GMP Audits · Since 2023 · Ahmedabad, India
Audit-ready quality, verified across every market you serve.
Pharma Compliance RX supports pharmaceutical companies globally with GMP audits, third-party audit reports, regulatory filings and quality systems — delivered by consultants with 12 to 35 years of specialist experience.
Why pharmaceutical teams work with us
Consultants and auditors positioned globally, so quality standards read consistently to regulators wherever your operations are.
01
Global Experience
Consultants located worldwide deliver work that reads as credible to regulators and experts internationally.
02
Cost-Effective Rates
A distributed consultant network keeps engagement costs efficient without compromising audit rigor.
03
Flexibility & Timely Delivery
Engagements scale to your timeline, from a single site audit to a multi-country compliance programme.
04
Wide Range of Services
One partner for GMP audits, regulatory filings, and the quality systems that keep you inspection-ready.
OUR AUDITING SERVICES Comprehensive GxP Auditing Services
Conducting GMP
Auditing Services Worldwide
We conduct high-standard GMP audits worldwide across diverse suppliers in accordance with EU GMP, ICH Q7, 21 CFR 210/211, ISO and other applicable standards.
Audits can be fully tailor-made to meet specific customer requirements, including focused areas, products, systems, criticality or for-cause investigations.
Our detailed audit reports are widely accepted by regulators, QPs and subject matter experts globally.
Other GxP
Audits
We provide comprehensive GxP auditing services worldwide, including GCP, GDP, GLP, GPvP and Medical Device audits in accordance with ISO 13485 requirements.
Our highly qualified auditors and subject matter experts conduct audits according to relevant national and international requirements.
Clients can select the most suitable auditor and review the detailed report before finalization to ensure alignment with their internal requirements.
Quality GMP
Auditing Services
Our Quality GMP Auditing Services cover the complete audit lifecycle, from initial supplier coordination through delivery of the final Audit Report.
- Pre-Audit Preparation
- Audit arrangements, travel planning and bookings
- Audit conducting and summary reporting
- Detailed Audit Final Report
- CAPA management and follow-up
- Audit closure and follow-up audit after every three years
Our Mission & VisionSupporting pharmaceutical companies globally, sustainably, and to the highest quality standard
The prime purpose of Pharma Compliance RX is to support pharmaceutical companies globally and remain sustainable by providing services that meet the highest quality standards in an efficient manner.
Pharma Compliance RX has proven its expertise and service to over 150 clients in more than 30 countries. Every consultant, auditor and subject matter expert brings 12 to 35 years of core experience in their area of specialisation.
- Regulator-acceptable quality of work, wherever you operate
- Highly qualified consultants and subject matter experts
- Integral, partnership-led engagement model
150+
New Clients Onboarded
30+
Countries Audited In
35
Years, Top Consultant Expertise
4
Core Service Lines
Our Approach
We have the most complete audit
reports
We work as an integral part of your organization to deliver reports your quality and regulatory teams can act on immediately.
Scope the audit
We align on regulatory framework, site scope and timeline before a single consultant is deployed.
Deploy the right expert
An auditor with matching therapeutic and regulatory experience is assigned from our global network.
Audit & document findings
On-site or remote assessment against GMP, with findings recorded to a standard regulators recognise.
Report, CAPA & close-out
A complete audit report with CAPA tracking through to closure, kept on file for your next inspection.