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Melkor ☆ Greece, 2015-10-11 21:49 (3907 d 20:45 ago) Posting: # 15551 Views: 2,962 |
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Greetings, I was wondering what are the requirements for a variation in MHRA for change of FDF manufacturer for a oral liquid product. I guess that a process validation is essential is it though also a minimum stability data required in order to proceed with the submission of the variation? Thank you ![]() |

