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10 of 42 filings·Updated 24 Aug 2026
Showing 10 of 42 filings.
24 Aug 20261 filing
Company UpdateEarnings Call Transcript

Orchid Pharma Q1 FY27: Revenue 304 cr, margin 33%, capex for 7-ACA and Cefiderocol; multiple project milestones ahead

Financial Performance

  • Q1 FY27 revenue from operations: INR 304 crores; ~15% YoY growth.
  • Q1 FY27 gross margin: 33%; Q1 FY26: ~30%.
  • Q1 FY27 EBITDA: INR 25 crores; Q1 FY26: INR 10 crores.
  • FY26 revenue from operations restated: INR 1,233 crores; FY25: INR 1,398 crores.
  • Capex FY27: INR 750 crores for 7-ACA; Cefiderocol capex: USD 20–25 million.
  • 7-ACA ramp-up: ~80% in-house, 20% third-party output.
  • Cefiderocol readiness: facility ready by Dec 2026; validation and initial batches Jan–Mar 2027; DCGI waiver possible.
  • Russia license Exblifep: estimated 10-year value USD 178 million.
  • AMS division: Q1 EBITDA loss ~ INR 0.5 crores; revenue INR 5 crores.
  • NP-NC segment quarterly revenue: INR 21 crores.
  • Russia registration/launch timeline: 1.5–2 years from signing.
  • 7-ACA revenue contribution expected from FY28.

Operations and Markets

  • Exblifep progress in Russia valued at USD 178 million over 10 years.
  • Europe volumes growth shown; Q3 FY26 up 300% QoQ, Q4 FY26 up 170%, Q1 FY27 up 50%.
  • Middle East/Africa: South Africa registration complete; GCC coverage; launches delayed by regional conflict.
  • 7-ACA facility ramp in Jammu chosen for cost efficiencies (GST benefits, electricity/water advantages).
  • Cefepime-Enmetazobactam: domestic supply currently from in-house manufacturing; export via CMO.

Projects and Capital Expenditure

  • 7-ACA capex: INR 750 crores; commissioning by March 2027.
  • Cefiderocol capex: USD 20–25 million.
  • Cefiderocol readiness: December 2026; first validation/batches Jan–Mar 2027.
  • Russia licensing: agreement signed; registration dossier 1.5–2 years to launch.

Q&A Highlights

  • 7-ACA ramp-up target: 12 months to stabilize; 80% in-house, 20% third-party use.
  • Cefiderocol: supplies initially via China-based CMO; potential in-house manufacturing after site validation.
  • US filings plan: new molecules planned; annual updates; limited quarterly detail.
  • NZ/Global strategy: Cefide­rocol distribution network being built; GARDP discussions for distribution.

Guidance and Outlook

  • No formal FY27 numeric guidance provided; expects regulated market demand to improve over 2–3 quarters.
  • Longer-term outlook supported by merger synergies, product mix improvements, and capital Projects.
Filed 18:19View Source
21 Aug 20261 filing
Company UpdateAnalyst / Investor Meet

Orchid Pharma uploads audio recording of Aug 21, 2026 analysts/investors earnings call

Meeting Details

  • Date and time: August 21, 2026, 15:00 IST.
  • Type and mode: group earnings call, audio conference.
  • Event: Analysts/Investors Earnings Call hosted by Orchid Pharma Limited.
  • Key company participant: Company Secretary & Compliance Officer.
  • Purpose: discuss unaudited/limited-reviewed Q1 FY2026-27 results.
  • Recording: audio recording uploaded on company's website; no video recording.
Filed 20:18View Source
20 Aug 20261 filing
Company UpdateAnalyst / Investor Meet

Orchid Pharma Announces NCLT-Sanctioned Amalgamation of Dhanuka Laboratories into Orchid Pharma

Corporate action

  • Dhanuka Laboratories Ltd. amalgamated into Orchid Pharma Ltd. under the NCLT-sanctioned Scheme.
Filed 17:54View Source
17 Aug 20261 filing
Company UpdateAnalyst / Investor Meet

Orchid Pharma to hold Q1FY27 results conference call on 21 Aug 2026 organized by Systematix Institutional Equities

Meeting Details

  • Q1FY27 results conference call for Orchid Pharma Limited on Friday, 21 August 2026 at 3:00 PM IST.
  • Organizer: Systematix Institutional Equities invites participation.
  • Management participants: MD, Whole Time Director, CFO.
  • Mode: virtual conference call with dial-in options.
  • Purpose: discuss Q1FY27 results.
Filed 18:51View Source
14 Aug 20262 filings
Company UpdateReg. 32 (1), (3) - Statement of Deviation & Variation

