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WACKER & CordenPharma Enter Pandemic Readiness State for Germany

WACKER & CordenPharma Enter Pandemic Readiness State for Germany

WACKER and CordenPharma have officially entered the pandemic readiness state as of June 1, 2024.

| 25/06/2024 | By 377

ANI Pharmaceuticals to Acquire Alimera to Expand Rare Disease

ANI Pharmaceuticals to Acquire Alimera to Expand Rare Disease

ANI Pharmaceuticals, Inc. has announced that ANI will acquire Alimera for USD 5.50 per share in cash at closing and one non-tradable contingent value right (CVR) representing the right to receive up to USD 0.50 per share upon the achievement of certain net revenue targets in 2026 and 2027.

| 25/06/2024 | By 830

Sun Pharma Announces Complete Acquisition of Taro

Sun Pharma Announces Complete Acquisition of Taro

Sun Pharmaceutical Industries Ltd. has completed the merger of Taro Pharmaceutical Industries Ltd. with its subsidiary.

| 25/06/2024 | By 829

Biocon Biologics Gets EMA Approval for Bevacizumab and its New mAbs Facility in India

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.

| 24/06/2024 | By 1238

Sun Pharma Signs Non-Exclusive Patent Licensing Deal with Takeda for Vonoprazan

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.

| 24/06/2024 | By 1311

Lupin Gets EIR from US FDA for its Somerset Manufacturing Facility

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.

| 24/06/2024 | By 981

argenx Secures FDA Approval for VYVGART Hytrulo Co-Formulated with ENHANZE

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.

| 24/06/2024 | By 726

Bora to Acquire Emergent Sterile Manufacturing Facility in Maryland

Bora to Acquire Emergent Sterile Manufacturing Facility in Maryland

Bora Pharmaceuticals has signed an agreement for Emergent BioSolutions' sterile manufacturing facility in Baltimore-Camden, Maryland as part of a major commercial expansion for the company.

| 21/06/2024 | By 567

Abzena and Argonaut to Offer End-to-End Drug Development Support for Biopharma Companies

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.

| 21/06/2024 | By 776

Johnson & Johnson Submits Application to US FDA Seeking Approval of TREMFYA

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.

| 21/06/2024 | By 558

 
 

 

 

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