Your Trusted Regulatory Operations Partner
Delivering Tailored Solutions in RIM Systems, Submission
Management, and Process Optimization with Unmatched Efficiency and Expertise.
About US
With over 20 years of experience in the life sciences industry, Votum Consulting is a trusted partner in delivering high-quality regulatory services. We specialize in Regulatory Information Management (RIM) system implementation and oversite, as well as comprehensive document and eCTD submission publishing. Our deep industry expertise enables us to support pharmaceutical, biotechnology, and medical device companies in navigating complex regulatory landscapes with precision and efficiency.
Our Services
We provide expert document formatting and publishing services to ensure regulatory compliance, clarity, and submission readiness for health authority approvals.
We specialize in Regulatory Information Management (RIM) systems, particularly Veeva, helping clients implement tailored solutions that enhance compliance, data integrity, and regulatory efficiency.
We specialize in submission publishing and management, ensuring accurate compilation, formatting, and dispatch to health authorities with ongoing support for a seamless approval process.
We provide continuous RIM system support, ensuring compliance, optimal performance, and proactive issue resolution through regular audits, maintenance, and process improvements.
We provide secure and compliant archiving support for regulatory documents, submissions, and correspondence, ensuring easy retrieval, data protection, and streamlined future submissions.
We create and evaluate SOPs and work instructions to ensure clarity, compliance, and best practices, with regular updates to align with regulatory changes and operational needs.
Contact Us
Interested in working together? Fill out some info and we will be in touch shortly. We can’t wait to hear from you!