QIP funds deviation approved by shareholders with revised allocations amid project delays

Deviation details

  • Mode of fund raising: Qualified Institutions Placement (QIP).
  • Deviation exists and was approved by shareholders via AGM.
  • Reason for deviation: business environment changes; reallocation to meet strategic needs; Jammu API postponed.
  • Modified allocation objects: OBPL Jammu facility; debt repayment; Alathur API facility; general corporate purposes.
  • Shareholder approval obtained via AGM.
  • Monitoring agency: Care Ratings Limited.
  • Audit committee comments: Annexure.
  • Auditors: not applicable.
  • Utilisation status: revised allocations being utilised; Jammu facility delayed.
  • Major change: allocations reallocated among key objects per AGM approval.
Filed 20:11View Source
Company UpdateMonitoring Agency Report

AGM-approved revision of QIP proceeds; Jammu facility delayed and funds partially unutilised

Issue Overview

  • Type of issue: QIP of equity shares.
  • Total issue size; net proceeds revised; no undersubscription.
  • Objectives include OBPL Jammu facility, debt repayment, Alathur API facility, and general corporate purposes.

Utilisation of Proceeds

  • Utilisation aligned with revised allocation approved by AGM on Sep 20, 2025.
  • Shareholder approval obtained for revised allocations.
  • Means of finance changed via revised allocation; AGM approval obtained.
  • No major deviation from earlier MA report.
  • Statutory approvals not specified; AGM notes no further Alathur investment from QIP proceeds.
  • Technical know-how: Rs 10 crore allocated; Rs 3.77 crore spent.
  • OBPL Jammu facility: significant delay; commercial operations expected Feb 2027.
  • Repayment of borrowings: largely allocated and utilised.
  • Alathur API facility: minimal utilisation; no unutilised balance.
  • Unutilised funds parked in fixed deposits; interest transferred to cash credit account.

Governance & Compliance

  • Shareholder approval obtained via AGM Sep 20, 2025.
  • No explicit statutory approvals listed; AGM notes no further Alathur investment.
  • Delay in Jammu project; commercial operations expected Feb 2027.
  • Unutilised funds parked in fixed deposits; interest credited to cash credit.

GCP

  • GCP revised to 63.72 crore due to higher net proceeds.
  • GCP fully utilised; completed as of Mar 31, 2025.
  • Board approval obtained for revised allocations via AGM Sep 20, 2025.
Filed 19:03View Source
11 Aug 20261 filing
Board Meeting

Orchid Pharma Ltd board meeting scheduled; no agenda details disclosed

Orchid Pharma Ltd board meeting scheduled; no agenda details disclosed

Filed 17:13View Source
28 Jul 20261 filing
Board Meeting

Orchid Pharma Board to consider allotment of equity shares under Dhanuka Laboratories amalgamation scheme on Aug 1, 2026

Meeting Details

  • Date: August 01, 2026; time and venue not disclosed.

Key Agenda Items

  • Allotment of Rs 10 equity shares to Dhanuka Laboratories shareholders on record date July 23, 2026 under scheme.

Other Notes

  • Record date July 23, 2026 is noted for the allotment under the scheme.
Filed 18:47View Source
25 Jul 20261 filing
Company UpdateGeneral

Orchid Pharma announces investor roadshow in Singapore with WTD participation on July 29–31, 2026

Investor Roadshow Details

  • Investor roadshow in Singapore to include Orchid Pharma; Mridul Dhanuka to participate as Whole Time Director.
  • Dates: July 29–31, 2026; Meeting type: Group Meet; Mode: Physical.
  • Location: Singapore; Schedule subject to change without prior notice.
  • No unpublished price-sensitive information will be shared during the meet.
  • Regulatory reference: Regulation 30, Schedule III of LODR.
  • Schedule may change due to investor or company exigencies; updated notice will be provided.
  • Issuer: Orchid Pharma Ltd; Scrip code 524372.
Filed 14:52View Source
11 Jul 20261 filing
Company UpdateCertificate under Reg. 74 (5) of SEBI (DP) Regulations, 2018

Reg 74(5) confirmation certificate enclosed for reporting period

Reg 74(5) certificate

  • Confirmation certificate under Reg 74(5) enclosed confirming compliance.
Filed 16:54View Source
Showing 10 of 42 filings