{"product_id":"9781118302064","title":"Pharmacovigilance Medical Writing: A Good Practice Guide","description":"\u003ci\u003ePharmacovigilance Medical Writing\u003c\/i\u003e covers the preparation of pharmacovigilance documents for all stages of the drug development process (i.e. from clinical development through to applications for marketing authorisations to the post-marketing stage). For each document, the book presents a review of the regulatory framework that governs the content of the document, followed by practical guidance (e.g. scheduling, source data, department\/functions involved in document preparation\/review, appropriate timelines and planning activities), ending with a generic model document compliant with the current guidelines, which can be modified to meet specific company and product requirements.","brand":"Wiley","offers":[{"title":"Default Title","offer_id":47121483825392,"sku":"9781118302064","price":49.99,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0737\/7593\/9824\/files\/9781118302064_p0.jpg?v=1769888088","url":"https:\/\/shop-qa.barnesandnoble.com\/products\/9781118302064","provider":"Barnes \u0026 Noble (DEV)","version":"1.0","type":"link"}