Accelerate your drug development by leveraging QCP principles and Model-informed drug development (MIDD). Our experienced team offers strategic guidance on clinical strategy and the design, execution, analysis, and reporting of clinical pharmacology studies.
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Achieve better decision-making, minimise risk and reduce development costs with our MIDD services. We leverage quantitative clinical pharmacology to optimise drug development strategies and support regulatory submissions.
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MBPharmaco Consulting offers expert clinical pharmacology regulatory writing assistance for NDA/BLA regulatory submissions (2.7.1 & 2.7.2) on a global scale. Our team collaborates closely with clinical pharmacology teams, ensuring the timely delivery of high-quality documents.
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We offer exceptional scientific and technical writing services that cater to a broad range of areas and document types. Our team of experienced writers possesses a comprehensive understanding of terminology and jargon, relevant guidelines and excellent writing skills, enabling them to create documents that effectively communicate complex scientific information to the intended audience. Our writers […]
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