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Dr. Divya Colin
Dr. Divya Colin

    Doctor of Pharmacy

    Dr. Divya Colin, a Doctor of Pharmacy Graduate with extensive experience in clinical and hospital settings and confidently equipped with diagnostic and therapeutic skills. She also has spread out exposure to Oncology Departments in Mysore Medical College and Research Institute as Oncology Pharmacist. Currently she is building a career in clinical research and clinical data management. She has been a part of Medical Dialogue since January 2022.

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    Articles By : Dr. Divya Colin

    Akum Pharma Asked to Submit Safety Data for Alzheimers Drug Combo In Elderly Indian Patients

    Akum Pharma Asked to Submit Safety Data for Alzheimer's Drug Combo In Elderly Indian Patients

    Dr. Divya Colin5 Aug 2025 5:31 PM IST
    New Delhi: In a recent regulatory review, the Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO)...
    MSN Labs Gets CDSCO Panel Nod to Begin Phase III Trial of Cenobamate Tablets, With Safety Caveat

    MSN Labs Gets CDSCO Panel Nod to Begin Phase III Trial of Cenobamate Tablets, With Safety Caveat

    Dr. Divya Colin5 Aug 2025 4:15 PM IST
    New Delhi: Considering the bioequivalence study results of the MSN Labs Cenobamate Tablets 12.5 mg, 25 mg, 50mg, 100 mg, 150 mg & 200 mg, the...
    Setback To Novartis: CDSCO Panel Rejects Lanalumab Phase III Trial Design Over Study Flaws

    Setback To Novartis: CDSCO Panel Rejects Lanalumab Phase III Trial Design Over Study Flaws

    Dr. Divya Colin4 Aug 2025 6:00 PM IST
    New Delhi: In a setback to Novartis, the Subject Expert Committee (SEC) under the Central Drugs Standard Control Organisation (CDSCO) has declined to...
    CDSCO Panel Recommends Approval for Vorasidenib with Phase-III Waiver, Mandates Phase-IV Trial in India

    CDSCO Panel Recommends Approval for Vorasidenib with Phase-III Waiver, Mandates Phase-IV Trial in India

    Dr. Divya Colin3 Aug 2025 12:00 PM IST
    New Delhi: In response to a proposal by Servier India Pvt. Ltd. seeking approval to import and market the anti-cancer drug Vorasidenib Tablets 10 mg...
    Veeda Clinical Research Gets Expert Committee Nod To Conduct BA/BE Study Of Ibrutinib For Export

    Veeda Clinical Research Gets Expert Committee Nod To Conduct BA/BE Study Of Ibrutinib For Export

    Dr. Divya Colin1 Aug 2025 9:45 AM IST
    New Delhi: Veeda Clinical Research Limited got approval from the Subject Expert Committee (SEC) functional under the Central Drug Standard Control...
    18 Medical Device Firms Got Rs 133.95 Cr in Incentives Till FY2024-25: Govt Tells RS

    18 Medical Device Firms Got Rs 133.95 Cr in Incentives Till FY2024-25: Govt Tells RS

    Dr. Divya Colin31 July 2025 1:00 PM IST
    New Delhi: A total of 18 domestic medical device manufacturers have received Rs 133.95 crore in incentives under the Production Linked Incentive (PLI)...
    NPPA Regulated Prices of 2,295 Essential Drugs Over Five Years, Says Govt

    NPPA Regulated Prices of 2,295 Essential Drugs Over Five Years, Says Govt

    Dr. Divya Colin30 July 2025 4:12 PM IST
    New Delhi: In a move to enhance affordability and ensure price regulation of essential medicines, the Government of India has confirmed that the...
    Troikaas Fast-Acting Paracetamol Shot Hits Regulatory Hurdle, CDSCO Panel Seeks More Data

    Troikaa's Fast-Acting Paracetamol Shot Hits Regulatory Hurdle, CDSCO Panel Seeks More Data

    Dr. Divya Colin27 July 2025 3:00 PM IST
    New Delhi: The Subject Expert Committee (SEC) under the Central Drugs Standard Control Organisation (CDSCO) has asked Troikaa Pharmaceuticals Ltd. to...
    India Cuts API Imports, Disburses Rs 1,008 Cr Under PLI Schemes, Parliament Told

    India Cuts API Imports, Disburses Rs 1,008 Cr Under PLI Schemes, Parliament Told

    Dr. Divya Colin26 July 2025 8:02 PM IST
    New Delhi: India has disbursed over Rs 1,008 crore in incentives to domestic firms to bolster Active Pharmaceutical Ingredient (API) production,...
    Cipla Bommasandra facility gets VAI classification from USFDA

    CDSCO Panel Clears Cipla's Glycopyrronium-Formoterol Inhaler for Phase IV Trial

    Dr. Divya Colin23 July 2025 5:00 PM IST
    New Delhi: The Subject Expert Committee (SEC) under the Central Drugs Standard Control Organisation (CDSCO) has granted Cipla Limited approval to...
    Zydus Asked to Revise Phase III Trial Protocol for Cough Syrup FDC After CDSCO Panel Review

    Zydus Asked to Revise Phase III Trial Protocol for Cough Syrup FDC After CDSCO Panel Review

    Dr. Divya Colin18 July 2025 9:52 PM IST
    New Delhi: The Subject Expert Committee (SEC) under the Central Drugs Standard Control Organisation (CDSCO) has recommended key revisions to the Phase...
    Pfizer Gets CDSCO Panel Nod To Conduct Phase III Trial of RSV Vaccine in India, Told to Clarify Subject Criteria

    Pfizer Gets CDSCO Panel Nod To Conduct Phase III Trial of RSV Vaccine in India, Told to Clarify Subject Criteria

    Dr. Divya Colin13 July 2025 1:00 PM IST
    New Delhi: Pfizer has received approval from the Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation...
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