Sourcing Evaluation

At Rushi Pharma, sourcing is not transactional — it is systematic

Manufacturing Site Verification:

• Physical verification of manufacturing facility and coordinates
• Assessment of installed production capacity
• Capacity utilization analysis
• Infrastructure and scale validation

Regulatory & Compliance Review:

• Verification of cGMP systems
• Review of manufacturing licenses and certifications
• Audit history assessment (client / regulatory agency audits)
• Regulatory documentation status

Product Assessment:

• Manufacturing status (regular / campaign / made-to-order)
• In-house specifications and Method of Analysis (MOA)
• Historical price trend evaluation (6–12 months)
• Commercial sustainability analysis

Quality & Technical Validation:

• Technical documentation review
• Pre-shipment samples
• Third-party analysis (if required)
• Ongoing technical coordination