最高のASQ CPGP関連日本語版問題集 & 合格スムーズCPGP学習関連題 | 認定するCPGP参考資料これらの有用な知識をよりよく吸収するために、多くの顧客は、実践する価値のある種類のCPGP練習資料を持ちたいと考えています。 すべてのコンテンツは明確で、CPGP実践資料で簡単に理解できます。 リーズナブルな価格とオプションのさまざまなバージョンでアクセスできます。 すべてのコンテンツは、CPGP試験の規制に準拠しています。 あなたが成功すると決心している限り、CPGP学習ガイドはあなたの最善の信頼になります。 ASQ Certified Pharmaceutical GMP Professional 認定 CPGP 試験問題 (Q66-Q71):質問 # 66
In the context of sampling processes, why is it necessary to ensure sampling utensils are appropriately cleaned or are single-use?
Response:
A. To prevent cross-contamination and ensure accurate sampling results
B. To make the cleaning process more challenging
C. To increase the aesthetic appeal of the sampling process
D. To comply with employee preferences
正解：A
質問 # 67
The primary goal of compressed air and gas system regulations in pharmaceutical manufacturing is to:
Response:
A. Ensure the purity and safety of compressed air and gases used in production
B. Make the systems a focal point during facility tours
C. Allow for the personalization of air and gas systems by employees
D. Enhance the overall look of the manufacturing area
正解：A
質問 # 68
The use of PAT tools in manufacturing supports:
Response:
A. Reduced understanding of processes
B. Decreased product quality
C. Increased downtime
D. The manufacture of quality products
正解：D
質問 # 69
What is a key method to minimize the risk of material mix-ups?
Response:
A. Implementing lot-control methods and proper labeling
B. Using the same storage containers for all materials
C. Storing all materials together to save space
D. Assigning storage based on the material's color
正解：A
質問 # 70
What are the goals of a metrology program in pharmaceutical manufacturing?
(Choose two)
Response:
A. Showcasing the facility's technological advancements on social media
B. Achieving celebrity endorsements for the manufacturing process
C. Maintaining compliance with regulatory requirements