Signed in as:
filler@godaddy.com
Signed in as:
filler@godaddy.com
We provide services for authoring CSRs (full, synoptic and abbreviated) across all the phases of clinical study compliant with the ICH GCP guidelines
Clinical and non-clinical module documents including summary documents, ISE, ISS, Overview documents, etc.
Research protocols and amendments
IBs and IB updates
Patient safety narratives for inclusion in Clinical Study Report
Our specialized team in Europe author medical device documents and related technical documents including CERs, post market documentations (PSURs, and PBRERS), Risk Management documents, service manuals etc.
Including PSURs, PADERs, Patient Information Leaflets, individual case safety reports, etc.
Quality control of all regulatory documents
Our team comprises of qualified professionals with specialized experiences in field of medical writing who can help you achieve your goals efficiently without compromising the quality..
Our team comprises of professionals with Masters to Doctorate level of education.
We are experts in writing both pharmaceuticals and medical device documents across all phases of clinical study in various therapeutic areas
We strictly comply with the ICH-GCP guidelines and other regulatory guidelines for US and Europe countries.
We provide services that are tailored and personalized according to the client needs and requirements.
We help you attain your goals in cost-effective manner
Copyright © 2023 CogniScribe Services - All Rights Reserved.
Powered by GoDaddy
We use cookies to analyze website traffic and optimize your website experience. By accepting our use of cookies, your data will be aggregated with all other user data.