Drug Product Manufacturing Excellence
Trusted CMO partner delivering end-to-end pharmaceutical manufacturing solutions with commercial-scale capabilities, regulatory compliance, and supply chain integration.
15B+
Tablets per year
120M+
Capsules annually
8
FDF facilities
Our Comprehensive Services
cGMP Manufacturing
State-of-the-art facilities providing end-to-end production of finished drug products that meet global regulatory standards.
Eight fully integrated FDF facilities across Hyderabad campus
Dedicated sterile and non-sterile suites with controlled cleanroom environments
Specialized infrastructure for HPAPIs, hormone, cytotoxic, and biologic formulations
Automated filling and packaging lines with modular design
Annual capacity: 15B tablets, 120M capsules, 8M sachets
4M parenterals (liquid & lyophilized), 40M oral suspensions
Final Deliverables:
Fully manufactured, regulatory-compliant commercial drug products
Complete GMP batch records and QC release certificates
Documentation ready for regulatory inspection
OnTime Delivery
Predictable delivery of materials, milestones, and regulatory documentation through robust project management processes.
Dedicated project managers per client with cross-functional team support
Robust production planning and inventory management systems
Multiple manufacturing lines and backup suites to prevent delays
Proven reliability delivering >95% of batches on schedule
Real-time tracking and milestone monitoring
>95%
Of batches delivered on schedule
Final Deliverables:
Dedicated project managers per client with cross-functional team support
On-time batch release and shipping aligned with program timelines
Lifecycle Management
Strategic lifecycle support to maximize long-term value and compliance as products evolve post-launch.
Transfer Process
Reformulation services for extended-release, pediatric dosage, taste-masking
Pack redesign, secondary packaging updates, and serialization
Global labeling compliance (US FDA, EU FMD, India DAVA)
Post-approval change management and site transfers
Stability bridging and comparability protocols
Continuous quality improvement and CAPA execution
Final Deliverables:
Lifecycle enhancement batches and reformulation variants
Regulatory variation dossiers and stability bridging data
Updated labels, packaging designs, and serialization files
Ready to Partner with CRAMSN?
Let's discuss how our comprehensive CMO services can support your drug product manufacturing needs from clinical to commercial scale.
