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Parthika Patel
Parthika Patel

    M. Pharm (Pharmaceutics)

    Parthika Patel has completed her Graduated B.Pharm from SSR COLLEGE OF PHARMACY and done M.Pharm in Pharmaceutics. She can be contacted at editorial@medicaldialogues.in. Contact no. 011-43720751

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    • Parthika Patel

    Articles By : Parthika Patel

    CDSCO Cancels Import Licence of Mediderma Salipeel Products

    CDSCO Cancels Cosmetic Import Registration of Indian Agent for Proteos Biotech

    Parthika Patel11 Aug 2025 3:45 PM IST
    New Delhi: The Central Drugs Standard Control Organisation (CDSCO) has cancelled the Cosmetic Registration Certificate No. RC/COS-003595, held by NKG...
    CDSCO Panel Accepts Glenmarks Apremilast Trial Report, Seeks 2-Year PSUR Data

    CDSCO Panel Accepts Glenmark's Apremilast Trial Report, Seeks 2-Year PSUR Data

    Parthika Patel10 Aug 2025 1:00 PM IST
    New Delhi: Glenmark Pharmaceuticals Limited has received approval from the Subject Expert Committee (SEC), functioning under the Central Drugs...
    Intas Pharma Gets Expert Panel Nod For PMS Data On Tofacitinib Ointment In Atopic Dermatitis

    Intas Pharma Gets Expert Panel Nod For PMS Data On Tofacitinib Ointment In Atopic Dermatitis

    Parthika Patel9 Aug 2025 11:30 AM IST
    New Delhi: Intas Pharma has received approval from the Subject Expert Committee (SEC) under the Central Drugs Standard Control Organisation (CDSCO)...
    Abbott to Conduct BE Study for Carbimazole 15 mg, Trial Waiver Granted In India

    Abbott to Conduct BE Study for Carbimazole 15 mg, Trial Waiver Granted In India

    Parthika Patel8 Aug 2025 2:34 PM IST
    New Delhi: Abbott Healthcare Pvt. Ltd has received the green signal from the Subject Expert Committee (SEC) under the Central Drugs Standard Control...
    Dr Reddys Gets CDSCO Panel Approval To Begin Phase III Trial of Tapinarof Cream

    Dr Reddy's Gets CDSCO Panel Approval To Begin Phase III Trial of Tapinarof Cream

    Parthika Patel7 Aug 2025 11:41 PM IST
    New Delhi: Dr. Reddy's Laboratories Limited has received approval from the Subject Expert Committee (SEC) under CDSCO to conduct a Phase III clinical...
    No Waiver for Faricimab: CDSCO Panel Asks Roche to Conduct Phase III Trial in India

    No Waiver for Faricimab: CDSCO Panel Asks Roche to Conduct Phase III Trial in India

    Parthika Patel6 Aug 2025 3:34 PM IST
    New Delhi: Roche Products (India) Pvt Ltd has been directed by the Subject Expert Committee (SEC) of the Central Drugs Standard Control Organisation...
    Novartis Told to Revise Protocol, Justify Sample Size in ITU512 Clinical Trial Proposal

    Novartis Told to Revise Protocol, Justify Sample Size in ITU512 Clinical Trial Proposal

    Parthika Patel3 Aug 2025 9:30 AM IST
    New Delhi: Novartis Healthcare Private Limited has been directed by the Subject Expert Committee (SEC) functional under the Central Drugs Standard...
    Biodeal Told To Justify Novel Delivery Claim In NPPA Exemption Plea For Midazolam Nasal Spray

    Biodeal Told To Justify Novel Delivery Claim In NPPA Exemption Plea For Midazolam Nasal Spray

    Parthika Patel2 Aug 2025 4:51 PM IST
    New Delhi: Biodeal Pharmaceuticals Limited has been directed by the National Pharmaceutical Pricing Authority (NPPA) to submit documents supporting...
    Intas Pharma Gets Expert Panel Nod For PMS Data On Tofacitinib Ointment In Atopic Dermatitis

    CDSCO Panel Accepts Phase I Trial Data for Intas' Denosumab Biosimilar

    Parthika Patel2 Aug 2025 4:40 PM IST
    New Delhi: The Subject Expert Committee (SEC) under the Analgesic and Rheumatology division of the Central Drugs Standard Control Organisation (CDSCO)...
    Submit BE Raw Data, Interaction Study on Dapagliflozin-Rosuvastatin FDC: Expert Panel Tells Pure and Cure

    CDSCO Panel Clears PURE & CURE's Sickle Cell Trial With Conditions On Sample Size, Sites

    Parthika Patel1 Aug 2025 5:09 PM IST
    New Delhi: PURE & CURE Healthcare Pvt. Ltd. has received a recommendation from the Subject Expert Committee (SEC) under the Central Drugs Standard...
    CDSCO Panel Withholds Nod for Syngenes Pegfilgrastim Trial, Seeks Additional Data

    CDSCO Panel Withholds Nod for Syngene's Pegfilgrastim Trial, Seeks Additional Data

    Parthika Patel31 July 2025 2:01 PM IST
    New Delhi: The Subject Expert Committee under the Central Drugs Standard Control Organisation (CDSCO) has directed Syngene International Limited to...
    Zydus Told To Conduct Phase III Trial in India for Lurbinectedin Injection, BE Study Waived

    Zydus Told To Conduct Phase III Trial in India for Lurbinectedin Injection, BE Study Waived

    Parthika Patel31 July 2025 1:49 PM IST
    New Delhi: Zydus Lifesciences Limited has been directed to conduct a Phase III clinical trial in the Indian population for its proposed oncology drug...
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