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Yazar

Wiley InterScience (Online service)

(4)

Brody, Tom, author.

(2)

Kanfer, Isadore.

(2)

Shargel, Leon, 1941-

(2)

Adams, Michael, 1951-

(1)

Andrews, Paul A.

(1)

Berry, Ira R., 1942-

(1)

(1)

Carpenter, Daniel P., 1967- author.

(1)

Cayen, Mitchell N.

(1)

Chow, Shein-Chung, 1955-

(1)

Cohen, Jeffrey A. (Jeffrey Alan).

(1)

Davis, Kate (Kate G.)

(1)

Davis, Peter, ed.

(1)

Duke Clinical Research Institute.

(1)

(1)

(1)

Fulda, Thomas R.

(1)

Gad, Shayne C., 1948-

(1)

Gad, Shayne C., 1948- Safety pharmacology in pharmaceutical development and approval.

(1)

Gregersen, Jens-Peter.

(1)

Griffin, J. P. (John Parry)

(1)

Guarino, Richard A. ed.

(1)

Guarino, Richard A., 1935-

(1)

(1)

Hoberman, Alan M.

(1)

Holland, Leland Norman, 1957-

(1)

Hsiao, Chin-Fu, 1964-

(1)

Hynes, Martin D.

(1)

Kay, R. (Richard), 1949-

(1)

Khan, Firdos Alam. editor.

(1)

Lewis, Elise M.

(1)

Liu, Jen-pei, 1952-

(1)

Liu, Margaret B.

(1)

Liu, Margaret B. Lessons from a horse named Jim.

(1)

Martin, Robert P. (Robert Paul)

(1)

Nally, Joseph D.

(1)

Radomsky, Michael, editor.

(1)

Rudick, Richard A.

(1)

Senior, Judith, editor.

(1)

Siegel, Evan B.

(1)

SpringerLink (Online service)

(1)

Teicher, Beverly A., 1952-

(1)

Weinberg, Sandy, 1950-

(1)

Wertheimer, Albert I.

(1)

Tümünü genişlet

Dil

(30)

Yayın Yılı

-

(5)

(3)

(3)

(3)

(3)

(1)

(1)

(1)

(1)

(1)

(1)

(1)

(1)

(1)

(1)

(1)

(1)

(1)

Tümünü genişlet

Konu

(6)

United States. Food and Drug Administration.

(4)

Clinical Trials as Topic.

(3)

Drug Approval -- United States.

(3)

(3)

Drug approval -- United States.

(3)

Research Design.

(3)

Clinical Trials Data Monitoring Committees.

(2)

Clinical trials -- Design.

(2)

(2)

Drug Approval -- organization & administration.

(2)

(2)

Drug development.

(2)

Drugs -- Law and legislation -- United States.

(2)

Pharmaceutical policy -- United States.

(2)

(2)

(2)

Age Factors -- United States.

(1)

Antineoplastic Agents -- standards

(1)

Biological products -- United States.

(1)

Biotechnology -- Japan.

(1)

Biotechnology -- Patents.

(1)

Biotechnology -- Research.

(1)

Biotechnology -- United States.

(1)

Child -- United States.

(1)

Clinical Trials -- methods

(1)

Clinical Trials -- methods.

(1)

Clinical Trials as Topic

(1)

Clinical Trials as Topic -- ethics -- United States.

(1)

Clinical Trials as Topic -- legislation & jurisprudence -- United States.

(1)

Clinical Trials, Phase I as Topic.

(1)

Clinical trials -- Handbooks, manuals, etc.

(1)

Clinical trials -- Statistical methods.

(1)

Consumer Product Safety.

(1)

Device Approval -- United States.

(1)

Device Approval -- legislation & jurisprudence -- United States.

(1)

Drug Approval -- Japan.

(1)

Drug Approval -- economics.

(1)

Drug Approval -- legislation & jurisprudence.

(1)

Drug Approval -- legislation and jurisprudence -- United States.

(1)

Drug Approval -- methods.

(1)

Drug Combinations -- United States.

(1)

(1)

Drug Discovery -- methods.

(1)

Drug Evaluation -- methods.

(1)

Drug Evaluation, Preclinical

(1)

Drug Evaluation, Preclinical -- United States.

