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Questions about Valiqa, enterprise pricing, or just want to talk validation? We read every message.


Direct email

Response time

We typically respond within one business day.


Who reaches out and why

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.

Product questions

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.

Enterprise pricing and contracts

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.

Security, privacy, and compliance

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.

Partnerships and integrations

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.

Press, analysts, and industry research

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.

Bug reports and feature requests

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.


What to include in your message

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:

  • Your industry (medical device, pharmaceutical, biotech, food, or other regulated manufacturing)
  • Approximate team size and number of qualifications you run per year
  • Your current tool or process (templates, QMS-with-validation-module, enterprise VLMS, mixed)
  • The specific protocol types you care about (IQ, OQ, PQ, PPQ, CSV, PV, VMP, PFMEA)
  • The regulatory frameworks you operate under (FDA QMSR, ISO 13485, EU MDR, ICH, etc.)
  • Whether you are evaluating, comparing, or have a specific buying timeline

None of this is required. The form will go through regardless. It just helps us calibrate the response.


Response time and what to expect

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.


Before you reach out: a few resources that may answer your question faster

Several common inbound questions are already answered on the site. Pointers, depending on what you came here to ask:

  • Wondering which category of validation tool fits your team? Try our self-scoring tool at /evaluate.
  • Trying to scope which protocols your equipment needs? The protocol selector walks through it in five questions.
  • Want a structured walkthrough of the validation tool landscape? Read our buyer guide.
  • Pricing details and tier comparisons live on the pricing page.
  • Common product questions are answered on the FAQ page.

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