Recent Progresses in Analytical Perspectives of Degradation Studies and Impurity Profiling in Pharmaceutical Developments: An Updated Review

Author:

Jahani Maryam1,Fazly Bazzaz Bibi Sedigheh12,Akaberi Maryam3ORCID,Rajabi Omid1,Hadizadeh Farzin234ORCID

Affiliation:

1. Department of Pharmaceutical Control, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran

2. Biotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran

3. Department of Pharmacognosy, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran

4. Department of Medicinal Chemistry, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran

Publisher

Informa UK Limited

Subject

Analytical Chemistry

Reference158 articles.

1. International Conference on Harmonisation (ICH), Impurities in New Drug Products Q3B (R2), IFPMA, Geneva (Switzerland), 2006.

2. International Conference on Harmonisation (ICH), Impurities in New Drug Substances Q3A (R2) IFPMA, Geneva (Switzerland), 2006.

3. International Conference on Harmonisation (ICH), Stability Testing of New Drug Substances and Products Q1A (R2) (Revised Guideline), 2003.

4. International Conference on Harmonisation (ICH), Photostability Testing of New Drug Substances and Products ICH Q1B, 1999.

5. International Conference on Harmonisation (ICH), Stability Testing for New Dosage Forms ICH Q1C, 1997.

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