Search Results for Drugs -- Standards.

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Yazar

Berry, Ira R., 1942-

(2)

(1)

Bohaychuk, Wendy.

(1)

Cartwright, A. C. (Anthony C.), 1940-

(1)

(1)

Clontz, Lucia. Microbial limit and bioburden tests for the pharmaceutical industry.

(1)

Cloud, Phillip A.

(1)

Coelho, Paulo G. editor.

(1)

Gopalaswamy, Smita.

(1)

Gopalaswamy, Venky.

(1)

Guarino, Richard A., 1935-

(1)

Harpaz, Daniel.

(1)

Hynes, Martin D.

(1)

Light, Donald, Jr., 1942-

(1)

Matthews, Brian (Brian R.)

(1)

Medina, Carmen.

(1)

Melville, James C. editor. (orcid)

(1)

(1)

Mills, Terry. Instrumental data for drug analysis.

(1)

Nally, Joseph D.

(1)

Nash, Robert A., 1930-

(1)

(1)

Rosenbaum, Deborah.

(1)

Sahajwalla, Chandrahas G.

(1)

Segalstad, Siri.

(1)

Sharp, John, 1930-

(1)

Smith, Fred, M.D.

(1)

SpringerLink (Online service)

(1)

Wiley InterScience (Online service)

(1)

Willig, Sidney H., 1919-

(1)

World Health Organization.

(1)

Young, Simon. editor. (orcid)

(1)

Tümünü genişlet

Dil

(21)

Yayın Yılı

-

(3)

(2)

(2)

(2)

(2)

(2)

(2)

(1)

(1)

(1)

(1)

(1)

(1)

(1)

Tümünü genişlet

Konu

Drugs -- Standards -- United States.

(7)

Pharmaceutical industry -- Quality control.

(6)

Drugs -- Testing -- Standards.

(5)

United States. Food and Drug Administration.

(4)

Drugs -- Standards.

(3)

Drug Industry -- standards.

(2)

Pharmaceutical industry -- Standards.

(2)

Pharmaceutical technology -- Standards.

(2)

Biological products -- Standards -- United States.

(1)

Clinical trials -- Law and legislation -- United States.

(1)

Clinical trials -- Standards.

(1)

Clinical trials.

(1)

Controle de qualidade

(1)

Drug Evaluation -- standards.

(1)

Drug Evaluation, Preclinical.

(1)

Drug Industry -- standards -- Europe.

(1)

Drug Industry -- standards -- United States.

(1)

(1)

Drug and Narcotic Control.

(1)

Drug approval -- United States.

(1)

Drug development.

(1)

Drugs -- Analysis -- Laboratory manuals.

(1)

Drugs -- Analysis -- Standards.

(1)

Drugs -- Law and legislation -- European Union Countries.

(1)

Drugs -- Law and legislation -- United States.

(1)

Drugs -- Law and legislation.

(1)

Drugs -- Microbiology -- Standards.

(1)

Drugs -- Quality control.

(1)

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

(1)

Drugs -- Risk factors.

(1)

Drugs -- Spectra -- Standards.

(1)

Drugs -- Standards -- European Union Countries.

(1)

Drugs -- Standards -- Laboratory manuals.

(1)

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

(1)

Drugs -- Testing -- Law and legislation -- United States.

(1)

Drugs -- standards.

(1)

Guideline Adherence -- Europe.

(1)

Guideline Adherence -- United States.

(1)

Informatics -- standards -- Europe.

(1)

Informatics -- standards -- United States.

(1)

Instrumental analysis -- Standards.

(1)

Legislation, Drug.

(1)

Medical instruments and apparatus -- Standards -- United States.

(1)

Medical instruments and apparatus -- Standards.

(1)

Medicamentos (analise e avaliacao)

(1)

Medicamentos (vigilancia sanitaria)

(1)

Medication Errors -- prevention & control.

(1)

Microbial contamination -- Measurement -- Standards.

(1)

New products -- Government policy -- United States.

(1)

Pharmaceutical chemistry.

(1)

Pharmaceutical industry -- European Union Countries -- Quality control.

(1)

Pharmaceutical industry -- Risk management.

(1)

Pharmaceutical industry -- United States -- Quality control.

(1)

Pharmaceutical policy -- United States.

(1)

Prescription Drugs -- standards.

(1)

Quality Control -- Europe.

(1)

Quality Control -- United States.

(1)

Quality Control.

(1)

Risk Assessment.

(1)

Technology -- standards -- Europe.

(1)

Technology -- standards -- United States.

(1)

(1)

İLAÇLAR -- STANDARTLAR.

(1)

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13.

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.

Yer Numarası

ONLINE

Elektronik Erişim

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

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14.

New drug development regulatory paradigms for clinical pharmacology and biopharmaceutics için kapak resmi

New drug development regulatory paradigms for clinical pharmacology and biopharmaceutics

New drug development regulatory paradigms for clinical pharmacology and biopharmaceutics

Yazar

Sahajwalla, Chandrahas G.

Yer Numarası

ONLINE

Elektronik Erişim

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15.

Pharmaceutical process validation için kapak resmi

Pharmaceutical process validation

Pharmaceutical process validation

Yazar

Berry, Ira R., 1942- Nash, Robert A., 1930-

Yer Numarası

ONLINE

Elektronik Erişim

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16.

Physician investigator handbook GCP tools and techniques için kapak resmi

Physician investigator handbook GCP tools and techniques

Physician investigator handbook GCP tools and techniques

Yazar

Rosenbaum, Deborah. Smith, Fred, M.D.

Yer Numarası

ONLINE

Elektronik Erişim

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17.

Validation of active pharmaceutical ingredients için kapak resmi

Validation of active pharmaceutical ingredients

Validation of active pharmaceutical ingredients

Yazar

Berry, Ira R., 1942- Harpaz, Daniel.

Yer Numarası

ONLINE

Elektronik Erişim

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18.

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., 1919-

Yer Numarası

ONLINE

Elektronik Erişim

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19.

Conducting GCP-compliant clinical research için kapak resmi

Conducting GCP-compliant clinical research

Conducting GCP-compliant clinical research

Yazar

Bohaychuk, Wendy. Ball, Graham.

Yer Numarası

ONLINE

Elektronik Erişim

John Wiley http://dx.doi.org/10.1002/0470846267

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20.

How to develop and manage qualification protocols for FDA compliance için kapak resmi

How to develop and manage qualification protocols for FDA compliance

How to develop and manage qualification protocols for FDA compliance

Yazar

Cloud, Phillip A.

Yer Numarası

ONLINE

Elektronik Erişim

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21.

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

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22.

How to develop and implement a national drug policy. için kapak resmi

How to develop and implement a national drug policy.

How to develop and implement a national drug policy.

Yer Numarası

QV 704 H847 1988

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