Thought Leadership Many of our medical writing associates and members of our leadership team are active speakers and participants in forums within the medical writing community, including national and chapter conferences of the Drug Information Association, Drug Information Association Medical Affairs and Scientific Communication, American Medical Affairs and Scientific Communication, and American Medical Writers Association, as well as internal customer summits.
Recent topics presented by our writers have included: In addition to providing support on an individual clinical trial or project basis, we have extensive experience in building functional service provider relationships (FSPs), offering collaborative and strategic solutions that provide layers of additional benefit to our customers.
The Freyr medical writing team has proven proficiency in developing and delivering world-class Regulatory medical and scientific writing services for its growing clientele of (global large) Pharma, leading CROs and other Biotech companies adhering to stringent timelines and high-quality parameters.
Freyr also ensures that the writing is in line with the corresponding clinical research.
PPD offers a comprehensive suite of medical writing services to support your clinical trial documentation needs from the early phases of development through post-approval. All documents are prepared on time and are scientifically sound and fully compliant with any applicable regulatory guidelines.So, the current scenario in the clinical research industry is, every organisation leers for a befitting services to enhance its clinical study documentation requirements through best medical writing services across the globe.Our A-Z team of zealous medical writers is ingenious across regulatory medical writing and all therapeutic areas as well as hot segments like recombinant products.Medpace’s integrated team helps plan and coordinate each aspect of regulatory strategy and engagement, balancing strategy, data, analysis, and timelines by globally optimizing regulatory interactions and strategic approaches. Please be aware that if you continue browsing the website without changing your cookie settings, you consent to this. and master’s level writers with diverse therapeutic backgrounds who can support preparation of a wide range of medical communication materials, including: Our medical writers prepare clear, well-written documents designed to exceed expectations in terms of both content and formatting.Writers undergo regular training conducted by the EMWA (European Medical Writers Association), the AMWA (American Medical Writers Association) and other recognized medical writing organisations to keep their skills at the vanguard of the medical-writing field.Felicitous and competent documentation is vital for the success of clinical development program.As well as providing writing services for complete deliverables, we also offer flexible solutions for partnering with customers’ in-house writers to take on specific standalone document-related tasks, providing cost-effective solutions that remove the burden of routine medical writing tasks and allow our customers’ writers to focus on content development.All our solutions can be provided as part of full-service programs or as standalone solutions in a functional service partnership model.We draft wide range of documents for clinical trial submissions and other regulatory documents yoke with clinical research.The documents we cover are investigators’ brochures, study protocols, Informed consent, patient narratives, safety narratives, CSRs, selected e CTD modules, development safety update reports (DSURs), periodic safety update reports (PSURs) and annual safety reports (ASRs).