Clinical Trial
Management of the Data Safety Management Committee for Clinical Trials
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Clinical Trial
3 Hours Virtual Seminar: Latin America Understanding Regulatory Com...
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Clinical Trial
21 CFR Part 11 and Annex 11: What You Need to Know to Pass the New ...
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Clinical Trial
Electronic Records & Electronic Signatures; 21 Cfr Part 11; Basic C...
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Pharmaceutical
Transfer of Analytical Methods According to the USP Chapter <1224>
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Clinical Trial
Quality Management of Electronic Systems in Clinical Trial Investig...
Vidia Ramdeen
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Post-approval changes for medicinal products in the EU
Adriaan Fruijtier
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Conducting a Virtual GCP Audit of a CRO Managed Study during the CO...
Kelly Thomas
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Masters Certification program on Validation and Regulatory Acceptan...
Christopher R DeVany
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Mitigate Fiscal Risks in Clinical Trials: Coverage Analysis, Budget...
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Clinical Trial
The Impact of Final ICH GCP E6 R2 Guideline on Budgeting and Contra...
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Clinical Trial
Change Management Plan Development for Risk-Based Clinical Studies:...
Kelly Thomas
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Registration of Drugs Based on Monoclonal Antibodies (PRA05)
Kelly Thomas
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