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    Pharma News

    India: Dr. Reddy's Gets 4 Observations from USFDA for Telangana Plant

    India: Dr. Reddy's Gets 4 Observations from USFDA for Telangana Plant

    Dr. Reddy’s Laboratories has said that the US health regulator had issued four observations after inspecting its active pharmaceutical ingredients (API) facility in Telangana. “The audit of our API Hyderabad plant 1 at Jinnaram Mandal, Medak district...
    US India FDA

    2018-04-08

    India: Dr. Reddy's Foundation to Help Girls Taking up Science Careers

    India: Dr. Reddy's Foundation to Help Girls Taking up Science Careers

    The criteria for selection will be good academic record and admission into 12 recognised colleges identified by DRF for the present.
    DRF India People

    2018-04-08

    India: CDSCO Mulls Forum for Interacting with Pharma Industry on Regulations

    India: CDSCO Mulls Forum for Interacting with Pharma Industry on Regulations

    The Central Drugs Standard Control Organisation (CDSCO) has decided to constitute a forum for its chief to meet pharma associations regularly as part of efforts to improve ease of doing business for the country’s pharmaceutical industry.
    CDSCO India

    2018-04-08

    India: Pharma Exports from Visakhapatnam Set to Become Hassle-Free

    India: Pharma Exports from Visakhapatnam Set to Become Hassle-Free

    Export of drug and pharmaceuticals from Visakhapatnam sea port and airport is set to become smoother. To facilitate exports, a team of officials, including an assistant drug controller (ADC), drug inspector and an assistant drug inspector, has been...
    India: States Must Recall Drugs, Combination Medicines Sold Without DCGI Nod

    India: States Must Recall Drugs, Combination Medicines Sold Without DCGI Nod

    In an effort to close the tap on new drugs and combination medicines entering the market without regulatory approval, the Drug Controller General of India (DCGI) is writing to State regulators to review and recall such medicines already in the market.
    India Pharmaceutical

    2018-04-08

    Rhythm, Takeda Enter Development Agreement

    Rhythm, Takeda Enter Development Agreement

    Rhythm Pharmaceuticals has acquired exclusive, worldwide rights from Takeda to develop and commercialize T-3525770 (now RM-853).
    Therapure Biopharma Launches Biologics Division

    Therapure Biopharma Launches Biologics Division

    Therapure Biopharma has launched its plasma products and technology division as Evolve Biologics. Evolve's leadership team consists of chief executive officer Blaine Forshage; chief commercial officer, David Holliday; and chief financial officer...
    FujiFilm Acquires Irvine Scientific from JXTG

    FujiFilm Acquires Irvine Scientific from JXTG

    JXTG Nippon Oil & Energy Corporation has announced it has agreed to sell Irvine Scientific Sales Company, Inc. and IS Japan Co., Ltd. to FUJIFILM Corporation (FujiFilm).
    R&D acquisition FujiFilm

    2018-04-04

    AstraZeneca, Compugen in $200M Drug Discovery Tie-up

    AstraZeneca, Compugen in $200M Drug Discovery Tie-up

    Compugen, a provider of predictive discovery and development of first-in-class therapeutics for cancer immunotherapy, has entered into an exclusive license agreement with MedImmune (www.medimmune.com), the global biologics research and development arm...
    C4X, Indivior Sign License Agreement

    C4X, Indivior Sign License Agreement

    C4X Discovery has signed a licensing agreement with Indivior to further develop and commercialize C4XD's oral Orexin-1 receptor antagonist ("C4X3256") for the treatment of addiction.
    EC Approves Alofisel For Complex Perianal Fistulae In Crohn’s Disease

    EC Approves Alofisel For Complex Perianal Fistulae In Crohn’s Disease

    TiGenix NV and Takeda Pharmaceutical Company have announced that the European Commission (EC) has approved Alofisel (darvadstrocel), previously Cx601, for the treatment of complex perianal fistulae in adult patients with nonactive/mildly active ...
    Takeda disease TiGenix

    2018-04-04

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