Transcription of ICH Topic Q 1 A Stability Testing Guidelines: Stability ...
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The European Agency for the Evaluation of Medicinal Products Human Medicines Evaluation Unit CPMP/ICH/380/95. ICH Topic Q 1 A. Stability Testing Guidelines: Stability Testing of New Drug Substances and Products Step 5. NOTE FOR GUIDANCE ON Stability Testing : Stability . Testing OF NEW DRUG SUBSTANCES AND PRODUCTS. (CPMP/ICH/380/95). [This guideline replaces relevant section of previous guideline]. APPROVAL BY CPMP December 1993. STUDIES CAN BE SUBMITTED ACCORDING TO THIS GUIDELINE January 1994. DATE FOR COMING INTO OPERATION 1 January 1998. (DOSSIERS SUBMITTED AFTER).
STABILITY TESTING OF NEW DRUG SUBSTANCES AND PRODUCTS ICH Harmonised Tripartite Guideline [EMEA Status as of December 1993] Preamble The following guideline sets out the stability testing requirement for a Registration Application within the three areas of the EC, Japan and the USA. It does not seek necessarily
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Q1C Stability Testing: Requirements for New Dosage, STABILITY TESTING: REQUIREMENTS FOR NEW DOSAGE, STABILITY TESTING OF NEW, Stability, Q5C Stability testing of Biotechnological / Biological, Q5C - Stability testing of Biotechnological / Biological products, Stability testing, Testing, STABILITY TESTING OF ACTIVE SUBSTANCES AND