DS Inpharmatics

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Leading the Charge in Comprehensive Drug Development Solutions

Specializing in the intricate field of drug information, this company is a leading provider of comprehensive regulatory, technical, and project management consulting services. The organization collaborates with healthcare product companies focusing on the manufacture and marketing of pharmaceuticals, biopharmaceuticals, and gene therapy products. Noted for its innovative strategies since its inception in 2007, the firm offers a full spectrum of expertise that spans the entire drug development process, including strategic planning, meticulous regulatory submissions, and stringent compliance management. By focusing on chemistry, manufacturing, and controls (CMC) aspects, the company excels in creating robust development programs tailored to optimize product approval processes and mitigate regulatory challenges.

Following its recent acquisition by a global leader in the life sciences regulatory sector, the organization has expanded its ability to provide clients with an enhanced breadth of specialist knowledge and international capabilities. The team of seasoned professionals, many with over a decade of industry experience, is committed to accelerating clients' project timelines by offering decisive guidance and hands-on support encompassing every development stage. This includes advising on product manufacturing, regulatory strategies, and interactions with regulatory bodies to ensure successful marketing applications for diverse therapeutic areas. Through its dedication to precision and efficiency, the firm continues to solidify its reputation as a pivotal partner in the drug information industry, ensuring products achieve regulatory success while adhering to the highest standards of quality and safety.

Leading the Charge in Comprehensive Drug Development Solutions

Specializing in the intricate field of drug information, this company is a leading provider of comprehensive regulatory, technical, and project management consulting services. The organization collaborates with healthcare product companies focusing on the manufacture and marketing of pharmaceuticals, biopharmaceuticals, and gene therapy products. Noted for its innovative strategies since its inception in 2007, the firm offers a full spectrum of expertise that spans the entire drug development process, including strategic planning, meticulous regulatory submissions, and stringent compliance management. By focusing on chemistry, manufacturing, and controls (CMC) aspects, the company excels in creating robust development programs tailored to optimize product approval processes and mitigate regulatory challenges.

Following its recent acquisition by a global leader in the life sciences regulatory sector, the organization has expanded its ability to provide clients with an enhanced breadth of specialist knowledge and international capabilities. The team of seasoned professionals, many with over a decade of industry experience, is committed to accelerating clients' project timelines by offering decisive guidance and hands-on support encompassing every development stage. This includes advising on product manufacturing, regulatory strategies, and interactions with regulatory bodies to ensure successful marketing applications for diverse therapeutic areas. Through its dedication to precision and efficiency, the firm continues to solidify its reputation as a pivotal partner in the drug information industry, ensuring products achieve regulatory success while adhering to the highest standards of quality and safety.

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