Sun Pharma Announces Complete Acquisition of Taro
Sun Pharmaceutical Industries Ltd. has completed the merger of Taro Pharmaceutical Industries Ltd. with its subsidiary.
Global Pharma | 25/06/2024 | By Aishwarya | 734
Biocon Biologics Gets EMA Approval for Bevacizumab and its New mAbs Facility in India
Biocon Biologics Ltd. has received approval from the European Medicines Agency (EMA) to manufacture biosimilar Bevacizumab at its new, world-class, multi-product monoclonal antibodies (mAbs) drug substance facility in Bengaluru.
Global Pharma | 24/06/2024 | By Aishwarya | 1099
Sun Pharma Signs Non-Exclusive Patent Licensing Deal with Takeda for Vonoprazan
Sun Pharma has entered into a non-exclusive patent licensing agreement with Takeda Pharmaceutical Company Ltd. to commercialise Vonoprazan tablets 10 mg, 20 mg in India under the brand name Voltapraz.
Global Pharma | 24/06/2024 | By Aishwarya | 1146
Lupin Gets EIR from US FDA for its Somerset Manufacturing Facility
Lupin has received the Establishment Inspection Report (EIR) from the United States Food and Drug Administration (US FDA) for its manufacturing facility in Somerset.
Global Pharma | 24/06/2024 | By Aishwarya | 934
argenx Secures FDA Approval for VYVGART Hytrulo Co-Formulated with ENHANZE
Halozyme Therapeutics has announced that argenx has received US Food and Drug Administration (FDA) approval for VYVGART Hytrulo (efgartigimod alfa and hyaluronidase-qvfc) co-formulated with ENHANZE, Halozyme's proprietary recombinant human hyaluronidase enzyme, rHuPH20, for the treatment of adults with chronic inflammatory demyelinating polyneuropathy.
Global Pharma | 24/06/2024 | By Aishwarya | 676
Abzena and Argonaut to Offer End-to-End Drug Development Support for Biopharma Companies
Abzena has inked a strategic partnership with Argonaut Manufacturing Services, Inc. to provide a fully integrated drug substance and drug product manufacturing solution for biopharmaceutical organizations.
Global Pharma | 21/06/2024 | By Aishwarya | 721
Johnson & Johnson Submits Application to US FDA Seeking Approval of TREMFYA
Johnson & Johnson has submitted a supplemental Biologics License Application (sBLA) to the US Food and Drug Administration (FDA) seeking approval of TREMFYA (guselkumab) for the treatment of adults with moderately to severely active Crohn's disease.
Global Pharma | 21/06/2024 | By Aishwarya | 533
Regel Therapeutics Names Stephen J. Farr as New CEO
Regel Therapeutics’ Board of Directors has named Stephen J. Farr, PhD, as the new Chief Executive Officer (CEO).
Global Pharma | 21/06/2024 | By Aishwarya | 378
iOnctura Secures EUR 80 Million in Series B Financing Round
iOnctura, a clinical-stage biopharmaceutical company combating neglected and hard-to-treat cancers, has closed a EUR 80 million Series B financing.
Global Pharma | 21/06/2024 | By Aishwarya | 703
Accuray and TrueNorth Medical Physics Sign Agreement to Provide Radiation Oncology Support
Under the terms of the agreement, TrueNorth Medical Physics will offer services that are complementary and supplementary to those supplied by Accuray, acting as an extension of the hospital team – on-site, remote or hybrid – to help ensure they have the staffing needed to achieve patient treatment goals.
Global Pharma | 20/06/2024 | By Manvi | 449
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