Infrastructure
World‑class, GMP‑aligned facilities designed for quality and safety.
MANUFACTURING OVERVIEW
Our facilities adhere to updated GMP norms (incl. Revised Schedule M) with stringent quality systems across every stage — raw material intake, processing, packaging, and dispatch.
Rise & Shine Pharma’s quality policy spans the full lifecycle — sourcing qualified raw materials, validated processes, and robust in‑process controls to final pack integrity. Dedicated areas, controlled environments, and validated utilities ensure consistent, reproducible outcomes batch after batch.
Key Dosage Capabilities
- Tablets (immediate & modified release)
- Hard/Soft Gelatin Capsules
- Liquid & Dry Syrups
- Ointments, Creams & External Preparations
- Eye/Ear Drops
- Powders (oral)
β‑Lactam & Cephalosporin handled in isolated, dedicated production areas.
FACILITY HIGHLIGHTS
Engineered to prevent cross‑contamination and protect product purity.
- No wood or asbestos components anywhere on site.
- Segregated zones with dedicated AHUs, de‑humidification & dust extraction.
- Color‑coded zones, areas & uniforms for absolute segregation.
- Controlled environments (temperature, humidity, filtration, particle counts).
- Unidirectional flow of men & materials for optimum productivity.
- Utilities & maintenance access from outside for safer operation.
- Ample, segregated storage with quarantine facility.
- Individual compression & coating cabins with separate AHUs.
- Dedicated β‑Lactam & Cephalosporin production suites.
- SS reverse laminar flow for dispensing operations.
- Air‑conditioned stores for raw, packing & finished goods.
- R&D center on campus for in‑house product development.
- Alternative power generation for uninterrupted production.
- 3‑micron air filtration in production departments.
- Round‑the‑clock capacity with spare bandwidth across sections.
- Third‑party & private‑label readiness for export programs.
PACKAGING EXCELLENCE
Protecting product integrity through transit, climate, and time.
Our packaging approach is built around patient safety and product stability. Materials and processes conform to international norms to ensure longevity and reliability long after leaving the production line.
- Medical‑grade, non‑toxic materials only.
- Compliance with applicable regulatory standards.
- Excellent oxygen & moisture barrier properties.
- Consistent high‑quality print & pack finishes.
- Printed shippers available on request.
Sensitive materials (e.g., aluminum/PVC foils) are stored in designated areas at controlled temperatures with access control.
Design & Clarity
Our in‑house design team ensures every pack balances clarity and contemporary styling, supporting easy identification, handling, and dispensing.
SHIPPING EXCELLENCE
Ensuring safe, climate-conscious delivery from our facility to your destination.
Our logistics protocol prioritizes product safety during transit, especially for temperature-sensitive medicines. We deploy cold chain shipping methods that maintain product integrity from dispatch to delivery.
- Ice packs are packed around the product boxes inside thick styrofoam insulation.
- Temperature-controlled interiors ensure compliance with stability guidelines.
- Shipping teams are trained in cold-chain logistics best practices.
- Tracking and handling protocols in place to reduce temperature excursions.
Our cold chain systems are ideal for heat-sensitive APIs, formulations, and R&D samples.
Validated Utilities
- Duo‑pass Reverse Osmosis (RO) / de‑mineralization water systems.
- Qualified clean air systems with monitored differential pressures.
- Calibrated, validated critical equipment with documented SOPs.
- Electronic data capture & audit trails for key processes.
Sustainability & EHS
- Zero‑discharge Effluent Treatment Plant (ETP).
- Temperature‑aware storage & cold‑chain practices where applicable.
- Periodic EHS training & drills for on‑site teams.
- Waste segregation & disposal as per regulations.
Compliance & Certifications
Our sites operate to c‑GMP and Revised Schedule M requirements with documented SOPs, training matrices, and periodic audits. Dossier support is available in CTD format, with COPPs, BE studies, and other regulatory documentation provided as per market needs.