Isbn: 9786207823321 - the high tech manufacturer: good manufacturing practices for active substances used as raw materials in pharmaceuticals (8 résultats)

Etat : New.

Taschenbuch. Etat : Neu. The High Tech Manufacturer | Good Manufacturing Practices for Active Substances Used as Raw Materials in Pharmaceuticals | Abdoul Hamid Derra | Taschenbuch | Englisch | 2025 | Our Knowledge Publishing | EAN 9786207823321 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu.…

Etat : New.

Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware 216 pp. Englisch.

Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - These good practices come from part II of the European guide to good manufacturing practices for medicinal products for human and veterinary use, itself taken from the ICH Q7A guide developed by the international harmonization conference (ICH). These good practices are intended to provide a guide to good manufacturing practices (GMP) for the manufacture of active substances under an appropriate quality management system. They are also intended to provide assistance in ensuring that active substances comply with the quality and purity requirements they claim or are expected to have. In these good practices, 'Manufacturing' includes all operations of reception of materials, production, packaging, repackaging, labeling, relabeling, quality control, release, destocking and distribution of active substances as well as any associated controls. The term 'Must' indicates the recommendations that are expected to be followed, unless it can be demonstrated that they are not applicable, are supplemented by specific GMP guidelines, or are superseded by other measures.…

Taschenbuch. Etat : Neu. This item is printed on demand - Print on Demand Titel. Neuware -These good practices come from part II of the European guide to good manufacturing practices for medicinal products for human and veterinary use, itself taken from the ICH Q7A guide developed by the international harmonization conference (ICH). These good practices are intended to provide a guide to good manufacturing practices (GMP) for the manufacture of active substances under an appropriate quality management system. They are also intended to provide assistance in ensuring that active substances comply with the quality and purity requirements they claim or are expected to have. In these good practices, 'Manufacturing' includes all operations of reception of materials, production, packaging, repackaging, labeling, relabeling, quality control, release, destocking and distribution of active substances as well as any associated controls. The term 'Must' indicates the recommendations that are expected to be followed, unless it can be demonstrated that they are not applicable, are supplemented by specific GMP guidelines, or are superseded by other measures.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 216 pp. Englisch.…

Etat : New. Print on Demand.

Etat : New. PRINT ON DEMAND.