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Titles
- E11(R1) addendum: clinical investigation of medicinal products in the pediatric population1
- E17 general principles for planning and design of multiregional clinical trials1
- E18 genomic sampling and management of genomic data1
- E6(R2) good clinical practice: integrated addendum to ICH E6(R1)1
- Electronic health record adoption and interoperability among U.S. skilled nursing facilities and home health agencies in 20171
- Elemental impurities in drug products1
- Enforcement policy--OTC sunscreen drug products marketed without an approved application1
- Entities generally met Federal Select Agent Program internal inspection requirements, but CDC could do more to improve effectiveness1
- Entities' experiences and perceptions of reporting the theft, loss, or release of select agents or toxins to CDC1
- Establishing effectiveness for drugs intended to treat male hypogonadotropic hypogonadism attributed to nonstructural disorders1
- Explaining Stewart v. Azar: implications of the court's decision on Kentucky's Medicaid waiver1
- Extension of certain tobacco product compliance deadlines related to the final deeming rule: (revised)1