Transcription of BRACKETING AND MATRIXING DESIGNS FOR …
{{id}} {{{paragraph}}}
Example: stock market
BRACKETING AND MATRIXING DESIGNS FOR …
INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE ICH HARMONISED TRIPARTITE GUIDELINE BRACKETING AND MATRIXING DESIGNS FOR stability testing OF NEW drug SUBSTANCES AND PRODUCTS Q1D Current Step 4 version dated 7 February 2002 This Guideline has been developed by the appropriate ICH Expert Working Group and has been subject to consultation by the regulatory parties, in accordance with the ICH Process. At Step 4 of the Process the final draft is recommended for adoption to the regulatory bodies of the European Union, Japan and USA. Q1D Document History First Codification History Date New Codification November 2005 Q1D Approval by the Steering Committee under Step 2 and release for public consultation. 10 November 2000 Q1D Current Step 4 version Q1D Approval by the Steering Committee under Step 4 and recommendation for adoption to the three ICH regulatory bodies.
BRACKETING AND MATRIXING DESIGNS FOR STABILITY TESTING OF NEW DRUG SUBSTANCES AND PRODUCTS ICH Harmonised Tripartite Guidelines Having reached Step 4 of the ICH Steering Committee meeting on 7 February 2002, this guideline is recommended for adoption to the three regulatory parties to ICH
Loading..
Tags:
Information
Domain:
Source:
Link to this page:
Please notify us if you found a problem with this document:
Related search queries
Stability Testing of new Drug, STABILITY TESTING OF NEW DRUG SUBSTANCES AND PRODUCTS, Q1A(R2) Guideline Stability Testing of New, Q1A(R2) Guideline Stability Testing of New Drug Substances and Products, A Stability Testing Guidelines:, Products, Stability Testing of New, Drug Substances, Stability Testing of Pharmaceutical, Stability Testing of Pharmaceutical Products, Stability testing, STABILITY TESTING OF ACTIVE SUBSTANCES, STABILITY TESTING OF ACTIVE SUBSTANCES AND PHARMACEUTICAL PRODUCTS, Stability