Manufacturers of medicinal products must be able to document the measures they have taken to ensure that their supplier of excipients complies with good practice under the conditions set out in article L. 5138-3.
Home | French Legislation Articles | Part five: Health products | Book I: Pharmaceutical products | Title II: Medicinal products for human use | Chapter IV: Manufacturing and wholesale distribution | Section 4: Manufacture and import. | Subsection 1: General provisions applicable to manufacture and import. | Article R5124-49-3 of the French Public Health Code
Manufacturers of medicinal products must be able to document the measures they have taken to ensure that their supplier of excipients complies with good practice under the conditions set out in article L. 5138-3.
Les fabricants de médicaments doivent être en mesure de documenter les mesures qu’ils ont prises pour s’assurer du respect, par leur fournisseur d’excipients, des bonnes pratiques dans les conditions prévues à l’article L. 5138-3.
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PETROFF LAW FIRM (SELARL LEGASTRAT)
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75001, Paris France
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is a Registered Trademark of
PETROFF LAW FIRM (SELARL LEGASTRAT)
182, rue de Rivoli
75001, Paris France
RCS Paris n°814433470
Paris Bar Registration n° (Toque) C2396
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