Innovation with Integrity. Science with Impact
At Genie
Pharma, we believe the future of healthcare depends on more than science alone
— it requires vision, collaboration, and a commitment to doing what’s right.
From molecule to market, we partner with innovators worldwide to
develop, manufacture, and deliver high-quality, cost-effective active
pharmaceutical ingredients (APIs) and finished formulations.
Our
leadership team brings a combined experience of over 100 years in pharmaceutical innovation,
USFDA/EDQM-compliant manufacturing, regulatory strategy, and commercial
scale-up. Their expertise spans building greenfield manufacturing sites,
leading global R&D programs, and securing successful product launches in
over 70 countries.
With 40+
patents, 75 DMFs, and a portfolio of 340+ products, our track record speaks
for itself. But what truly sets us apart is our approach: IP-free
process innovation that enables speed to market without compromising
quality or compliance. Our facilities are strategically located in
India and marketing office in Switzerland. The facilities are
built to meet the world’s most demanding regulatory standards.
We serve as
more than just a CDMO, we’re a trusted partner who
understands the complexities of drug development, from early-stage R&D to
large-scale manufacturing. Every project we take on is guided by our
values: excellence, transparency, and a patient-first mindset.
PATENTS
GLOBAL PRESENCE
DMF
PRODUCT LIBRARY
Tailored APIs, KSMs, NCEs & CDMO projects for regulated markets
IP-free process development, impurity synthesis, analytical methods
Experienced team with strong scale-up & tech transfer skills
Full compliance with global GMP & regulatory requirements
Fast responses, proactive communication, and reliability
From gram-scale R&D to multi-ton manufacturing supply
Strict confidentiality, active client interaction, on-time delivery
High-purity products with the best impurity profile