If the document you are looking for isn’t listed above, give us a call. All documents produced by Pearl Pathways undergo thorough statistical, editorial, scientific, and quality control review. We use our extensive scope of knowledge working with the life sciences industry, academia, and clinical research organizations to guide you through your project. Pearl Pathways’ medical writers become part of your team and are mindful of your project needs. Product Website Content (both scientific and patient audiences).Standard Operating Procedures (SOPs) Covering all Aspects of Drug Development.Editorial support/Journal/Conference Submission.Preclinical and Clinical Reports and Summaries.ADME, Pharmacokinetic, Pharmacodynamic, Toxicology Analysis.Conference Materials (abstracts, poster presentations and slide sets).IND, IDE, BLA, NDA, ANDA, Clinical and non-Clinical Sections of the Common Technical Document (CTD).Protocols, Informed Consent Documents, and Patient Brochures.Professional medical writing is an ethical service that can enhance the. Pearl Pathways’ medical writing services include clinical and regulatory writing, as well as scientific communications, education materials, and medical writing consultancy. The value that a PMW brings to the manuscript. Our skilled medical writers bring a deep understanding of publication strategy to support manuscript writing, making them more than just good writers. Documentation that meets the utmost ethical and scientific standards is the end goal for all of our medical writers. Our medical writers work closely with project management, pharmacovigilance, statistical, regulatory and clinical data management teams to deliver accurate documentation and strong story telling. We understand the difference! Medical writing is an integral part of regulatory compliance and clinical research. The difference between good writing and good medical writing cannot be overstated.
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