Our regulatory writers are experts at meeting global regulatory requirements and adhering to guidance documents, such as International Council for Harmonisation Good Clinical Practice guidelines. Our team are highly skilled at conveying complex scientific and clinical information in a clear, concise, and accurate manner, all while adhering to strict timelines and collaborating with cross-functional teams. Most of our regulatory writers hold a PhD in a science-related field and have many years of experience in writing and managing regulatory documents throughout the entire drug development journey.
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At Alchemy, we understand the critical role of medical education in enhancing the knowledge and skills of healthcare professionals and the ultimate impact of this on patients’ lives. Our dedicated team of medical writers are committed to developing high-quality materials that meet the evolving needs of patients and the medical community. We work on a range of both promotional and non-promotional assets that empower healthcare professionals to stay abreast of the latest advancements in their fields.
At Alchemy, we understand that good publications are essential to disseminate key findings to target audiences and bring attention to a company’s work and brand. Our team offers support across the entire publications journey, producing clear, compliant, and accurate deliverables. From target journal research to responding to peer review comments; we’ve got you covered. Our writers are trained in Good Publication Practices and ICMJE recommendations, and a growing number are Certified Medical Publication Professionals™ (CMPP™).
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Preclinical publications, clinical trial manuscripts, case reports, observational studies and literature reviews
Starting at kick-off and ending at submission of the final proof
Data checking, formatting, referencing, ensuring compliance with journal guidelines
Trained in ICMJE, GPP, CONSORT and STROBE guidelines
Our writers provide comprehensive referencing and editing support tailored to your style.
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