1. European Medicines Agency, ICH guideline Q8 ( R2) on pharmaceutical development, 8,2015, pp. 1–24. doi:EMEA/CHMP/167068/2004 - ICH.
2. Process analytical technology for continuous manufacturing of solid-dosage forms;Fonteyne;TrAC - Trends Anal. Chem.,2015
3. European Medicines Agency, Guideline on Real Time Release Testing (formerly Guideline on Parametric Release), 44, 2012, pp. 1–10.
4. European pharmacopoeia. 8th ed. 2014 European Directorate for the Quality of Medicines (EDQM), Council of Europe, Strasbourg, France., (n.d.).
5. Pharmaceutical and Medical Applications of Near-Infrared Spectroscopy;Ciurzak,2002