Elevating Research Empowering Discovery.
We are a trusted Contract Research and Manufacturing Organization specializing in API Intermediates, process development, and scalable pharmaceutical innovation. From concept to commercialization, we transform chemical complexity into clinical-ready success.
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Innovation in Action
Watch how CiVentiChem redefines scientific excellence through collaboration, precision, and technology.
30
Years of
expericence
About CiVentiChem
Founded in 1994, CiVentiChem is a leading Contract Research and Manufacturing Organization (CRMO) offering specialized services in API Intermediate development, medicinal chemistry, and custom synthesis.
- With 30+ years of experience, we help global pharmaceutical and biotech partners accelerate discovery through innovation and compliance.
- Our mission is to bridge scientific creativity and industrial scalability with integrity, speed, and precision.
Years of Expertise
IP Protection
Scalable Solutions
Syncstream
Services We Provide
Building the Foundation for Future Therapies
We ensure every research program delivers meaningful results. Our medicinal chemistry division focuses on designing and optimizing molecules that form the foundation of new API Intermediates.
- Smart molecular design and SAR optimization
- Advanced analytical monitoring and reaction control
- Full compliance with regulatory and environmental standards
From Bench to Bulk with Precision
We transform lab-scale discoveries into commercially viable processes. Our process development experts focus on scalable synthesis and cost-efficient routes for producing high-quality API Intermediates.
- Route scouting and optimization for yield improvement
- Sustainable, reproducible scale-up solutions
- Adherence to GMP and EHS standards
Tailored Chemistry for Complex Challenges
Every molecule tells a story — and we make sure yours is told with accuracy. CiVentiChem delivers custom synthesis of complex intermediates, impurities, and reference standards, ensuring reliability and confidentiality.
- Multi-step, chiral, and heterocyclic synthesis expertise
- Strict IP protection and complete documentation
- Rapid turnaround with scalable flexibility
Where Innovation Scales to Reality
From pilot to production, our GMP-compliant facilities are engineered to handle precision manufacturing of API Intermediates and fine chemicals with consistency and control.
- End-to-end production traceability
- Validated processes aligned with FDA & EMA norms
- Comprehensive quality checks at every stage
Assuring Quality from Molecule to Market
Our analytical division supports every phase of your API Intermediate journey — from method validation to final submission.
- Analytical method development & impurity profiling
- Regulatory documentation for FDA, ICH, and EMA compliance
- Stability testing & data integrity assurance
Our Proven Scientific Workflow
01
Step
Discovery & Feasibility Assessment
02
Step
Development & Optimization
03
Step
Scale-Up & Validation
Our Expert Scientists
Dr. Bhaskar Venepalli
Co-Founder & CEO
Dr. Srinivas (Vasu) Chittineni
Co-Founder & Managing DirectorLove from Clients
“CiVentiChem delivers exceptional reliability and scientific depth. Their API Intermediate development services exceeded expectations.”
VP
VP, Process R&D (USA)“A trusted CRMO partner for over a decade — their technical insight and scalability helped us accelerate to commercial success.”
Director
Director, Pharmaceutical Operations (Europe)Latest Media Update
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