Are you a CMC manager, regulatory affairs manager or a manager of the quality assurance department dealing with the compilation and the maintenance of the Module 3 of the CTD, classification of quality-related changes? FORUM • Institut für Management organizes the course “CMC Management in Regulatory Affairs – Quality data for marketing authorisation in Europe”, […]
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Are you working in regulatory affairs or in related departments that need essential European regulatory affairs expertise? Do you need essential European regulatory affairs knowledge? FORUM • Institut für Management organizes the course “Marketing authorisation in Europe for beginners” (19-21 November 2018 in Amsterdam) will inform you about all the important obligations and challenges in […]
The promotion of pharmaceutical products is strictly regulated on a national level. DADA provides compliance control of promotional activities in the BeNeLux, and as such acts as a Scientific Service. The compliance review is conducted as per the applicable legislation or self-regulation; BeNeLux laws and Codes of Conduct, where necessary complemented by the EFPIA Code or EU […]
DADA CONSULTANCY B.V. (www.dada.nl), is a leading, independent and international consultancy in the field of development, registration and quality control of medicines (human and veterinary). DADA is located in a modern office building in Nijmegen and Poland. You will work in a young and enthusiastic team of 26 employees. DADA is characterized by its high […]
DADA Consultancy is a highly specialised and independent consultancy agency in international regulatory affairs of human and veterinary medicinal products.
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