Biopharma Medical Writing

we provide regulatory medical writing services for clinical trials, regulatory submissions, pharmacovigilance and translation solutions – pharmaceuticals and medical devices. assuring your company has a consistent and regulatory-compliant documentation across all phases of the product life cycle on time, in a cost-effective manner, making your submission process easy and convenient. we keep up to date with global regulatory requirements (ich, gcp, gvp, isos and ghtf guidelines) as we understand that the way your documents are presented to the regulatory authorities plays a major role when it comes to approval and that any gaps can lead to drastic results. consistency and regulatory compliance is the core of our service, this aligned with a knowledgeable team open to talking and understand your needs and expectations to ensure high quality, on time project deliverables.