TACPAS Global delivers independent PV Audits, Clinical Research Training, and specialized Recruitment for pharmaceutical and CRO organizations across India and globally.
Established in 2021 and headquartered in Gorakhpur, Uttar Pradesh, 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.
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-aligned certification programs for fresh graduates, experienced professionals, and career-changers in life sciences.
Foundational pharmacovigilance training covering ICSR processing for fresh graduates and life science professionals entering the drug safety field.
Schedule, fees & format on request.
Advanced training for experienced PV professionals seeking deep expertise in PSUR, PBRER, DSUR, and benefit-risk assessment.
Schedule, fees & format on request.
Comprehensive training covering the full clinical trial lifecycle — from ICH-GCP guidelines to monitoring visits, CTMS, and inspection readiness.
Schedule, fees & format on request.
Practical audit training for QA and PV professionals — covering planning, execution, interview techniques, report writing, and risk-based CAPA management.
Schedule, fees & format on request.
End-to-end training on investigator site audit methodology aligned with GCP fundamentals and full inspection readiness best practices.
Schedule, fees & format on request.
Connecting pharma and CRO organizations with qualified Drug Safety and Clinical Research professionals across India and globally.
Deep expertise in PV, clinical research, and QA talent pools.
Efficient screening and placement for critical regulatory roles.
Pan-India placements with global pharma and CRO clients.
ICSR processing, signal management, case narratives
PV system oversight, regulatory strategy
Clinical case review, benefit-risk evaluation
PSUR, PBRER, DSUR writing & submission
PV audit, CAPA management, compliance
Site monitoring, clinical operations
We bring deep domain expertise, practical experience, and client-first values to every engagement.
Our audits are tailored to your organization's risk profile, focusing effort where it matters most for regulatory compliance.
Comprehensive knowledge of ICH, EMA, MHRA, FDA, and CDSCO requirements to support international operations.
Industry-aligned certifications bridging the gap between academic knowledge and real-world regulatory practice.
We adapt to your timelines, constraints, and business objectives — delivering practical recommendations, not just reports.
Exclusive focus on life sciences means we understand your environment, terminology, and regulatory expectations deeply.
5+ years of hands-on experience in PV, clinical research, and quality assurance — from auditing to training delivery.
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.
Your enquiry has been received. Our team will respond within 1 business day.
Last updated: January 2025
We collect information you provide directly to us, including name, email address, phone number, and any other information you provide through our contact form.
We use the information collected to respond to your enquiries, provide our services, and communicate with you about our training programs, audit services, and recruitment solutions.
We do not sell, trade, or otherwise transfer your personal information to third parties without your consent, except as required by law.
We implement appropriate security measures to protect your personal information. However, no method of transmission over the Internet is 100% secure.
For questions about this Privacy Policy, please contact us at info@tacpasglobal.com.
Last updated: January 2025
By accessing and using this website, you accept and agree to be bound by these Terms and Conditions.
TACPAS Private Limited provides pharmacovigilance audit services, training programs, and recruitment solutions for the life sciences industry. Specific terms for each service are agreed upon separately.
All content on this website, including text, graphics, and logos, is the property of TACPAS Private Limited and is protected by applicable intellectual property laws.
TACPAS Private Limited shall not be liable for any indirect, incidental, or consequential damages arising from the use of our services.
For any queries, contact us at info@tacpasglobal.com.
Last updated: January 2025
Cancellation requests made more than 7 days before the program start date will receive a full refund. Requests within 7 days of the start date may be eligible for a credit transfer to a future batch.
Refund terms for audit engagements are specified in the individual service agreements signed prior to commencement of work.
Recruitment service fees are governed by the terms outlined in the individual client agreements.
For refund requests, please contact info@tacpasglobal.com.