Unlock Excellence in Scientific Writing
Looking for high-quality, end-to-end scientific writing with swift turnaround times? Our expert team, with cross-domain expertise, ensures precise, compliant, and impactful documents for regulatory submissions and beyond.
Let’s elevate your submissions. Discover our expertise today!
We are your teammates on the path to process validation. Our experts in clinical, regulatory, and technical writing help build the foundation for a strong dossier. We also support literature searches, meeting reports, and translations. We guarantee high quality and quick turnaround times.
At Akkodis, we specialize in clear, precise, and effective scientific writing to support clinical research and ensure regulatory compliance. Our team consists of international consultants and freelance experts in clinical, regulatory, and technical writing, ready to assist you in achieving successful research outcomes.
We bring in-depth knowledge across various therapeutic areas, including vaccines, pharmaceuticals, oncology, and consumer healthcare. From pre-clinical to post-marketing study phases, our expertise ensures high-quality study-related documentation.
Our team has long-standing experience in regulatory writing, supporting accelerated submissions to major health authorities like the FDA, EMA, JNDA, NMPA, and EEU. We ensure full alignment with ICH-GCP and the latest regulatory standards, delivering documents essential for clinical approvals.
We provide customized writing and project management support, including coaching, process standardization, and stakeholder engagement. Our team delivers a wide range of critical study and regulatory documents with swift turnaround times.
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