11. January 2017 Abstract With the implementation of quality by design (QbD), critical attributes of raw material (drug substance and excipients) are of significantly…

17. November 2016 Abstract This study aimed to apply quality risk management based on the The International Conference on Harmonisation guideline Q9 for the early…

15. November 2016 Are you interested in an alternative source complying with EP/USP-NF/JP monographs, US FDA DMF, CEP from a cGMP facility? Get in touch with:…

24. October 2016 Abstract The rapidly growing medical expense going with aging population in Japan requires the use of generic products derived from off-patent active…

26. September 2016 CPhI Worldwide, organized by UBM EMEA, has announced the findings of part i of the 2016 CPhI Annual Report on potential new approaches to improve quality and manufacturing process in pharmaceutical…

25. July 2016 Abstract The feasibility of a colorimetric technique was investigated in CIELAB color space as an analytical quality control method for content uniformity…

04. July 2016 Context: Orodispersible films have gained increasing relevance as a novel dosage form. Associated to their particular processing and multicomponent…