Sunday 10 June 2018

Pharmaceutical Analysis determines the quality of drug products via analytical chemistry.  This course will introduce areas such as method validation, handling raw materials and finished products, documentations, inspections that impact the development of pharmaceutical products. Throughout this course, critical cGMPs regulations, FDA guidances and ICH Quality guidelines will be discussed specifically emphasizing procedures to help individuals to maintain a high level of compliance that rounds the laboratory environment.  It also reviews several quality systems that support the analytical.

Click the link for more info:https://asiapacific.pharmaceuticalconferences.com/

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