- Overview
- Agenda
- Features
- Justify This Training
- FAQ
Watch Trailer
Agenda
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Overview
Introduces key preclinical development metrics, including pharmacology and toxicology, to inform trial design and regulatory approval.
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Pharmacology
Explores core pharmacology concepts, including binding assays based on the Law of Mass Action, dose-response curves for potency and efficacy, and mechanisms of action for agonists and antagonists.
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Pharmacokinetics
Focuses on PD and PK measurements, including the ADME of drugs and bioanalytical assays to determine API concentration, informing dose, frequency, and route of administration.
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Toxicology
Describes the complexities of in vivo models, focusing on concordance between animal and human toxicities, and the importance of therapeutic margins and adverse effects.
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Nonclinical IND/CTA
Reviews the various types of INDs and the role of the Common Technical Document (CTD) in IND and CTA filings.
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
Our Executive
Certifications
Cannot make our live class? Consider one of our Executive Certifications.

Drug Development Executive Certification
- CPE:13.50 Credits
- Time:10.5 Hours
- Total:12 Courses

Drug Manufacturing Executive Certification
- CPE:14.50 Credits
- Time:10 Hours
- Total:11 Courses


