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5University CollegeISO 9001:2015 CertiedWorkshop onBioreactor Date : 14th November 2019 Organized byFaculty of Science Kelana Jaya Learning Site Lincoln University College, MalaysiaTel: +60378063478
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The Department of Biotechnology Leaflet CDR (Central Drug Registry) is a document that provides a structured format for the submission of data related to biotechnological products, ensuring compliance with regulatory standards.
Entities involved in the development, manufacturing, or distribution of biotechnological products are required to file the Department of Biotechnology Leaflet CDR.
To fill out the Department of Biotechnology Leaflet CDR, you need to provide accurate information as per the guidelines including product details, manufacturing processes, and safety data, ensuring all fields are completed as required.
The purpose of the Department of Biotechnology Leaflet CDR is to facilitate the regulatory review process for biotechnological products, ensuring they meet safety and efficacy standards before reaching the market.
The Department of Biotechnology Leaflet CDR must report details such as product description, active ingredients, mode of action, clinical trial data, manufacturing process, and safety information.
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