Innovation
CPL-Pharma: Unlock your potential
We accelerate the journey from molecule to market by delivering end-to-end CDMO solutions, ensuring faster, safer, and smarter access to life-changing therapies worldwide.
Years of Excellence
Global Clients
Countries Served
Who We Are
About Us
At the forefront of pharmaceutical innovation, CPL Pharma stands as a trusted API CDMO partner, committed to helping global healthcare companies bring life-saving therapies to patients faster, safer, and smarter. Our science-led approach enables us to drive innovation from discovery to delivery, ensuring seamless support across every stage of drug development and manufacturing.
With strong regulatory expertise, state-of-the-art facilities, and a collaborative mindset, we go beyond manufacturing—we co-create success with our partners. By combining advanced technologies, sustainable practices, and a customer-first approach, we deliver reliable, high-quality solutions that empower growth and transform healthcare outcomes worldwide.
Vision
To be recognized as a global leader in API and CDMO services, delivering breakthrough healthcare solutions through science, innovation, and operational excellence.
Values
We are driven by Integrity, Innovation, Sustainability, and Customer-Centric Collaboration—principles that guide our every decision and partnership.
Promise
With global delivery capabilities and a collaborative mindset, we ensure long-term partnerships built on trust, innovation, and a shared commitment to success.
What We Do
Our Services – API & CDMO Offering
End-to-End Development
Seamless support from preclinical research to full-scale commercialization.
Innovative Manufacturing
Advanced technologies for APIs, biologics, and complex generics.
Regulatory Expertise
Strict compliance with USFDA, EMA, WHO, MHRA, PMDA, and more.
Scalable Solutions
Digitally integrated Industry 4.0 facilities with AI-enabled systems.
Facilities
Our World-Class Facilities
Dahej Facility
Greenfield, state-of-the-art DCS-controlled API manufacturing unit ensuring purity, consistency, and sustainability.
Ankleshwar 1 & 2
Accredited by USFDA, PMDA Japan, EDQM Europe, WHO Geneva, ANVISA Brazil.
R&D Facility
Located at CSBU R&D (2nd floor), with 150+ scientists and advanced labs in synthetic chemistry, analytical studies, and process engineering.
Leadership Team
The Leaders Behind Innovation
Our executive team brings decades of scientific, operational, and strategic expertise to drive CPL Pharma’s
Biswajit Mitra
Mr Mitul Dave
Vikas Vij
Process
Cadila’s CDMO Project Management process
Project Alignment
Coordinating multiple CDMO projects (e.g., Research, Process development, Analytical method validation, Scale-up) to ensure alignment with drug (Substance & Product) development strategy and timelines.
Regulatory Compliance
Maintaining adherence to all relevant regulatory guidelines (USFDA, EMA, EDQM, ICH) throughout the drug development process, including documentation and quality control procedures.
Risk Management
Identifying potential risks associated with manufacturing processes, raw materials, and analytical methods, and implementing mitigation strategies to minimize their impact.
Resource Management
Effectively allocating personnel, equipment, and budget across different CDMO projects to optimize efficiency, Cost effectiveness and meet deadlines.
Quality Assurance
Implementing robust quality systems to ensure the consistent production of high-quality drug Substance and products, including thorough validation and quality control procedures
Developing program plans
Creating a comprehensive program roadmap outlining key milestones, timelines, deliverables, and resource requirements for each CDMO project.
Stakeholder management
Communicating effectively with cross-functional teams (R&D, regulatory affairs, quality assurance) to ensure alignment and address potential issues.
Progress monitoring
Tracking project progress against the program plan, identifying potential delays, and taking corrective actions as needed.
Change management
Managing changes to the program scope or requirements, ensuring proper documentation and communication with all stakeholders
Reporting & analysis:
Providing regular updates on program status, key metrics, and performance indicators to senior management.
Research & Development
Driving Science, Delivering Solutions
Our R&D is powered by more than 150 scientists with expertise in:
- Robust, scalable & green chemistry-driven API process development.
- Advanced analytical tools: XRD, GC-MS, LC-MS, NMR, HPLC, DSC, TGA & more.
- Engineering studies: Thermodynamics, Process Safety, Crystallization, Drying & Flow Engineering.
- Quality by Design (QbD), Process Analytical Technology (PAT), and DOE studies for optimized results.
Engineering
Manufacturing Technologies
State-of-the-art Technology from Glatt for Granulation, Coating and ACG for Capsule filling provides consistent quality and high through put
Manufacturing Equipment & Capacity (Gujarat)
Our Gujarat facility is designed to meet global regulatory standards, delivering consistent quality and efficiency across production lines. With advanced automation, it handles large-scale output while staying flexible for multiple dosage forms, supported by strict quality assurance.
The plant also emphasizes sustainability, innovation, and strong R&D support. Backed by modern infrastructure and skilled teams, we adapt quickly to market needs, making us a trusted partner for both domestic and international markets.
| Manufacturing Capacity (Oral Solid Dosage) |
Manufacturing Capacity (Injectable) |
||||||||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
||||||||||||||||||||||||||||||||||||||||||||
Sustainable Future
Sustainability & ESG Commitment
Sustainability is core to CPL Pharma’s operations. From eco-conscious manufacturing to energy-efficient R&D practices, our ESG commitment ensures we contribute positively to society, healthcare, and the environment.
Standards
Regulatory Accreditations
Contact Us
Let’s Partner for Innovation
Whether you are looking for end-to-end API development, CDMO services, or research collaboration—our team is here to help.