Ditemukan 6 dokumen yang sesuai dengan query
Faradina Astari Munandar, author
Praktik Kerja di Apotik Kimia Farma No. 267 Periode Bulan Februari tahun 2020/Praktik Kerja di Badan Pengawas Obat dan Makanan Periode Bulan Maret Tahun 2020/Praktik Kerja di PT. Mahakam Beta Farma Periode Bulan Juni - Juli Tahun 2020
Internship at Apotik Kimia Farma No. 267 Period February 2020/Internship at...
Depok: Fakultas Farmasi Universitas Indonesia, 2020
PR-pdf
UI - Tugas Akhir Universitas Indonesia Library
Gopalaswamy, Smita, author
Boca Raton: CRC Press, 2008
615.1 GOP c
Buku Teks Universitas Indonesia Library
Hanan Zhafirah, author
ABSTRAK
Industrialisasi dan ekspansi bisnis yang dijalankan dengan sistem pasar bebas di Amerika Serikat pada masa Progresif Era memberikan peluang kepada pebisnis produk makanan untuk melakukan tindak kecurangan. Ketiadaan regulasi dan standarisasi produk makanan membuat produsen makanan di Amerika Serikat leluasa untuk memproduksi dan menjual makanan yang tercemar. Skripsi ini menganalisis...
2017
S69686
UI - Skripsi (Membership) Universitas Indonesia Library
This book offers comprehensive, easy to understand guidance for medical device technology innovators on how to work through the United States FDA regulatory review process, while also providing insight on the various intellectual property concerns that many medical device innovators face. In the first portion of this book, readers are...
Switzerland: Springer Nature, 2019
e20508371
eBooks Universitas Indonesia Library
A step-by-step, integrated approach for successful, FDA-approved combination drug products Using a proven integrated approach to combination drug development, this book guides you step by step through all the preclinical, clinical, and manufacturing stages. Written from an FDA regulatory perspective, the book not only enables you to bring a successful...
Hoboken, New Jersey: John Wiley & Sons, 2008
e20385305
eBooks Universitas Indonesia Library
Weinberg, Sandy, author
This book guides the reader through FDA regulation guidelines and outlines a comprehensive strategy for cost reduction in regulatory affairs and compliance. This book explains six strategies to cost-effectively comply with FDA regulations while maintaining product safety and improving public access through cost controls. It provides useful and practical guidance...
Hoboken: John Wiley & Sons, 2011
e20377190
eBooks Universitas Indonesia Library