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Our Services
Revolutionize Your Drug Development Journey with Intellitron Research's Customizable Services
End-to-End Regulatory Affairs - CoE
The regulatory affairs CoE provides comprehensive solutions to help clients navigate the complex world of regulatory affairs. The team of experts manages regulatory affairs across a wide range of therapeutic areas.
End-to-End Pharmacovigilance - CoE
The pharmacovigilance CoE provides comprehensive solutions for the entire pharmacovigilance process. The team of experts ensures that clients' products are safe for patients, offering a wide range of pharmacovigilance services.
Medical Regulatory Writing
The medical writing team offers a full range of services to meet clients' medical writing needs. The team of expert medical writers delivers high-quality, accurate, and timely medical writing services that meet regulatory requirements
Global Medical Devices RA and PV capabilities:
At the Medical Devices Global Regulatory Affairs and Pharmacovigilance division, the team offers end-to-end solutions to ensure that medical devices comply with regulatory requirements around the world.
End-to-End Quality, Compliance, & Audits - CoE
The quality, compliance, and audits CoE is designed to help life science companies navigate the complex world of quality and compliance. Our team ensures that clients' products and processes meet the highest quality standards and comply with all relevant regulations.
PV/Safety Technology Capabilities
We offer comprehensive capabilities to support your pharmacovigilance and safety technology needs. Our services include PV automation, data migration, E2B parsing, and line listing. We also offer support for Axway and E2B gateways, as well as Argus safety database capabilities and signal application support.