comparables and correction of unsupported annual-report and ma...
Charitable character assessment preserves Section 80G approval despite inclusive spiritual teachings and incidental religious expenditure within the s...
Penalty proceedings for cash-loan acceptance require assessment proceedings and recorded Assessing Officer satisfaction; absent these, the proceedings...
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DGFT issued Trade Notice 06/2025-26 establishing a one-time quota allocation of 25,000 MT for Pharma Grade Sugar exports under restricted category for the current sugar season ending September 30, 2025. Applications must be submitted online through DGFT's ECOM system between June 20-July 20, 2025. Eligibility requires valid drug manufacturing license from State Licensing Authority and PHARMEXIL membership with valid RCMC. Quota allocation follows pro-rata basis based on production capacity. Export authorizations remain valid for one year with mandatory NABL-accredited laboratory certification confirming pharma grade specifications at export time. Only one application per IEC considered, with deficient or late applications rejected.
DGFT issued Trade Notice 06/2025-26 establishing a one-time quota allocation of 25,000 MT for Pharma Grade Sugar exports under restricted category for the current sugar season ending September 30, 2025. Applications must be submitted online through DGFT's ECOM system between June 20-July 20, 2025. Eligibility requires valid drug manufacturing license from State Licensing Authority and PHARMEXIL membership with valid RCMC. Quota allocation follows pro-rata basis based on production capacity. Export authorizations remain valid for one year with mandatory NABL-accredited laboratory certification confirming pharma grade specifications at export time. Only one application per IEC considered, with deficient or late applications rejected.
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