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World Health Organization.

(4)

Haider, Syed Imtiaz.

(2)

SpringerLink (Online service)

(2)

Wiley InterScience (Online service)

(2)

Al-Worafi, Yaser Mohammed. editor.

(1)

Berry, Ira R., ed.

(1)

Bhattacharyya, Lokesh.

(1)

Bliesner, David M.

(1)

Chen, Ding-Geng.

(1)

(1)

Davis, Charles B. (Charles Baldwin)

(1)

(1)

Hill, Suzanne. editor.

(1)

Huber, Ludwig, 1948-

(1)

International pharmaceutical technology symposium (19th : 2018 : Antalya,Turkey)

(1)

John Wiley & Sons.

(1)

Koren, Gideon. editor.

(1)

Light, Donald, Jr., 1942-

(1)

MacLeod, Stuart. editor.

(1)

McCormick, Kate.

(1)

Medina, Carmen, ed.

(1)

Nash, Robert A., ed.

(1)

Peace, Karl E., 1941-

(1)

Qiu, Fenghe, editor.

(1)

Rane, Anders. editor.

(1)

Rodriguez, Jackelyn, author.

(1)

Rohrer, Jeffrey S.

(1)

Sarker, Dipak K.

(1)

Scrivens, Garry, editor.

(1)

Segalstad, Siri.

(1)

WHO Expert Committee on Specifications for Pharmaceutical Preparations.

(1)

Wang, Binghe, PhD.

(1)

Willig, Sidney H.

(1)

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Tümünü genişlet

Konu

Drug Industry -- standards.

(9)

Drug Industry -- standards -- United States.

(4)

Pharmaceutical industry -- Quality control.

(4)

Drug Industry -- standards

(3)

Quality Control -- United States.

(3)

Quality Control.

(3)

Drug Industry -- standards -- Congresses

(2)

Drugs -- Standards.

(2)

Nitelik Denetimi

(2)

Pharmaceutical Preparations -- standards -- United States.

(2)

Pharmaceutical industry -- Standards.

(2)

Quality Control

(2)

İLAÇ ENDÜSTRİSİ -- STANDARTLAR.

(2)

İlaç Endüstrisi -- satandartlar -- Kongreler

(2)

İlaç Endüstrisi -- standartlar

(2)

(1)

Araç-Gereç Güvenliği -- standartlar

(1)

Araç-Gereç ve Donamımlar -- standartlar

(1)

Biological Agents -- analysis.

(1)

Biological Products -- standards -- United States.

(1)

Biological products -- Analysis.

(1)

Biotechnology -- standards

(1)

Biyoteknoloji -- standartlar

(1)

BİYOLOJİK ÜRÜNLER -- STANARTLAR -- A.B.D.

(1)

Chemistry, Analytical -- standards

(1)

Chemistry, Pharmaceutical -- standards

(1)

Chromatography, Ion Exchange -- methods.

(1)

Clinical trials.

(1)

Controle de qualidade

(1)

DONATI VE SAĞLANTILAR -- STANDARTLAR -- A.B.D.

(1)

Drug Discovery.

(1)

Drug Evaluation -- standards -- United States

(1)

Drug Evaluation, Preclinical.

(1)

Drug Industry -- legislation & jurisprudence -- United States.

(1)

Drug Industry -- standards -- Europe.

(1)

Drug Industry -- standards -- Handbooks.

(1)

Drug Industry -- standards -- United States

(1)

Drug Stability.

(1)

(1)

Drug and Narcotic Control.

(1)

Drug development.

(1)

Drug industry -- Standards.

(1)

Drug stability -- Statistical methods.

(1)

Drugs -- Metabolism.

(1)

Drugs -- Quality control.

(1)

Drugs -- Risk factors.

(1)

Drugs -- Testing.

(1)

Equipment Safety -- standards

(1)

Equipment and Supplies -- standards

(1)

Equipment and Supplies -- standards -- United States.

(1)

FARMASÖTİK PREPARATLAR -- STANDARTLAR -- A:B.D.

