Pharmaceutical Manufacturing Primer

- Level: Intermediate
- CPE: 1.0 Credits
- Time: 45 Minutes
Pharmaceutical Manufacturing Primer introduces the sequential stages involved in small molecule drug production, emphasizing the purpose and rationale behind each step. From chemical synthesis and purification to formulation and packaging, understand the manufacturing decisions and regulatory steps that impact cost, quality, and speed to market.
- Learn the steps of small molecule drug production and their effect on cost, timelines, and product quality
- Gain insight into quality control and quality assurance considerations to ensure regulatory compliance
- Learn key anti-counterfeiting strategies in pharmaceutical distribution to maximize ROI
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- Overview
- Agenda
- Features
- Justify This Training
- FAQ
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Agenda
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Chemical Synthesis
Outlines the types of reactions used to synthesize the active pharmaceutical ingredients (API).
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Purification
Explains the purpose of each API purification method and how supplier validation ensures the quality of manufacturing.
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Formulation
Lists the key formulation goals and the characteristics of the four most common pharmaceutical formulations.
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Packaging
Highlights key regulations and strategies in pharmaceutical packaging and chain supply.
Features
- Closed Captioning in English, Spanish, French, French Canadian, Hindi, Japanese, Korean, Mandarin, Russian, Standard Arabic
- Transcripts in English, Spanish, French, French Canadian, Hindi, Japanese, Korean, Mandarin, Russian, Standard Arabic
- Course materials
- Real-time tracking
- Progress reporting
- Accessibility features
- Corporate account upgrades
- LinkedIn certificate attachment
- Verified certificates
Justify This Training
View our “Justify This Training” checklist and letter to craft a persuasive request that clearly shows the value of Biotech Primer training to your role and your company. This step-by-step guide helps you highlight ROI, align with business goals, and increase your chances of getting this course approved.
FAQ
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