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Tell us the audit or filing you're facing. We'll tell you who should run it.

Whether it's a single-site GMP audit or an ongoing third-party audit programme across several markets, share your scope and timeline and a member of our consulting team will respond directly.

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Get In TouchHave questions or need assistance? We're here to help.

Fill out the form and a member of our consulting team will get back to you shortly - or reach us directly below.

Phone
+91 6352 795 864Mon–Sat, 9:00–18:00 IST
Email
Info@Pharmacompliancerx.ComReplies within one business day
Office
Ahmedabad, IndiaConsultant network positioned across 30+ countries

Global ReachHeadquartered in Ahmedabad, working across 30+ countries

Our consultant panel is positioned regionally so an audit reads as locally credible wherever your site sits.

Headquarters

India

Ahmedabad — core operations, client coordination and consultant scheduling.

Consultant Coverage

North America

Site audits and regulatory support aligned to FDA expectations.

Consultant Coverage

Europe

EU-GMP audits and dossier support across major regulatory markets.

Consultant Coverage

Wide Range of Services

One partner for GMP audits, regulatory filings, and the quality systems that keep you inspection-ready.

Before You Reach OutCommon questions

If your question isn't answered here, the fastest route is still the form above — tell us your scope and we'll follow up directly.

How quickly can a consultant be assigned to an audit?

For most engagements we can confirm a matched consultant within a few business days of receiving your regulatory scope, site location and target timeline. Complex multi-country programmes may take longer to staff correctly.

Yes. We run both, and will recommend the right format based on your regulatory scope, site risk profile and travel constraints.

Our consultant panel works to FDA, EU-GMP and WHO expectations, and can align to local-authority requirements in the markets covered by our 30+ country network.

Yes, this is one of our core service lines. We can run a recurring supplier or site qualification programme with consistent reporting standards across every location.

We track any resulting CAPAs through to close-out and keep the file on record, so it's ready to hand to your next inspector without additional preparation.