Expertise That Spans the Globe

Teva has the full range of Development expertise:

	Pharmacology, Toxicology, Pharmacokinetics & ADME.
	The Chemistry Manufacturing & Control and Biological development manufactures the drug substance and drug product.
	Phase I/Clinical Pharmacology, Pharmacokinetics, Biostatistics, Data Management and Programming, Medical Monitoring and Clinical QC.
	Regulatory CMC, Medical Assessment and Writing.
	Overall GxP compliance including GMP, GCP and GLP.

In addition, our global presence provides us with unique insight into both the major and emerging markets, knowledge we then incorporate into our development plan for emerging therapeutic fields. Use the interactive map below to view Teva's Development facilities across the globe. You can also view Teva's Manufacturing and/or Marketing facilities by selecting the appropriate tab within the map.