Welcome to
vpluspharmaaudit
We provide professional advisory and supportive consultancy services in pharmaceutical quality systems and GMP compliance. Our goal is to help organizations strengthen and sustain regulatory compliance through expert guidance.
First Visit FREE
Complimentary first consultation to assess compliance readiness and provide an expert advisory roadmap.
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Our Vision
To be the leading global partner in pharmaceutical compliance, bridging the gap between operational standards and regulatory excellence through high-quality advisory.
Our Mission
Enable pharmaceutical and healthcare organizations to achieve and maintain regulatory compliance through ethical, transparent, and supportive advisory services.
Why Choose vpluspharmaaudit?
We bridge the gap between operational challenges and global regulatory expectations with ethical and supportive advisory.
Global Framework Alignment
Expertise in aligning with USFDA, WHO-Geneva, TGA, MHRA, and ISO standards to ensure your facility is world-class.
Supportive Role Only
We maintain a strictly non-operational role, providing ethical and transparent guidance while you retain 100% control.
Documentation Driven
Focus on audit-ready documentation and process risk assessment to strengthen and sustain regulatory compliance.
Qualified Leadership
Led by experts with M.Sc. Microbiology and M.Pharm backgrounds, bringing years of QA/QC experience to the table.
Send Your Inquiry
Interested in our GMP & ISO consultancy? Reach out to us for expert guidance.
Email: prasadvaidya21@gmail.com
Call: +91 97376 03139
Thanks for reaching out!
We appreciate your interest in vpluspharmaaudit. Our experts will get back to you within 24 hours.
