11 - 14 February, 2019 | Meliá, Berlin, Germany
Contact Us: 44 (0) 207 368 9300
Earlier this month Pharma IQ opened up the opportunity for pharma and biotech professionals to submit their burning compliance questions on software for medical devices. Now, the MHRA’s Senior Regulatory Specialist for Devices – Rob Higgins - takes the floor on the subject.
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