(1)

FARMASÖTİK PREPARATLAR -- STANDARTLAR -- ABD.

(1)

Farmasötik Preparatlar -- Standartlar.

(1)

Farmasötik Preparatlar -- satandartlar -- Kongreler

(1)

Guideline Adherence -- Europe.

(1)

Guideline Adherence -- United States.

(1)

Informatics -- standards -- Europe.

(1)

Informatics -- standards -- United States.

(1)

Ion exchange chromatography.

(1)

KALİTE KONTROL -- A.B.D.

(1)

KALİTE KONTROL -- ABD.

(1)

Kimya, Analitik -- standartlar

(1)

Kimya, Farmasötik -- standartlar

(1)

Laboratories -- legislation & jurisprudence -- United States.

(1)

Laboratories -- standards

(1)

Laboratories -- standards -- United States.

(1)

Laboratuvarlar -- standartlar

(1)

Legislation, Drug -- United States.

(1)

Legislation, Drug.

(1)

Management Audit -- methods -- United States.

(1)

Mass Spectrometry.

(1)

Medicamentos (analise e avaliacao)

(1)

Medicamentos (vigilancia sanitaria)

(1)

Medication Errors -- prevention & control.

(1)

Nitelik Denetimi -- ABD

(1)

Pharmaceutical Preparations -- analysis.

(1)

Pharmaceutical Preparations -- metabolism.

(1)

Pharmaceutical Preparations -- standards -- Congresses

(1)

Pharmaceutical Preparations -- standards -- Handbooks.

(1)

Pharmaceutical industry -- Law and legislation -- United States.

(1)

Pharmaceutical industry -- Risk management.

(1)

Pharmaceutical industry.

(1)

Pharmaceutical policy -- United States.

(1)

Pharmaceutical preparations -- standards.

(1)

Pharmaceutical technology -- Standards.

(1)

Pharmaceutical technology.

(1)

Pharmacokinetics.

(1)

Pharmacology -- methods.

(1)

Prediction theory.

(1)

Prescription Drugs -- standards.

(1)

Quality Control -- Europe.

(1)

Quality Control -- Handbooks.

(1)

Quality Control -- United States

(1)

Risk Assessment.

(1)

TEKNOLOJİ, FARMASÖTİK -- STANDARTLAR

(1)

TEKNOLOJİ,FARMASÖTİK -- STANDARTLAR -- ABD.

(1)

Technology -- standards -- Europe.

(1)

Technology -- standards -- United States.

(1)

Technology, Pharmaceutical

(1)

Technology, Pharmaceutical -- standards

(1)

Technology, Pharmaceutical -- standards -- Handbooks.

(1)

Technology, Pharmaceutical -- standards -- United States.

(1)

Teknoloji, Farmasötik

(1)

(1)

United States. Food and Drug Administration.

(1)

YASALAR, İLAÇ -- ABD.

(1)

İLAÇ ENDÜSTRİSİ -- STANDARTLAR

(1)

İLAÇ ENDÜSTRİSİ -- STANDARTLAR -- A.B.D.

(1)

İLAÇ ENDÜSTRİSİ -- STANDARTLAR -- ABD.

(1)

İlaç Değerlendirme -- standartlar -- ABD

(1)

İlaç Endüstrisi -- Standartlar.

(1)

İlaç Endüstrisi -- standartlar -- ABD

(1)

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13.

WHO Expert Committee on Specifications for Pharmaceutical Preparations : fortieth report. için kapak resmi

WHO Expert Committee on Specifications for Pharmaceutical Preparations : fortieth report.

WHO Expert Committee on Specifications for Pharmaceutical Preparations : fortieth report.

Yazar

WHO Expert Committee on Specifications for Pharmaceutical Preparations. World Health Organization.

Yer Numarası

QV 771 W628 2006

Format:

Durum

Sağlık Bilimleri Kütüphanesi~1

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14.

