Scientific and medical writing services, ranging from nonclinical, peer-reviewed manuscripts to regulatory submissions and clinical documents
Intertek’s medical and pharmaceutical experts have diverse scientific knowledge and extensive experience of pharmaceutical development to produce clear and concisely worded documents for medical and pharmaceutical companies worldwide. Based on our industry experience and regulatory interactions, we are able to prepare a diverse range of medical and pharmaceutical documentation to address the needs of various stakeholders, including clinical investigators, IRBs, medical monitors, study coordinators and regulatory reviewers.
Intertek can assist your company with all nonclinical and clinical Associated Regulatory Tasks including:
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