(1)

Drug Evaluation, Preclinical -- methods.

(1)

Drug Industry -- economics.

(1)

Drug Industry -- organization & administration -- Japan.

(1)

Drug Industry -- organization & administration -- United States.

(1)

Drug Therapy -- Handbooks

(1)

Drug Toxicity -- prevention & control -- United States.

(1)

Drug approval -- Safety regulations -- United States.

(1)

Drug approval -- Statistical methods.

(1)

Drugs -- Controlled release.

(1)

Drugs -- Research -- Standards -- United States.

(1)

Drugs -- Research -- United States.

(1)

Drugs -- Research.

(1)

Drugs -- Standards -- United States.

(1)

Drugs -- Testing -- Government policy -- United States.

(1)

Drugs -- Testing -- Handbooks, manuals, etc.

(1)

Drugs -- Testing -- Standards.

(1)

Drugs -- Testing -- Statistical methods.

(1)

Drugs -- Testing.

(1)

Drugs -- Toxicology -- United States.

(1)

(1)

Drugs, Investigational -- United States.

(1)

Drugs, Investigational -- therapeutic use.

(1)

Economics, Pharmaceutical -- legislation & jurisprudence.

(1)

Farmasötik Preparatlar -- El Kitapları

(1)

(1)

Government Agencies -- history.

(1)

Government Regulation.

(1)

Infant -- United States.

(1)

(1)

KAMU POLİTİKASI.

(1)

Klinik Çalışmalar -- yöntemler

(1)

Konu Başlıklarına Göre Klinik Çalışmalar

(1)

Magnetic Resonance Imaging

(1)

Manyetik Resonans Görüntüleme

(1)

Marketing -- methods.

(1)

Medical Informatics.

(1)

Medical instruments and apparatus -- United States.

(1)

Models, Animal -- United States.

(1)

Multiple Sclerosis -- pathology

(1)

Multiple Sclerosis -- therapy

(1)

Mültipl Skleroz -- patoloji

(1)

Mültipl Skleroz -- tedavi

(1)

New products -- Government policy -- United States.

(1)

Organizational Culture.

(1)

Outcome Assessment (Health Care)

(1)

Pediatric pharmacology -- Research -- United States.

(1)

Pharmaceutical Preparations -- Handbooks

(1)

Pharmaceutical Preparations -- economics.

(1)

Pharmaceutical biotechnology -- Law and legislation.

(1)

Pharmaceutical chemistry.

(1)

Pharmaceutical industry -- Data processing.

(1)

Pharmaceutical industry -- Quality control.

(1)

Pharmaceutical industry -- Statistical methods.

(1)

Pharmaceutical industry.

(1)

Pharmacology -- Data processing.

(1)

Pharmacology, Experimental.

(1)

Pharmacy -- Data processing.

(1)

Pharmacy -- Law and legislation -- United States.

(1)

Planning Techniques -- Japan.

(1)

Planning Techniques -- United States.

(1)

(1)

Research -- organization & administration -- Japan.

(1)

Research -- organization & administration -- United States.

(1)

(1)

(1)

(1)

Tablets (Medicine)

(1)

Technology, Pharmaceutical -- Japan.

(1)

Technology, Pharmaceutical -- United States.

(1)

Tümör Gidericiler -- standartlar

(1)

United States Food and Drug Administration.

(1)

(1)

United States. Food and Drug Administration

(1)

Vaccines -- Biotechnology.

(1)

Çıktı Değerlendirmesi (Sağlık Hizmeti)

(1)

İLAÇ ENDÜSTRİSİ.

(1)

İlaç Değerlendirme, Klinik Öncesi

(1)

İlaç Tasarımı

(1)

İlaç Tedavisi -- El Kitapları

(1)

İlaçlar, Jenerik

(1)

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1.

New drug approval process için kapak resmi

New drug approval process

New drug approval process

Yazar

Guarino, Richard A., 1935-

Yer Numarası

ONLINE

Elektronik Erişim

Distributed by publisher. Purchase or institutional license may be required for access.

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2.

New drug approval process için kapak resmi

New drug approval process

New drug approval process

Yazar

Guarino, Richard A. ed.

Yer Numarası

QV 704 DRU 1993 C.56 1.K

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3.

