Third Party Audit & Compliance Consultant | Isha’s GMP Consultancy
Isha’s GMP Consultancy — leading Third Party Audit & Compliance Consultant for pharma, biotech & food industries. Expert in GMP audits, gap analysis, and compliance documentation.
Third Party Audit & Compliance Consultant
As a trusted Third Party Audit & Compliance Consultant, Isha’s GMP Consultancy helps organizations maintain regulatory excellence and ensure continuous compliance with GMP, WHO, EU, and USFDA standards. With over 15 years of hands-on experience, we conduct independent audits, identify process gaps, and assist in closing non-conformities before official inspections.
Our expertise as a Third Party Audit & Compliance Consultant extends across pharmaceutical, biotechnology, cosmetic, nutraceutical, and food processing industries. We provide unbiased assessments, internal audit support, and audit readiness programs to strengthen your quality systems. Whether you need a pre-audit review, supplier qualification audit, or full GMP compliance evaluation, Isha’s GMP is the Third Party Audit & Compliance Consultant you can depend on.
Our Third Party audit & Compliance consultant Services
As an experienced Third Party Audit & Compliance Consultant, we offer end-to-end services that ensure your facility meets international standards and passes audits confidently:
- GMP, WHO, FDA, EU & ISO Compliance Audits
- Internal and External Third-Party Audits
- Supplier Qualification & Vendor Audits
- Gap Analysis & Corrective Action Plans (CAPA)
- Regulatory Documentation Review & Support
- Pre-Inspection Readiness Programs
- Mock Inspections & Risk Assessments
- Data Integrity & QMS Compliance Checks
- Audit Training & Quality System Upgrades
- Continuous Monitoring & Post-Audit Support
Every audit is led by certified experts who combine technical know-how and compliance insight to deliver detailed, actionable audit reports. Our role as your Third Party Audit & Compliance Consultant is to ensure that every process, document, and system is aligned with the latest international regulatory requirements.
Past Audit & Compliance Projects
Case Study 1: GMP Audit & Compliance Review – Hyderabad
Client: API Manufacturer
Scope: Full-scale third-party GMP audit, gap analysis, and corrective implementation plan.
Outcome: Client achieved WHO-GMP recertification within 8 months and improved internal documentation systems.
Case Study 2: Compliance Audit – Chennai Biotech Facility
Client: Biotechnology Startup
Scope: Supplier audit, equipment qualification checks, and CAPA documentation.
Outcome: The facility cleared EU audit with zero major non-conformities.
What Our Clients Say
“Isha’s GMP team conducted a detailed third-party audit that helped us prepare for our WHO inspection. Their reports were precise, practical, and solution-driven.”
– Dr. Anil K., QA Head, Pharma Manufacturing Unit
“Professional and reliable. As a Third Party Audit & Compliance Consultant, Isha’s GMP helped us close compliance gaps and train our QA team effectively.”
– Neha R., Regulatory Affairs Manager, Biotech Company
Frequently Asked Questions (FAQs)
A Third Party Audit & Compliance Consultant independently reviews your facility, documentation, and systems to identify gaps and ensure compliance with GMP and regulatory standards.
Working with a Third Party Audit & Compliance Consultant gives you an unbiased view of your operations and prepares your organization for regulatory inspections.
As an expert Third Party Audit & Compliance Consultant, we handle GMP, supplier, quality system, and data integrity audits across multiple industries.
Yes. Our Third Party Audit & Compliance Consultant team offers mock inspections, documentation reviews, and CAPA guidance to ensure readiness.
Absolutely. As your Third Party Audit & Compliance Consultant, we assist in implementing corrective actions and updating QMS systems for sustained compliance.