FAQs

Voyantix Technologies is a Hyderabad-based software company that builds enterprise quality, compliance, and operational platforms for life science organizations. Our product suite covers QMS, LMS, DMS, LIMS, HRMS, and EMS — all designed to meet GxP regulatory requirements such as FDA 21 CFR Part 11 and EU Annex 11.

Voyantix serves pharmaceutical companies, biotech organizations, medical device manufacturers, CROs, contract manufacturing organizations, and other life science enterprises that operate in GxP-regulated environments.

Voyantix Technologies is headquartered in Hyderabad, Telangana, India, and serves life science clients worldwide.

You can reach Voyantix by emailing info@voyantixtech.com, submitting the contact form on our website, or booking a demo through our contact page. Our team typically responds within one business day.

Voyantix offers six integrated products: QMS (Quality Management System), LMS (Learning Management System), DMS (Document Management System), LIMS (Laboratory Information Management System), HRMS (Human Resource Management System), and EMS (Environmental Monitoring System). Together they form a unified compliance and operations platform for life science organizations.

Yes. You can start with one product module and expand to additional products as your needs grow. Pricing and packaging are tailored to your organization's scope, user count, and regulatory requirements.

QMS manages quality events such as deviations, CAPA, change control, audits, and risk. LMS delivers and tracks GxP training with competency assessments. DMS controls documents with versioning, approval workflows, and electronic signatures. LIMS manages laboratory samples, tests, and results. HRMS handles personnel records, onboarding, and employee data. EMS monitors environmental conditions such as temperature, humidity, and cleanroom parameters.

Yes. Voyantix supports integration with ERP systems, LIMS, instrument middleware, authentication providers, and other enterprise tools through secure APIs and industry-standard protocols. Our team works with you to design integrations that fit your IT landscape.

Yes. Voyantix platforms are designed and validated to support FDA 21 CFR Part 11 requirements for electronic records and electronic signatures, including access controls, audit trails, electronic signature workflows, and system validation documentation.

The Voyantix validation package includes risk assessments, user requirement specifications, functional design specifications, validation test scripts, traceability matrices, and validation summary reports. These documents help your quality organization demonstrate system suitability during audits and inspections.

Yes. Voyantix platforms are designed to support EU GMP Annex 11 requirements for computerized systems, covering data integrity, access management, audit trails, electronic signatures, data storage, and incident handling.

Voyantix enforces data integrity through ALCOA+ principles — records must be attributable, legible, contemporaneous, original, and accurate, along with complete, consistent, enduring, and available. Role-based access controls, immutable audit trails, electronic signatures, and secure backups protect your regulated data throughout its lifecycle.

Pricing depends on the products you select, the number of users, deployment model, and implementation scope. Voyantix offers flexible annual subscription pricing based on modules and user counts. Contact us for a tailored quote based on your organization's requirements.

Typical implementations run 6 to 12 weeks for a single product module, depending on configuration complexity, validation requirements, and data migration needs. Multi-product enterprise rollouts are phased over a longer timeline. A detailed project plan is provided after discovery.

Yes. Voyantix offers guided demonstrations and proof-of-concept evaluations so your team can see the platform in action, test key workflows, and evaluate fit before committing to a full implementation.

Yes. We regularly sign mutual non-disclosure agreements before demos and deeper technical discussions. Contact us and we will provide an NDA template or countersign yours.

Voyantix operates with SOC 2 Type II controls and aligns its information security practices with ISO 27001 principles. Our platforms implement encryption in transit and at rest, role-based access control, continuous monitoring, and regular security assessments.

Voyantix platforms are hosted on enterprise-grade cloud infrastructure with data residency options to meet regional regulatory requirements. Encryption, redundancy, and backup procedures protect data across all environments.

Yes. Voyantix supports single sign-on (SSO) integration with common identity providers using SAML and OpenID Connect, enabling centralized user management, multi-factor authentication, and streamlined access for your workforce.