What We Do?
CRDMO Services
Vikasith delivers end-to-end CRDMO solutions — from early-stage development to commercial manufacturing. Our integrated capabilities include process development, optimization, analytical testing, and regulatory support, ensuring seamless progress through every phase of your molecule’s lifecycle.
Peptide Development
We specialize in peptide synthesis and scale-up, producing high-quality peptides from milligrams to multi-kilogram quantities using advanced sequential and segment condensation methodologies.
Generic APIs
Vikasith develops and manufactures both Prime APIs — high-volume, mature molecules — and Specialty APIs, featuring complex, niche compounds with lower competition.
Engagement Models (FTE/FFS)
Vikasith Lifesciences offers two business engagement models — Fee for Service (FFS) and Full-Time Equivalent (FTE) — providing clients with flexibility and transparency tailored to their project goals.
Core Areas of Expertise
Phase-Specific Services
Comprehensive support across every development phase, from early research to commercial scale.
Chemistry Capabilities & Technical Expertise
Strong chemistry know-how combined with advanced technical execution to solve complex challenges.
Specialty Chemicals & Agrochemicals
Expert development and supply of high-performance specialty chemicals and agrochemical solutions.
About Us
Empowering Innovation the most from Molecule to Market
Vikasith is a global leader in API contract development and manufacturing (CDMO), partnering with biotechnology and pharmaceutical companies to bring breakthrough therapies to life. We specialize in the design, development, and scalable manufacturing of complex active pharmaceutical ingredients (APIs), supporting your molecule’s journey from concept to commercialization.
Driven by Science. Defined by Quality.
With deep expertise in small molecules and peptides, Vikasith provides end-to-end solutions — from early-stage research and clinical trials to full-scale commercial production. Our advanced facilities and experienced scientific teams ensure seamless project execution with precision, reliability, and regulatory excellence.
Our Capabilities
Precision-driven capabilities supporting end-to-end pharmaceutical development and manufacturing.
Manufacturing Capabilities
Robust, scalable manufacturing infrastructure designed to meet global quality and compliance standards.
Analytical Capabilities
Advanced analytical expertise ensuring accuracy, consistency, and regulatory confidence across products.
Quality Management System
A comprehensive quality framework focused on compliance, reliability, and continuous improvement.
Project Management
Structured project execution ensuring transparency, timelines, and seamless client collaboration.
IT & Data Integrity
Secure, compliant digital systems safeguarding data integrity and regulatory readiness.
Proven Performance at a Glance
Regulatory Approvals
