Questions about Valiqa, enterprise pricing, or just want to talk validation? We read every message.
We typically respond within one business day.
Valiqa works with validation engineers, quality managers, regulatory affairs leads, and engineering teams across medical device, pharmaceutical, biotech, and regulated food manufacturing. The team behind this product reads every inbound message. Here is what people typically write in about.
How Valiqa handles a specific protocol type, whether a regulatory framework is supported, how the export format renders for a particular jurisdiction, integration questions, or anything you want to confirm before starting a trial. We answer with specifics, not marketing copy. If a feature is not implemented, we say so.
Custom plans for teams beyond the published Business tier, multi-site licensing, procurement requirements, security questionnaires, SOC 2 inquiries, and contract review. Reach out at [email protected] directly if your procurement timeline is tight.
Questions about our security posture, data handling, field-level encryption, audit trail behavior, 21 CFR Part 11 alignment, or our privacy practices. Coordinated vulnerability disclosures are welcomed at [email protected]. We will work with you in good faith and acknowledge the report promptly.
QMS vendors, document management platforms, training systems, and adjacent tools where an integration would help mutual customers. We are selective but always interested in genuine fits.
Interviews, expert commentary on validation, regulatory framework questions, or analyst briefings. The team behind Valiqa has hands-on validation engineering experience in regulated manufacturing and is willing to go on record.
We take both seriously. The fastest way to get a bug fixed is to include the steps to reproduce, the expected vs actual behavior, and any relevant context (browser, equipment context, protocol type). Feature requests get reviewed weekly.
You do not have to follow a template. A short note is fine. If you want the fastest, most useful response, including some of the following helps us reply with substance rather than asking follow-up questions:
None of this is required. The form will go through regardless. It just helps us calibrate the response.
We aim to respond within one business day for general inquiries, and faster for product questions from teams in active trial. Enterprise procurement and security review timelines vary depending on the scope; we will tell you upfront what is realistic for your engagement.
Messages tagged as urgent because of a production blocker get prioritized. If Valiqa is in your validation workflow and something is broken, write "Production blocker" in the subject line.
If you have not heard back within two business days for general inquiries or within four hours for a production blocker during business hours, follow up at [email protected] in case the form submission ran into a delivery issue.
Several common inbound questions are already answered on the site. Pointers, depending on what you came here to ask:
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