Booklets

Carry your GMP's with you All our booklets fits in your pocket and have wire binding for ease-of-use.

Multi GMP Booklet in english

Get all the relevant GMP's for Pharmaceutical production in one booklet:

• 21 CFR Part 210 (Pharmaceutical production)

• 21 CFR Part 211 (Pharmaceutical production)

• 21 CFR Part 11  (Electronic Records; Electronic Signatures)
• EU GMP guideline, Part I, Ch. 1-9 (Pharmaceutical production)

• EU GMP guideline, Part II, (API, conforms with ICH Guideline, Q7A)

» Sample (pdf)
» Updating policy and current versions

GMP Translations

Translations with the original text in parallel

  » Français

• 21 CFR Part 210 et 211(Pharmaceutiques) » Sample

• 21 CFR Part 820 (Dispositifs Médicaux) » Sample

• EU GMP guide, Partie I, Ch. 1-9 (Pharmaceutiques) » Sample

» EU GMP guide, Partie II, (Pharmaceutiques, PAP) » Sample

  » Svenska

» 21 CFR Part 210, 211 och 11  (Läkemedel samt ER/ES) » Sample

» 21 CFR Part 820 och 11 (Medical Device samt ER/ES) » Sample

» EU GMP guide Part I, kapitel 1-9 (Läkemedel) » Sample

» EU GMP guide, Part II (API-tillverkning. ICH Guideline, Q7) » Sample

  » Dansk

» EU GMP guide, Part I (Lægemiddelfremstilling) » Sample

» EU GMP guide, Part II (API-fremstilling. ICH retningslinjer, Q7) » Sample

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