TACPAS Global delivers independent PV Audits, Clinical Research Training, and specialized Recruitment for pharmaceutical and CRO organizations across India and globally — from our base in Lucknow.
Life Sciences Excellence
Established in 2021 and headquartered in Lucknow, India, TACPAS Global supports pharmaceutical, biotechnology, and healthcare companies in achieving regulatory compliance and operational excellence.
Our team brings 5+ years of industry experience across Pharmacovigilance, Clinical Research, Quality Assurance, and CSV — delivering real-world solutions that protect patient safety and meet global regulatory expectations.
To provide practical, high-quality, and cost-effective compliance solutions that help organizations protect patient safety while meeting global regulatory expectations.
Independent, risk-based audit services tailored for pharmaceutical, biotech, and CRO organizations globally.
Independent and risk-based PV audits assessing compliance with ICH, EMA, and FDA regulatory requirements.
Helping sponsors ensure full GCP compliance and protocol adherence through structured site audit programs.
Assessment of computerized systems in regulated environments ensuring data integrity and compliance readiness.
Industry-focused certifications for life sciences professionals at every stage. Full brochures with fees, schedule, and delivery format are shared on request.
A foundational course covering drug safety principles, adverse event reporting, MedDRA coding, and career pathways in Pharmacovigilance.
Advanced training for experienced PV professionals seeking deep expertise in PSUR, PBRER, DSUR, and benefit-risk assessment.
Comprehensive training covering the full clinical trial lifecycle — from ICH-GCP guidelines to monitoring visits, CTMS, and inspection readiness.
Practical audit training for QA and PV professionals — covering planning, execution, interview techniques, report writing, and risk-based CAPA management.
End-to-end training on investigator site audit methodology aligned with GCP fundamentals and full inspection readiness best practices.
Connecting pharma and CRO organizations with qualified Drug Safety and Clinical Research professionals across India and globally.
Pre-screened PV & Clinical Research professionals at all levels
Technical assessments designed by domain experts
Streamlined shortlisting to reduce your time-to-hire
Flexible models designed to fit your budget
We go beyond identifying gaps — we partner with clients to implement sustainable, practical improvements that withstand regulatory scrutiny.
Objective, unbiased audit findings giving a true picture of your compliance standing.
Prioritized programs focused on areas of greatest regulatory and patient safety significance.
Actionable CAPA guidance grounded in real-world regulatory practice.
Deep expertise across ICH, EMA, FDA, CDSCO, and other major frameworks.
Years of combined expertise in PV, QA & Clinical Research
Audit experience across multiple regions
Certification programs offered
Audit methodology aligned with ICH & international best practices
Partner with TACPAS Global for expert-led pharmacovigilance audits, training, and talent solutions.
For audit support, training enquiries, brochure requests, or recruitment — our team is ready to help.
Vikrant Khand, Gomti Nagar
Lucknow, Uttar Pradesh, India
Monday – Friday | 9:00 AM – 6:00 PM IST
Lucknow, Uttar Pradesh, India
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