ETL Healthcare - Your Trusted Partner in PV, Clinical Trials and RCM
At ETL Healthcare, we are dedicated to providing comprehensive and specialized services in pharmacovigilance, cosmetovigilance, materiovigilance, medical writing, clinical trials management, regulatory affairs, and revenue cycle management. Our focus is on ensuring the highest quality standards across all our healthcare solutions.
Learn more about our commitment to quality, compliance, and innovation in the healthcare industry.
Meet our CEO
Liana Kasyan, MD, MPH
- Founder/CEO at ETL Healthcare
- Member of the WHO Global Patient Safety Network (GPSN)
- Technical Advisory Board Member at Ancillarie
- Member of the International Society of Pharmacovigilance (ISoP)
- Global Pharmacovigilance Society Ambassador for Armenia
- International Editorial Board Member for the Journal of Pharmacovigilance and Drug Research (JPADR)
- Board Member of the Armenian Association of Specialists in Evidence-Based Medicine (AASEBM)
- Co-founder of “Do not Harm’’ Health NGO
Meet our Senior Advisor
Dennis J. Van Liew, Jr.
Denny Van Liew is a senior advisor to ETL Healthcare, bringing extensive expertise in pharmacovigilance, regulatory operations, and healthcare strategy. He has held leadership positions at Pfizer, Bioclinica (now Qinesca),
Kinapse (now Syneos Health), and Red
Nucleus, where he led significant transformation initiatives integrating regulatory and safety organizations for global pharmaceutical clients.
At Red Nucleus, Dennis specialized in modernizing operating models and improving process performance across R&D, Regulatory,
and PV functions. As founder of The Pareto Group, he advises healthcare and precision medicine ventures on scaling operations, governance, and strategic partnerships.
Dennis serves on the board of AntaresGenomics and as Treasurer of the International Society of Pharmacovigilance (ISOP) North America chapter. His extensive industry experience enables ETL Healthcare to enhance its capabilities in drug safety, regulatory compliance, and operational excellence.
Meet our Partners
Priyanka Dhar Trikha
Priyanka Dhar Trikha, a seasoned professional in the field of Pharmacovigilance and Drug Safety, with over 15 years of international experience spanning India, the United Kingdom, Switzerland, and now Vietnam.
With a background in Biotechnology Engineering and a Master’s degree in International Business, I’ve built a career at the intersection of science, global regulatory requirements, and operational excellence. I began my journey at a Clinical Research Organization (CRO) in India, which laid the foundation for a global career. From there, I moved on to leadership roles with CROs in the United Kingdom and Switzerland, gaining hands-on experience in managing clinical trial safety, post-marketing surveillance, and ensuring regulatory compliance across multiple regions and therapy areas.
My expertise includes comprehensive case processing activities, oversight of Local Qualified Person for Pharmacovigilance (QPPV) services, and deep proficiency in safety databases—especially Oracle Argus. I've successfully led initiatives to establish electronic gateway connections with global regulatory authorities and supported database configurations to meet the specific needs of pharmaceutical clients.
Currently based in Ho Chi Minh City, Vietnam, I support organizations across the APAC region, helping them strengthen their pharmacovigilance operations, navigate audits and inspections, and build compliant safety systems. I’ve had the privilege of training and mentoring diverse global teams across Europe, India, and the US, with therapeutic area expertise in oncology, respiratory diseases, liver conditions, viral infections, ophthalmology, and more.
Shweta Anand
Dr. Shweta Anand, a seasoned Healthcare consultant and Pharmacovigilance professional with over 10 years of international experience across Asia, Europe, and the Middle East. Holding a Bachelor’s in Dental Surgery from India and a Master of Public Health from the University of Hong Kong. I bring a multidisciplinary approach that combines clinical insights, regulatory expertise, and strategic foresight to advance patient safety and drive commercial growth in the pharmaceutical, biotech, and medical device sectors.
I bring expertise across pre and post-marketing settings, spanning diverse therapeutic areas and medical devices. I have led global safety operations, with proven strengths in ICSR management, signal detection, benefit-risk assessment, and regulatory submissions. My work with real-world evidence and big data has resulted in seven peer-reviewed publications, advancing the science of medication safety.
As a Local QPPV in Hong Kong, I have managed pharmacovigilance activities and served as the key liaison with the local health authority, ensuring full compliance with adverse event reporting timelines, risk management protocols, and data privacy standards.
Based in Dubai, I partner with pharmaceutical and healthcare organizations to optimize pharmacovigilance operations, ensure compliance with global regulatory standards, and drive business development across international markets. My work bridges drug safety with broader commercial objectives, underpinned by a strong commitment to scientific integrity and strategic impact.
Amiit Keshav Naik
Clinical Research Professional and his experience includes setting up Data Management & Biostatistics departments with managing team size of 250 professionals for various multinational CROs.
With more than 22 years of professional experience including 17 years of Professional Experience for top CROs; He has proven his strengths in Project Management which comprise of monitoring processes like Data Management, IVRS, SAS programming processes and External Vendors for more than 200 studies across different therapeutic areas.
He has provided his expertise to the Business Development team to develop proposals for Bid Defence Meetings. His strong leadership and communication skills facilitates diverse cross-functional teams to deliver positive results.
He has built reputation for efficiently meeting challenges in rapidly changing environments while consistently delivering excellence.
Amiit also has supported academia as visiting faculty for Data Management subject at a Pharmacy College. He has also worked as paper setter and examiner for Biostatistics and Data Management subjects for M.Sc. Pharmaceutical Medicine.
He has built reputation for efficiently meeting challenges in rapidly changing environments while consistently delivering excellence.
Amiit also has supported academia as visiting faculty for Data Management subject at a Pharmacy College. He has also worked as paper setter and examiner for Biostatistics and Data Management subjects for M.Sc. Pharmaceutical Medicine.