The Minds Shaping Global Healthcare at Medylife
Mr. Bishnu Rijal
Mr. Bishnu Rijal serves as the Director of Medylife Global FZE, a Dubai-based pharmaceutical company specializing in the international trade of Active Pharmaceutical Ingredients (APIs), intermediates, and finished dosage formulations. With a strong foothold in global sourcing and pharmaceutical logistics, he plays a pivotal role in steering the company’s vision toward reliable, ethical, and innovative healthcare solutions.
With over a decade of experience in the pharmaceutical and healthcare sector, Mr. Rijal has successfully led strategic expansions into emerging markets across the Middle East, Africa, and South Asia. His leadership is defined by a deep understanding of regulatory frameworks, market dynamics, and client partnership development.
Key Expertise:
Global Pharmaceutical Trading & Distribution
API & Formulation Sourcing
Regulatory Affairs & Market Compliance
Strategic Procurement & Vendor Alliances
Supply Chain & Export Operations
Vision:
To position Medylife Global FZE as a trusted global partner in pharmaceutical trade, committed to improving access to affordable and high-quality medical products across developing and regulated markets.
Quote:
“In today’s world, access to quality medicine is not just a necessity — it’s a right. At Medylife Global FZE, we are committed to bridging that gap through trusted partnerships, uncompromised standards, and a relentless focus on global health impact.”
— Bishnu Rijal, Director, Medylife Global FZE
Mr. Khalid Al Mansoori
Mr. Khalid Al Mansoori is a seasoned pharmaceutical executive with over 16 years of experience in regulatory compliance, government liaison, and policy advocacy within the healthcare and life sciences sector. At Medylife Global FZE, he leads all initiatives related to regulatory frameworks, product registrations, and strategic engagement with health authorities across the GCC and MENA region.
Khalid is highly respected for his ability to navigate complex regulatory environments, ensuring that Medylife remains fully aligned with evolving industry standards and government expectations. His contributions have significantly accelerated the company’s market approvals and institutional partnerships across the region.
Expertise:
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GCC & MENA Regulatory Affairs
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MOH, SFDA, and DHA Liaison
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Pharma Licensing & Compliance Strategy
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Healthcare Policy & Risk Advisory
Education:
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B.Sc. in Pharmacy – Gulf Medical University, UAE
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Executive Diploma in Public Health Policy – London School of Hygiene & Tropical Medicine
Quote:
“Compliance is not a barrier to growth—it is the foundation of trust.”
Ms. Nivedita Arora
Ms. Nivedita Arora brings over 14 years of experience in pharmaceutical supply chain management and regulatory affairs. As Director of Global Supply Chain & Regulatory Affairs at Medylife Global FZE, she oversees the seamless coordination of international logistics, compliance frameworks, and quality systems across the company’s operations in more than 25 countries.
Her ability to align complex regulatory requirements with efficient supply chain strategies has been critical in expanding Medylife’s footprint across the GCC, Africa, and Southeast Asia. Nivedita is known for her precision, risk management acumen, and hands-on approach in driving operational excellence.
Expertise:
Regulatory Strategy (GCC, WHO PQ, EU Standards)
Pharma Supply Chain Optimization
GMP/GDP Compliance & Audits
Risk-Based Inventory & Logistics Management
Education:
M.Pharm – Delhi Institute of Pharmaceutical Sciences & Research
Certification in Supply Chain Excellence – MITx, USA
Quote:
“In pharma logistics, precision isn’t a goal—it’s a mandate.”