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macrocare offers a wide range of high-quality write services for companies biotech, pharmaceutical and medical devices around the world. Our team of qualified and experienced medical writers is well prepared to write a wide range of regulatory, clinical, scientific and marketing communication documents.
macrocare has a comprehensive understanding of different regulatory guidelines such as I-GCP, FDA, EMA guidelines. Our team consists of people with qualifications in medical, pharmaceutical and other life science themes (MBBS, MD, PhD and Masters) has know-how about therapeutic areas.
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With years of practical experience, our medical writers have the know-how to understand complex medical information and data and to prepare complex documents and publications in accordance with the relevant guidelines. If you help you in this process, qualified theme experts (SMEs), biostatistics, data analysts, quality analysts and the machining and language support team. Our medical wrote team in the US Reviews documents intended for US applications.All documents are managed, created, created, called, shared, changed and stored in a validated web-based document management system.
macrocare also offers medical write services on Japanese, French and German languages.
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