We ensure that your quality system complies with the Good Manufacturing Practices (GMP) and perform the batch certification.
Make use of our expertise and experience as RP for a pragmatic quality system, compliant with the Good Distribution Practices (GDP).
Your advertising and interactions with health care professionals are safe in the hands of our Responsible Person for Information & Publicity (RIP).
Regulatory Affairs (RA)
We assist you in the development of your regulatory strategy, by monitoring your development projects and modification of your registration files, and during all interactions with the authorities.
Q-support can act as your local point of contact for pharmacovigilance in Benelux.
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