We offer a full range of regulatory affairs consultancy services within the EU. Medical writing, CMC & Manufacturing, Registration strategy, Regulatory compliance and more.
We help you to ensure compliance with the regulations as well as maintain your pharmacovigilance activities.
Looking for a suitable eCTD software? eCTD Editor is the right software for you. We can help you with your eCTD submission.
We also provide broad range of services for medical device certification.
Are you looking for effective in-house training tailored to your specific needs in term of registration procedures, preparation of registration dossiers and much more?