Establishing a CGMP laboratory audit system a practical guide için kapak resmi

Establishing a CGMP laboratory audit system a practical guide

Establishing a CGMP laboratory audit system a practical guide

Yazar

Bliesner, David M. John Wiley & Sons.

Yer Numarası

ONLINE

Elektronik Erişim

John Wiley http://dx.doi.org/10.1002/0471784788

Format:

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15.

Validation standard operating procedures : a step-by-step guide for achieving compliance in the pharmaceutical, medical device, and biotech industries için kapak resmi

Validation standard operating procedures : a step-by-step guide for achieving compliance in the pharmaceutical, medical device, and biotech industries

Validation standard operating procedures : a step-by-step guide for achieving compliance in the pharmaceutical, medical device, and biotech industries

Yazar

Haider, Syed Imtiaz.

Yer Numarası

W 26 H149 2006

Format:

Durum

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16.

Quality assurance of pharmaceuticals : A Compendium of guidelines and related materials için kapak resmi

Quality assurance of pharmaceuticals : A Compendium of guidelines and related materials

Quality assurance of pharmaceuticals : A Compendium of guidelines and related materials

Yazar

World Health Organization.

Yer Numarası

QV 33 Q1 2004

Format:

Durum

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17.

Compliance handbook for pharmaceuticals, medical devices, and biologics için kapak resmi

Compliance handbook for pharmaceuticals, medical devices, and biologics

Compliance handbook for pharmaceuticals, medical devices, and biologics

Yazar

Medina, Carmen, ed.

Yer Numarası

QV 736 C7375 2004

Format:

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18.

Pharmaceutical process validation için kapak resmi

Pharmaceutical process validation

Pharmaceutical process validation

Yazar

Berry, Ira R., ed. Nash, Robert A., ed.

Yer Numarası

QV 771 P536 2003 V.129

Format:

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19.

Quality için kapak resmi

Yazar

McCormick, Kate.

Yer Numarası

ONLINE

Elektronik Erişim

ScienceDirect http://www.sciencedirect.com/science/book/9780750651134

Format:

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20.

Pharmaceutical master validation plan : the ultimate guide to FDA, GMP, and GLP compliance için kapak resmi

Pharmaceutical master validation plan : the ultimate guide to FDA, GMP, and GLP compliance

Pharmaceutical master validation plan : the ultimate guide to FDA, GMP, and GLP compliance

Yazar

Haider, Syed Imtiaz.

Yer Numarası

QV 736 H149 2002

Format:

Durum

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21.

Good manufacturing practices for pharmaceuticals : a plan for total quality control from manufacturer to consumer için kapak resmi

Good manufacturing practices for pharmaceuticals : a plan for total quality control from manufacturer to consumer

Good manufacturing practices for pharmaceuticals : a plan for total quality control from manufacturer to consumer

Yazar

Willig, Sidney H.

Yer Numarası

QV 771 W732 2001

Format:

Durum

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22.

Quality assurance of pharmaceuticals : a compendium of guidelines and related materials. için kapak resmi

Quality assurance of pharmaceuticals : a compendium of guidelines and related materials.

Quality assurance of pharmaceuticals : a compendium of guidelines and related materials.

Yazar

World Health Organization.

Yer Numarası

QV 33 Q1 1999 C.2

Format:

Durum

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23.

Microbial limit and bioburden tests for the pharmaceutical industry : validation approaches and global requirements için kapak resmi

Microbial limit and bioburden tests for the pharmaceutical industry : validation approaches and global requirements

Microbial limit and bioburden tests for the pharmaceutical industry : validation approaches and global requirements

Yazar

Clontz, Lucia.

Yer Numarası

QV 771 C644 1998

Format:

Durum

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24.

Quality assurance of pharmaceuticals : A Compendium of guidelines and related materials. için kapak resmi

Quality assurance of pharmaceuticals : A Compendium of guidelines and related materials.

Quality assurance of pharmaceuticals : A Compendium of guidelines and related materials.

Yazar

World Health Organization.

Yer Numarası

QV 736 Q11 1997 C.1

Format:

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