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10 of 54 filings·Updated 28 Sept 2026
Showing 10 of 54 filings.
28 Sept 20261 filing
Insider Trading / SASTClosure of Trading Window

Kwality Pharmaceuticals Ltd: Trading window closed from October 1, 2026 until 48 hours after the declaration of unaudited financial results for the quarter and half-year ended September 30, 2026.

Kwality Pharmaceuticals Ltd: Trading window closed from October 1, 2026 until 48 hours after the declaration of unaudited financial results for the quarter and half-year ended September 30, 2026.

Filed 12:41View Source
2 Sept 20262 filings
Company UpdateChange in Management

Kwality Pharmaceuticals Ltd AGM approves Swanith Kapoor as NED and Aditya Arora as WTD

Director appointments

  • Regularization of Swanith Kapoor as Non-Executive Independent Director; term 02 Jun 2026–01 Jun 2031.
  • Profile: Swanith Kapoor, qualified legal professional with LLB; not related to any director.
  • Aditya Arora re-appointed as Whole Time Director; term 30 Sep 2026–29 Sep 2031; liable to retire by rotation.
  • Profile: Aditya Arora, B.Com; Board since Oct 2015; oversees production, QA, regulatory filings.
  • Relationships: Ajay Kumar Arora (father); Geeta Arora (mother); Ramesh Kumar (paternal uncle); Anju Arora (aunt).
  • Compliance: Not debarred from holding director office.
Filed 23:29View Source
AGM/EGMAGM

AGM outcomes: all six resolutions approved, including director appointments and cost auditor remuneration

AGM details

  • AGM held on 31-08-2026; 12:00–12:35 PM; mode: VC/OAVM.
  • Record date: 24-08-2026; last date for postal ballot receipt: 31-08-2026.
  • Attendees via video conference: 6 promoters, 28 public.
  • All resolutions passed with requisite majority.

Key resolutions

  • Adopt standalone and consolidated financial statements for year ended Mar 31, 2026.
  • Re-appoint Aditya Arora as Director by rotation.
  • Re-appoint Anju Arora as Director by rotation.
  • Appointment of Independent Director Kapoor.
  • Re-appoint Aditya Arora as Whole-time Director; remuneration approved.
  • Ratify Cost Auditors' remuneration.

Voting results

  • Resolution 1: passed with near-unanimous support.
  • Resolution 2: passed with high approval; minor opposition.
  • Resolution 3: passed with high approval; minimal dissent.
  • Resolution 4: passed with strong majority; some against.
  • Resolution 5: passed with strong majority; small opposition.
  • Resolution 6: passed with near-unanimous support; negligible dissent.
Filed 23:12View Source
31 Aug 20261 filing
AGM/EGMAGM

Kwality Pharmaceuticals 43rd AGM via VC/OAVM approves financials, director re-appointments, Independent Director, and cost auditor remuneration

AGM Details

  • Date and time: 31 August 2026, 12:00 IST.
  • Mode: VC/OAVM at the registered office (deemed venue).
  • Quorum: 34 members attended.

Key Resolutions

  • Ordinary: Adopt standalone and consolidated financial statements for FY2025-26.
  • Ordinary: Re-appoint Aditya Arora as Director (retiring by rotation).
  • Ordinary: Re-appoint Anju Arora as Director (retiring by rotation).
  • Special: Appoint Swanith Kapoor as Independent Director.
  • Special: Re-appoint Aditya Arora as Whole Time Director; remuneration approved.
  • Ordinary: Ratify Cost Auditors' remuneration.

Voting Status

  • Voting results pending; Scrutinizer's report to be submitted separately.

Director Changes

  • Swanith Kapoor appointed as Independent Director.
  • Aditya Arora re-appointed as Director (rotating) and Whole Time Director; remuneration to be approved.
  • Anju Arora re-appointed as Director (rotating).

Auditor Matters

  • Cost Auditors remuneration ratified; tenure details not disclosed.
Filed 18:27View Source
13 Aug 20261 filing
Company UpdateNewspaper Publication

Newspaper Publication of Unaudited Financial Results for the quarter ended June 30, 2026.

No brief for this announcement.Newspaper publications aren’t summarised. View the original using the link below
Filed 16:44View Source
12 Aug 20263 filings
Company UpdateNewspaper Publication

Newspaper Publication of Notice of 43rd Annual General Meeting.

No brief for this announcement.Newspaper publications aren’t summarised. View the original using the link below
Filed 18:24View Source
Company UpdateAnalyst / Investor Meet

Kwality Pharmaceuticals held virtual investors meeting on 10 August 2026 organized by Go India Advisors

Meeting Details

  • Date and Time: 10 August 2026, 4:00 PM IST.
  • Type and mode: Knowledge Session (Virtual Interaction) for Investors.
  • Organiser: Go India Advisors on behalf of Kwality Pharmaceuticals.
  • Participants: Company management (roles not specified) presented.
  • Purpose: discuss operations, performance, outlook; no UPSI shared.
  • Recording: audio/video recording available; access link provided.
Filed 15:49View Source
Company UpdateEarnings Call Transcript

Kwality Pharmaceuticals Q1 FY27 earnings call: BE filings, biologics/hormones ramp, and 2030 revenue target; KPMG auditor appointment

Operating Update

  • Sixth unit (hormone) to commence by November 2026.
  • Oncology share forecast 25-30% in FY27 due to registrations delays.
  • Unit 5 biologicals: Erythropoietin BE pre-clinical complete; trials to start by Nov/Dec 2026.
  • ROW registrations targeted in 10-12 geographies; Indian sales immediate.
  • Portfolio targets 200-250 products; filings across 60-80 countries; per registration INR 1.5-2.0 million.

