Would you like SIMPLIFIED & FASTER Dossier Submissions?
Welcome to Dyaz Innovate! We are a forward-thinking software startup dedicated to revolutionizing the way regulatory processes are managed within the pharmaceutical industry.
Our flagship product DyazRIMS™ is a comprehensive web-based regulatory affairs platform designed to simplify document preparation, eCTD publishing, and regional validations. With our intuitive online interface, regulatory professionals can manage workflows from anywhere, streamline submissions, reduce errors, and ensure timely regulatory compliance.
Alongside DyazRIMS™, we offer DyazCTD — a robust desktop application built specifically for managing structured CTD formats. DyazCTD enables regulatory teams to create region-specific CTD structures, automate Table of Content (TOC) generation, and manage submissions seamlessly. With features like template creation, document management, CTD regional structuring, submission tracking, query management, and local storage, DyazCTD ensures fast, secure, and compliant CTD preparation.
What sets us apart is our commitment to innovation and customer satisfaction. We continuously strive to stay ahead of industry trends and regulatory changes, integrating the latest advancements in technology to enhance our software and provide unparalleled value to our clients.
At Dyaz, we believe in fostering strong partnerships with our customers. We work closely with regulatory teams to understand their unique needs and challenges, offering personalized support and tailored solutions to help them achieve their goals efficiently and effectively.
our mission to transform regulatory affairs. Together, we can navigate the complexities of compliance and empower the pharmaceutical industry to bring innovative products to market faster, while ensuring the highest standards of safety and efficacy.
We combine innovation and compliance to redefine how regulatory submissions are managed. Our integrated tools handle everything — from document structuring and cloud storage to validation reporting — ensuring a seamless, error-free workflow.
Configure regional templates once and reuse them seamlessly across submissions.
Maintain an accurate folder structure throughout every submission lifecycle.
Preserve all document versions securely with sequence-based cloud storage.
Convert DOCX files to PDF effortlessly before proceeding with eCTD publishing.
Auto-generate regional and submission XML files compliant with eCTD v3.2.2.
Upload or download ZIP sequences with ease for complete submission control.
Validate sequences with global criteria — USFDA, EMA, GCC, ECOWAS, SAHPRA.
Track every document from draft to submission in a centralized, controlled workflow.
Generate detailed, crisp reports tracing every validation for complete accuracy.
Choose the right option for your regulatory publishing and document management needs — scalable, secure, and tailored for every organization.
A smarter way to manage regulatory workflows with automated templates, submission tracking, and document control — all in one place.
Streamline your regulatory publishing with structured CTD formats, regional compliance, and seamless submissions for global markets.
Getting started with DyazRIMS™ is simple and seamless. Our streamlined process ensures you experience the platform’s full capabilities with ease and confidence.
Pre-build eCTD Structure Smart & Reusable Content
OneDrive Integration Convert DOC to PDF.
Agency ready Sequence & Backbone files.
USFDA, EMA, GCC, ECOWAS, SAHPRA* Download Validation Report.
Download & Upload Sequence ZIP file
Targeted Customer Satisfaction
Faster Dossier Preparation
Expected Business Growth
Simplify document creation, collaboration, and approval processes.
Ensure version control and traceability for all regulatory documents.
Facilitate seamless integration with existing enterprise systems.
Accelerate the submission process with efficient electronic Common Technical Document (eCTD) publishing.
Ensure compliance with global regulatory standards for electronic submissions.
Streamline the compilation, validation, and lifecycle management of eCTD dossiers.
Validate sequences against validation criteria defined by respective regional agencies (USFDA, EMA, GCC, ICH, SAHPRA, etc.).
Ensure data integrity and accuracy throughout the regulatory lifecycle.
Expedite the validation process to meet regulatory timelines effectively.
Focus on your regulatory goals, and let DyazRIMS™ simplify the compliance process for you.
Register for a free demo or Talk to us