Anticancer drug development guide : preclinical screening, clinical trials, and approval için kapak resmi

Anticancer drug development guide : preclinical screening, clinical trials, and approval

Anticancer drug development guide : preclinical screening, clinical trials, and approval

Yazar

Teicher, Beverly A., 1952- Andrews, Paul A.

Yer Numarası

QV 269 A6295 2004

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4.

Nano Drug Delivery for Cancer Therapy Principles and Practices için kapak resmi

Nano Drug Delivery for Cancer Therapy Principles and Practices

Nano Drug Delivery for Cancer Therapy Principles and Practices

Yazar

Khan, Firdos Alam. editor. SpringerLink (Online service)

Yer Numarası

XX(522167.1)

Elektronik Erişim

https://doi.org/10.1007/978-981-99-6940-1

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5.

FDA's drug review process and the package label : strategies for writing successful FDA submissions için kapak resmi

FDA's drug review process and the package label : strategies for writing successful FDA submissions

FDA's drug review process and the package label : strategies for writing successful FDA submissions

Yazar

Brody, Tom, author.

Yer Numarası

ONLINE

Elektronik Erişim

ScienceDirect https://www.sciencedirect.com/science/book/9780128146477

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6.

Clinical trials : study design, endpoints and biomarkers, drug safety, and FDA and ICH guidelines için kapak resmi

Clinical trials : study design, endpoints and biomarkers, drug safety, and FDA and ICH guidelines

Clinical trials : study design, endpoints and biomarkers, drug safety, and FDA and ICH guidelines

Yazar

Brody, Tom, author.

Yer Numarası

ONLINE

Elektronik Erişim

ScienceDirect http://www.sciencedirect.com/science/book/9780128042175

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7.

Generic drug product development solid oral dosage forms için kapak resmi

Generic drug product development solid oral dosage forms

Generic drug product development solid oral dosage forms

Yazar

Shargel, Leon, 1941- Kanfer, Isadore.

Yer Numarası

ONLINE(342846.1)

Elektronik Erişim

Distributed by publisher. Purchase or institutional license may be required for access.

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8.

Design and analysis of bridging studies için kapak resmi

Design and analysis of bridging studies

Design and analysis of bridging studies

Yazar

Hsiao, Chin-Fu, 1964- Liu, Jen-pei, 1952- Chow, Shein-Chung, 1955-

Yer Numarası

ONLINE

Elektronik Erişim

Distributed by publisher. Purchase or institutional license may be required for access.

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9.

Pediatric nonclinical drug testing principles, requirements, and practices için kapak resmi

Pediatric nonclinical drug testing principles, requirements, and practices

Pediatric nonclinical drug testing principles, requirements, and practices

Yazar

Hoberman, Alan M. Lewis, Elise M.

Yer Numarası

ONLINE

Elektronik Erişim

Connect to MyiLibrary resource
Wiley InterScience An electronic book accessible through the World Wide Web; click for information

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10.

Safety pharmacology in pharmaceutical development approval and post marketing surveillance için kapak resmi

Safety pharmacology in pharmaceutical development approval and post marketing surveillance

Safety pharmacology in pharmaceutical development approval and post marketing surveillance

Yazar

Gad, Shayne C., 1948- Gad, Shayne C., 1948- Safety pharmacology in pharmaceutical development and approval.

Yer Numarası

ONLINE

Elektronik Erişim

Distributed by publisher. Purchase or institutional license may be required for access.

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11.

Clinical trials study design, endpoints and biomarkers, drug safety, and FDA and ICH guidelines için kapak resmi

Clinical trials study design, endpoints and biomarkers, drug safety, and FDA and ICH guidelines

Clinical trials study design, endpoints and biomarkers, drug safety, and FDA and ICH guidelines

Yazar

Brody, Tom.

Yer Numarası

ONLINE

Elektronik Erişim

ScienceDirect An electronic book accessible through the World Wide Web; click for information

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12.

Pharmaceutical lifecycle management making the most of each and every brand

Pharmaceutical lifecycle management making the most of each and every brand

Yazar

Ellery, Tony. Hansen, Neal. Wiley InterScience (Online service)

Yer Numarası

ONLINE

Elektronik Erişim

Wiley InterScience An electronic book accessible through the World Wide Web; click for information

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Çevrimiçi Kütüphane~1

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