Aegis Technologies Inc. · Audit and evidence platforms

Four products, one job:
evidence the person asking can check.

An aerospace registrar. An automotive customer. An FDA investigator. A BVLOS regulator or insurer. Each Aegis product reads the records you already keep and turns them into evidence that one person can check, built for that one moment.

  • ® AeroAssure · AS9100D
  • ® AutoAssure · IATF 16949
  • ™MedAssure · ISO 13485 and QMSR
  • SkyAssure · BVLOS operations

The products

Pick the one built for your audit, inspection or flight.

Each card goes to that product's page, with its demo, sample reports and full price list.

Aegis AeroAssure®

Aegis AeroAssure®

AS9100D · Aerospace suppliers

Weeks of AS9100D audit prep, done in less than five business days.

For
Tier 2 and Tier 3 aerospace suppliers and special processors: the quality director and the plant GM.
What you get
An Audit Defense Pack built from the registers you already export: readiness clause by clause, the gauge, supplier or process behind a dozen separate findings, ranked fixes with an owner on each, and the auditor's questions for every gap. The pack is signed, so anyone can check nothing in it changed.
Audit Defense Pack: $3,500 founding priceFive places, list $6,500. Standard Facility subscription from $15,000 a year.
Aegis AutoAssure®

Aegis AutoAssure

IATF 16949 · Automotive suppliers

Hundreds of hours of IATF prep, on your desk in five business days.

For
Tier 2 and Tier 3 automotive supplier plants: the supplier quality manager and the plant manager, before an IATF audit or under an OEM's controlled shipping.
What you get
A pack built from your CAPA and 8D logs, PFMEAs and control plans, PPAP files, gauge studies and supplier scorecards: the part, supplier or gauge behind a run of findings, ranked actions with owners, and a Quarterly Business Review for your GM.
Entry pack: $3,500 founding priceList $5,000. Facility subscription from $10,000 a year. CS1 / CS2 / New Business Hold Exit Sprint: $17,500 fixed.
Aegis MedAssure™

Aegis MedAssure™

ISO 13485 and FDA QMSR · Medical devices

Your QMS records, read clause by clause, with a ranked fix list in five business days.

For
Medical device makers, their contract manufacturers and contract sterilizers: the quality and regulatory lead, before an FDA inspection, an MDSAP or notified-body audit, or an OEM's supplier audit.
What you get
A readiness report against ISO 13485:2016 and the QMSR, every finding tied to the record it came from, the common causes ranked first, and the questions an investigator or auditor is likely to ask.
Entry pack: $7,500 founding priceList $12,500. Facility subscription from $18,000 a year.

MedAssure is not a medical device and makes no clinical or reportability decisions; it reads and organizes the manufacturer's own records.

Aegis SkyAssure

Aegis SkyAssure

BVLOS operations · Drone operators

Evidence for every BVLOS flight: sealed, signed and ready to send.

For
BVLOS drone operators, from small service providers to utilities: the safety or compliance lead, when a regulator, insurer or customer asks to see that a flight met its authorization.
What you get
SkyAssure sits above the flight-log, fleet and dock tools you already use, checks each flight against your authorization's configured requirements, shows missing evidence as missing, and seals the period into a signed package with its own verifier. Requirements evaluated against available evidence; not a determination of legal or regulatory compliance.
Subscriptions from $6,000 a yearStart with a Compliance Readiness Assessment ($12,500–$25,000 by scope; $7,500 for design partners) or an Incident “Prove It” export ($5,000).

Sample reports on each product's site are built from fictional sample companies. No sample company is a customer.

How they work

Different standards. The same three rules.

Your records, as they are

Each product starts from exports and logs you already keep. No new system to adopt before you see a result.

Every result cites its record

Findings point back to the record they came from, and anything the records can't show is stated as a gap, not filled in.

A person signs off

Software does the reading and sorting. A qualified person reviews what goes out, and nothing is presented as a certification.

Not sure which product fits?

Tell us what you need to show and to whom. We'll point you to the right product, or tell you plainly if none of them fits.