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Auravea Healthcare Pharmatech LLP

Auravea Healthcare Pharmatech LLP — Ahmedabad, India

Precision in every process. Compliance in every record.

Paperless calibration and validation, equipment qualification, and the culture media, instruments and PUPSIT systems that keep regulated laboratories compliant.

  • EU GMP Annex 1
  • 21 CFR Part 11
  • ISO 11133
  • GAMP5
A sanitary pressure gauge mounted on stainless steel process equipment
Calibration & Validation

What we do

Three services, one quality system

Calibration and validation, equipment qualification, and laboratory solutions — held to the same standards, documented the same way, delivered by the same team.

  • 01

    Calibration & Validation

    Paperless, 21 CFR Part 11 compliant calibration and thermal mapping — digitally signed certificates, instantly accessible on a cloud-based portal.

    • Thermal calibration (temperature & RH)
    • Mechanical & pressure metrology
    • Traceable standards & uncertainty budgets
    Explore calibration
  • 02

    Equipment Qualification & Testing

    Full-lifecycle IQ/OQ/PQ for temperature-controlled equipment, plus the specialized testing that keeps facilities audit-ready for USFDA, WHO and EU GMP.

    • Thermal mapping & HVAC validation
    • Pure steam quality testing
    • 3D/4D smoke studies for aseptic areas
    Explore qualification
  • 03

    Lab Solutions

    Grade A-manufactured culture media, 50+ instrument models across 8 categories, and PUPSIT systems for EU GMP Annex 1 — one supplier, one quality system.

    • Culture media, ISO 11133 compliant
    • Instruments, 21 CFR Part 11 ready
    • PUPSIT equipment for Annex 1 §8.87
    Explore lab solutions
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Batch Traceability

PUPSIT Equipment

The gold standard of sterile filtration assurance

Pre-use post-sterilization integrity testing verifies the sterilizing filter, its housing and every connection — after sterilization, before any product is committed.

  • EU GMP Annex 1 §8.87
  • 21 CFR Part 11
  • Pharmexpert Solution
Explore PUPSIT equipment

The compliant sequence

  1. Step 01

    Sterilize

    Testing after sterilization is what makes it compliant

  2. Step 02

    Wetting

  3. Step 03

    Pre-use IT

  4. Step 04

    Filtration

  5. Step 05

    Post-use IT

Also from Auravea

Manufacturing divisions

Alongside our services, three product divisions run under the same quality system: pharmaceuticals & APIs, cosmetics, and nutraceuticals.

All divisions
  • Pharmaceutical production line with sealed vials on a stainless steel conveyor

    Pharmaceutical & API

    High-quality APIs engineered for global standards, safety, and therapeutic impact.

    Explore Pharmaceutical & API
  • Amber serum bottle and skincare jars arranged on a pale surface

    Cosmetics

    Science-led skincare solutions crafted for safety, purity, and daily wellness.

    Explore Cosmetics
  • Nutraceutical capsules and supplement gummies displayed on a light background

    Nutraceuticals

    Nutraceuticals designed for daily vitality, preventive care, and holistic wellness.

    Explore Nutraceuticals
A quality-control analyst working at a laboratory microscope

Get to know us

Science, precision and compliance — under one roof

Auravea Healthcare Pharmatech LLP exists to keep regulated science defensible. We deliver calibration, validation and equipment qualification backed by internationally traceable standards, and supply the culture media, instruments and PUPSIT systems that laboratories depend on — serving pharmaceutical, biotechnology, food, beverage and FMCG clients in domestic and international markets.

Audit-Ready by Default

Paperless records, digital signatures and documentation prepared for the inspection

One Quality System

Services, laboratory supply and manufacturing held to the same standards

More about Auravea

How we deliver

From first protocol to final report

Three stages, run by teams that stay involved from one to the next.

  1. 01
    A specialist completing protocol documents with a pen

    Scope & Protocol Design

    Risk-based protocols and study designs aligned with current regulatory expectations.

  2. 02
    A laboratory analyst pipetting a sample at the bench

    Execution & Documentation

    Automated, paperless execution with built-in validations and complete traceability.

  3. 03
    A laptop showing an analytics dashboard of study results

    Reporting & Support

    Audit-ready reports, instant digital access, and support through every investigation.

Customer reviews

What our customers say

Our customers trust Auravea for consistent quality, compliant documentation, and reliable support across services, laboratory supply and manufacturing.

I’m impressed with their skincare formulations. Safe, natural, and effective — Auravea helped us build a brand customers love.

Priya SharmaSkincare

Blog posts

Latest news & articles

Notes from our validation, laboratory and quality teams.

Read all articles

Tell us what your facility has to prove.

Send us a specification, a brief, or a question. Our team replies within one business day.

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