Using Medicare administrative data to conduct postmarketing surveillance of follow-on biologics: issues and opportunities.
Publication
, Journal Article
DiMartino, LD; Curtis, LH; Williams, RL; Abernethy, DR; Schulman, KA
Published in: Food Drug Law J
2008
Duke Scholars
Published In
Food Drug Law J
ISSN
1064-590X
Publication Date
2008
Volume
63
Issue
4
Start / End Page
891 / 900
Location
United States
Related Subject Headings
- United States
- Therapeutic Equivalency
- Product Surveillance, Postmarketing
- Medicare
- Law
- Investigational New Drug Application
- International Classification of Diseases
- Insurance Claim Reporting
- Humans
- Healthcare Common Procedure Coding System
Citation
APA
Chicago
ICMJE
MLA
NLM
DiMartino, L. D., Curtis, L. H., Williams, R. L., Abernethy, D. R., & Schulman, K. A. (2008). Using Medicare administrative data to conduct postmarketing surveillance of follow-on biologics: issues and opportunities. Food Drug Law J, 63(4), 891–900.
DiMartino, Lisa D., Lesley H. Curtis, Roger L. Williams, Darrell R. Abernethy, and Kevin A. Schulman. “Using Medicare administrative data to conduct postmarketing surveillance of follow-on biologics: issues and opportunities.” Food Drug Law J 63, no. 4 (2008): 891–900.
DiMartino LD, Curtis LH, Williams RL, Abernethy DR, Schulman KA. Using Medicare administrative data to conduct postmarketing surveillance of follow-on biologics: issues and opportunities. Food Drug Law J. 2008;63(4):891–900.
DiMartino, Lisa D., et al. “Using Medicare administrative data to conduct postmarketing surveillance of follow-on biologics: issues and opportunities.” Food Drug Law J, vol. 63, no. 4, 2008, pp. 891–900.
DiMartino LD, Curtis LH, Williams RL, Abernethy DR, Schulman KA. Using Medicare administrative data to conduct postmarketing surveillance of follow-on biologics: issues and opportunities. Food Drug Law J. 2008;63(4):891–900.
Published In
Food Drug Law J
ISSN
1064-590X
Publication Date
2008
Volume
63
Issue
4
Start / End Page
891 / 900
Location
United States
Related Subject Headings
- United States
- Therapeutic Equivalency
- Product Surveillance, Postmarketing
- Medicare
- Law
- Investigational New Drug Application
- International Classification of Diseases
- Insurance Claim Reporting
- Humans
- Healthcare Common Procedure Coding System