Virtual Facility Inspections

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Virtual Facility Inspections

At Isha’s GMP Consultancy, we provide Virtual Facility Inspections to help pharmaceutical, biotechnology, and healthcare companies ensure GMP compliance, pre-approval readiness, and regulatory adherence.

Why Virtual Inspections Matter?

A facility inspection—whether GMP, pre-approval, or routine compliance—is a critical step in the drug approval process. Our team of former senior FDA managers, industry experts, and compliance specialists ensures that your facility meets global regulatory requirements through a remote, technology-driven approach.

Our Virtual Inspection Process:

  • Pre-Inspection Readiness Assessment – Identify gaps and compliance risks
  • Document & Data Review – Ensure all records align with regulatory expectations
  • Live Virtual Walkthroughs – Real-time facility inspections with experts
  • Audit Preparedness Training – Simulated inspections to prepare teams
  • Regulatory Compliance Guidance – Expert insights based on FDA, EMA, WHO, and other standards
  • Corrective & Preventive Actions (CAPA) – Assistance in resolving compliance issues

Cutting-Edge Virtual Inspection Technology

We utilize advanced remote inspection tools to provide an immersive and interactive experience, ensuring thorough compliance assessments without the need for on-site visits.

With Isha’s GMP Consultancy, you can navigate FDA, EMA, MHRA, and WHO inspections efficiently, minimizing delays and ensuring regulatory approval success.

FDA Services