Pharmaceutical manufacturing handbook [Elektronisk resurs] regulations and quality / [edited by] Shayne Cox Gad.

• PHARMACEUTICAL MANUFACTURING HANDBOOK Regulations and Quality; CONTRIBUTORS; CONTENTS; PREFACE; SECTION 1 GOOD MANUFACTURING PRACTICES (GMP) AND OTHER FDA GUIDELINES; SECTION 2 INTERNATIONAL REGULATIONS OF GOOD MANUFACTURING PRACTICES; SECTION 3 QUALITY; SECTION 4 PROCESS ANALYTICAL TECHNOLOGY (PAT); SECTION 5 PERSONNEL; SECTION 6 CONTAMINATION AND CONTAMINATION CONTROL; SECTION 7 DRUG STABILITY; SECTION 8 VALIDATION; INDEX.

• Everything you need to ensure full compliance and superior quality control. With its coverage of Food and Drug Administration regulations, international regulations, good manufacturing practices, and process analytical technology, this handbook. 

Ämnesord

Pharmaceutical technology  -- Quality control -- Handbooks, manuals, etc. (LCSH)

Pharmaceutical industry  -- Law and legislation -- United States -- Handbooks, manuals, etc. (LCSH)

Drug Industry  -- legislation & jurisprudence -- United States. (MeSH)

Drug Evaluation  -- legislation & jurisprudence -- United States. (MeSH)

Quality Control  -- United States. (MeSH)

Techniques pharmaceutiques  -- Qualité -- Contrôle -- Guides, manuels, etc. (Vedettes-matière)

Industrie pharmaceutique  -- Droit -- États-Unis -- Guides, manuels, etc. (Vedettes-matière)

MEDICAL  -- Drug Guides. (bisacsh)

MEDICAL  -- Pharmacology. (bisacsh)

MEDICAL  -- Pharmacy. (bisacsh)

MEDICAL  -- Nursing -- Pharmacology. (bisacsh)

Drug Evaluation. 

Drug Industry. 

Pharmaceutical industry. 

Pharmaceutical technology. 

Quality control. 

Genre

Electronic books. 

Klassifikation

RS192 (LCC)

QV 33 AA1 (NLM)

MED (ämneskategori)

MED (ämneskategori)

MED (ämneskategori)

MED (ämneskategori)

615/.19 (DDC)

Pmca (kssb/8 (machine generated))