Guidance and Outlook

  • FY27 revenue expected to cross INR 700-720 crore.
  • FY28 EBITDA around 30% at INR1,000 crore revenue.
  • FY29 EBITDA target around 30%.
  • FY30 revenue target INR1,500 crore; growth 25-30% CAGR.
  • FY29 guidance excludes biological and hormone; potential contributions in FY30.

Capex and Projects

  • Bio facility: 100L CDSCO approved; 500L installed; CDSCO approval pending.
  • BE programs: Ampho B liposomal and Octreotide to finish by Apr-May FY28.
  • Leuprolide 45 mg first generic in 75-80% markets; submission by FY28 Q2.
  • Algeria biosimilar JV: fill-finish plant; Kwality provides technology; data generation parallel.
  • Biosimilar capex: INR150 crores; spend FY28 Q3 to FY29 Q4.

Auditor and Governance

  • KPMG to audit; appointment expected by FY27 end.
  • Q3/Q4 FY27 appointment aligns with call remarks.

Q&A Highlights

  • Biological/hormone not in FY29 guidance; potential in FY30.
  • BE filings expected to yield six to seven registrations per quarter.
  • FY30 revenue mix: general facility about 40%; LATAM 30-35%; Europe 10-15%.
  • Margins may be higher than 30% beyond FY29.
Filed 15:33View Source
10 Aug 20262 filings
Company UpdateInvestor Presentation

Kwality Pharmaceuticals raises FY27 revenue guidance to 700+ Cr with EBITDA 27–28% and BE/Regulated market expansion.

Business Overview

  • Core business: injectables, beta-lactams, and complex molecules.
  • In-house DSIR-recognized R&D; expanding biologics and hormone capabilities.
  • Exports to 70+ markets; diversified global manufacturing and regulatory readiness.

Key Operational Highlights

  • FY26 revenue was INR 503 Cr; FY27 guidance raised to 700+ Cr.
  • EBITDA margin FY26 about 23.5%; FY27 guidance 27–28%.
  • PAT margin FY26 about 13.4%; FY27 target ~15.5%+.
  • Hormone Unit 6 capex planned at INR 65 Cr; ~50% incurred.
  • First biologic Erythropoietin planned in H1 FY28.
  • EU-GMP readiness: 4 of 5 plants approved; expanded regulated access.
  • BE programs: 40+ solid-dose BE programs; 3+ BE studies completed in quarter.
  • Working capital cycle reduced from 297 to 161 days.
  • R&D headcount: 80 scientists; DSIR-recognized.
  • Unit 6: hormone facility under construction; 4 of 5 units EU-GMP approved.

Financial Performance

  • FY26 revenue: INR 503 Cr; FY27 guidance: 700+ Cr.
  • FY26 EBITDA margin: ~23.5%; FY27 target: 27–28%.
  • FY26 PAT margin: ~13.4%; FY27 target: ~15.5%+.
  • Q1FY27 revenue: INR 162.4 Cr.
  • Cash conversion cycle improved to 161 days; strong cash flow.
  • Balance sheet: low leverage with healthy debt/coverage; capex headroom.

Capital Structure & Liquidity

  • Low leverage and strong coverage; substantial headroom for capex.
  • Working capital discipline driving cash generation.
  • Export activities with long-cycle receivables managed through scale.

Strategic Priorities & Outlook

  • Capex-led expansion across oncology, biologics, and hormones.
  • Commercialize first biologic, Erythropoietin, in H1 FY28.
  • EU-GMP readiness to unlock regulated markets; 4/5 plants approved.
  • Licensing-driven exports to LATAM, Africa, MENA; 70+ markets.
  • R&D pipeline: BE optimization and high-margin niche formulations.

Risks & Mitigation

  • Regulatory approvals required; EU-GMP readiness ongoing.
  • Capex execution risk; strength of balance sheet provides headroom.
  • BE program outcomes critical for sustained growth.

Governance & Leadership

  • Chairman & MD: Ramesh Arora; Directors: Ajay Arora, Aditya Arora.
  • DSIR-recognized in-house R&D; centralized QA/QC across units.
  • Audits: 20+ regulatory, customer, and vendor audits completed.
Filed 12:40View Source
Board MeetingOutcome of Board Meeting

Kwality Pharmaceuticals approves Q1 FY27 standalone and consolidated unaudited results; raises FY27 guidance

Board approvals

  • Standalone and consolidated unaudited Q1 FY27 results approved; quarter ended 30 June 2026.
  • Board approved results after Audit Committee review on 10 August 2026.
  • Auditors' limited review reports submitted; auditors did not express an audit opinion.

Financial results and guidance

  • Consolidated revenue grew 46% YoY to ₹162 crore; EBITDA ₹41 crore; PAT ₹26 crore.
  • FY27 guidance raised: revenue ₹700+ crore, EBITDA ₹189-196 crore, PAT ₹109+ crore.

R&D and regulatory updates

  • R&D progress: 13 BE studies completed; 15+ BE filings; 15+ product registrations across select markets.
  • Biologics: Pembrolizumab pre-clinical batches approved; Erythropoietin progressed to clinical trial.
  • Hormone facility on schedule; completion targeted November 2026.
  • Regulatory footprint expanded across PIC/S regulators including ANVISA, SFDA, INVIMA, DIGEMID, EU-GMP.

Audit and reporting notes

  • Limited audit review; results prepared under Ind AS 34 and Regulation 33 requirements.
Filed 12:09View Source
Showing 10 of 54 filings