Our journey
Manufacturing
Ecosystem
A Licensed, WHO-GMP Aligned Production Framework Supporting Global Healthcare.
Aidotick Pharmaceuticals operates through a licensed manufacturing ecosystem that combines the capabilities of advanced WHO-GMP compliant facilities with our internal oversight, regulatory governance, and stringent quality protocols.
Our manufacturing model is designed to ensure pharmaceutical excellence without claiming facility ownership, reflecting a diplomatically positioned, internationally aligned corporate identity.
This ecosystem allows Aidotick to deliver products that uphold the highest standards of:
- Safety
- Efficacy
- Stability
- Regulatory compliance
- Global documentation integrity
Every batch produced under our license represents our commitment to consistent quality and global healthcare responsibility.
A Multi-Facility Ecosystem Designed for Precision
Aidotick works within a licensed production environment supported by multiple WHO-GMP aligned facilities across India.
This diversified network allows us to ensure:
- High production capacity
- Wide therapeutic coverage
- Flexible timelines
- Risk-mitigated supply reliability
- Scale-up capability for global demand
Our strategic partnerships with manufacturing facilities enable us to produce:
- Tablets
- Capsules
- Oral liquids & suspensions
- Injectables (liquid & dry powder)
- Ointments, creams & gels
- Nutraceutical formulations
Each facility operates under validated processes, documented protocols, and full regulatory oversight.
Our Manufacturing Governance Model
Aidotick maintains direct oversight of the manufacturing lifecycle through:
1. Process Documentation & Specification Control
We ensure every formulation is manufactured strictly according to:
- Approved master batch records
- Standard operating procedures
- Validated manufacturing processes
- International pharmacopoeial standards
2. Quality Assurance Leadership
Our QA team governs:
- Material qualification
- In-process controls
- Finished product release
- Documentation verification
- Deviation & CAPA systems
3. Regulatory Alignment
All outputs adhere to global registration requirements, including:
- CTD
- ACTD
- MOH-specific dossier formats
4. Transparency & Audit Readiness
Our facilities maintain full audit readiness for:
- Ministry of Health teams
- Partner audits
- International regulatory inspections
Advanced Infrastructure Highlights
Although Aidotick does not claim facility ownership, we ensure that our licensed ecosystem meets global benchmarks across:
Environmental Controls
- Classified cleanrooms
- HEPA filtration systems
- Temperature & humidity-controlled zones
- Automated air monitoring systems
Utilities & Safety Systems
- Purified water generation (RO/DM)
- HVAC-driven climate stability
- Effluent treatment plants
- Fire and occupational safety systems
Production Equipment
- High-speed compression machines
- Capsule filling systems
- Automatic liquid filling lines
- Injectable vial filling & sealing lines
- Blister & carton packaging equipment
Documentation & Traceability
Aidotick ensures end-to-end traceability through:
- Batch Manufacturing Records (BMR)
- Batch Packaging Records (BPR)
- Cleaning validation reports
- Calibration logs
- Material movement registers
- Stability study documentation
Documentation integrity is at the core of our manufacturing philosophy, ensuring regulatory trust across global markets.
Built for Global Supply Chains
Our ecosystem is optimized for:
- International distribution
- Region-specific packaging needs
- Temperature-sensitive logistics
- Multi-country regulatory submissions
- Market-specific batch customization
This ensures reliable supply for:
- Distributors
- Government tenders
- Pharmacy chains
- Humanitarian organizations
- Private label partners
Closing Statement
Aidotick’s manufacturing ecosystem reflects a modern pharmaceutical model — advanced, compliant, transparent, and globally dependable.
It enables us to deliver trusted medicines for global healthcare systems while maintaining a corporate identity built on scientific and regulatory excellence.