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Description
"This eLearning course from USP provides a basic understanding of the challenges and goals confronting a regulatory professional when defining a global regulatory strategy. It provides an overview of the regulatory considerations in the major regions of the world where marketing applications are pursued and compares the application requirements in these regions. It also includes a description of the regulatory tools"" at the disposal of the regulatory professional and discusses reimbursement considerations and how they may affect both a global development and regulatory strategy. Finally, the course provides insight into the roles of cross-functional strategy teams. Collectively, this knowledge is critical to creating a global regulatory strategy for pharmaceuticals introduced in global markets."
Miscellaneous
Certificate of Analysis (specimen)
Reference Material CoA specimen: for the current lot, please contact your customer service representative at info@labmix24.com
Product data sheet
View all available product details e.g. description, analytes/parameters, CAS Number, concentrations/values, sales unit/product format, method, source, transport information
US Pharmacopeia Standards set a global benchmark, enabling efficient, reliable, and cost-effective development and quality control of pharmaceuticals.
Official USP Reference Standards are highly characterized physical specimens intended for quality control use when conducting assays and tests for medicines as described in the USP-NF. When you conduct tests and assays required by the USP-NF using the USP reference standards specified, the results can be considered conclusive.
As a USP-Authorized Distributor, we offer the following products and services:
- USP Reference Standards
- USP Pharmaceutical Analytical Impurities
- USP Training and educational programs