
2. Pharmaceutical Production (Non-Sterile & Sterile)

Quiz
•
Professional Development, Other, Specialty
•
University - Professional Development
•
Hard

Elpharma Multi Solution
Used 2+ times
FREE Resource
8 questions
Show all answers
1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Apa saja faktor yang termasuk dalam lahirnya produk di industri farmasi?
Permintaan Pasar
Epidemiologi
Toll Manufacturing
Semua benar
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Dalam proses pengembangan produk baru di industri farmasi, setelah R&D mengembangkan formulasi dan stabilitas skala lab, apa yang selanjutnya dilakukan?
Menyiapkan proses produksi skala komersil
Menyiapkan berkas untuk registrasi produk
Mengajukan proposal pilot & transfer teknologi pilot
Mengembangkan metode analisa
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Pada saat step produksi apakah analisa kelembaban tablet dilakukan?
Drying
Milling
Coating
Packing
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Produk yang dapat disterilisasi pada kemasan final produk disebut
Produk Sterilisasi Akhir
Produk Non-Steril
Produk Aseptis
Produk Antara
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Apabila formulasi produk dapat difiltrasi menggunakan filter microbial, maka proses sterilisasi yang dilakukan adalah?
Menggunakan autoklaf pada suhu 1210C selama 15 menit
Menggunakan kombinasi filtrasi aseptis dan proses aseptis
Menggunakan panas uap dengan Fo ≥ 8 menit
Menggunakan sinar UV
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Berikut ini adalah contoh produk injeksi volume besar, kecuali?
Larutan Elektrolit
Protein Nutrisi
Serbuk Liofilisasi
Emulsi lemak
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Apakah alat filling aseptis yang paling baik dan optimal dalam proteksi mikroba terhadap produk?
Isolator
Restricted Access Barrier Systems (RABS)
Laminar Air Flow (LAF)
Biosafety Cabinet
8.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Apakah Oritentasi Utama Apoteker dalam bagian Produksi?
Mengontrol bahan baku yang diterima (release/reject)
Membuat forecast produksi
Mengontrol pelulusan produk jadi
Merancang prosedur pembuatan sediaan steril/non-steril sesuai dengan ketentuan CPOB
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