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Author: Firma WELDING

WELDING GmbH & Co. KG, through its business unit PHARMA FDF, announces its first European marketing authorizations for Tafamidis 61 mg soft capsules

Posted on 29. May 2026 by Firma WELDING Posted in General Tagged biosimilar development, Decentralized Procedure, drug registration, EMA approval, generic medication, international pharma market, market authorization, marketing authorizations, multi country generic approval, pharmaceutical licensing, regulatory expertise, regulatory pathway, supply resilience, Tafamidis 61 mg soft capsules, value-based partnerships

WELDING GmbH & Co. KG announces an important regulatory milestone in Europe. Following the successful closure of the Decentralized Procedure (DCP) earlier this year, WELDING GmbH & Co. KG in collaboration with its partner Zenara Pharma Pvt Ltd has received its […]

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WELDING GmbH & Co. KG Expands to Latin America

Posted on 27. May 2026 by Firma WELDING Posted in General Tagged Active Pharmaceutical Ingredients, competitive pricing, distribution expertise, Food Additives, functional nutrition, ingredient sourcing, international subsidiary, Latin American market, manufacturing standards, market expansion, mexico, pharmaceutical distribution, Regulatory Compliance, supply chain resilience, traceability systems

WELDING GmbH & Co. KG announces the establishment of its Mexican subsidiary, WELDING Ingredientes SA de CV. With this step, our family-owned company is expanding its international presence and strengthening its position in the Latin American market. Our goal is […]

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Revio Therapeutics and Welding Group Announce Strategic Co-Development and Licensing Agreement for Innovative Specialty Oncology Product

Posted on 24. March 202624. March 2026 by Firma WELDING Posted in General Tagged biotechnology, cancer, drug development, healthcare innovation, market access, oncology, partnership, patient care, Regulatory Compliance, Revio, specialty pharmaceuticals, therapeutics

Revio Therapeutics ("Revio") and Welding Group ("Welding") today announced the signing of a co-development and licensing agreement for Revio’s proprietary specialty oncology product. The 505(b)(2) product, designed based on an innovative dosage form with significant patient compliance and ease-of-use advantages, will be developed […]

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