Soul Pharma Consultancy offers services in following areas

Research & Development

Formulation development of various dosage form including complex generics at client's site.
Process optimization, scale up at proposed manufacturing site.
Technology Transfer [lab to plant as well as site to site] .
Dossier review.
Guide in resolving critical regulatory queries related to product, process etc

Manufacturing & Quality

Documents preparation or review example: Master Formula Card, Master Batch Manufacturing Record, Master Packing Record, Process Validation Protocol, Process Validation Report etc.
Review of proposed CAPA
Trouble Shooting of OOT/OOS in products.
Technical support for regulatory audits.
Cost reduction by formulation reengineering, process modifications, batch size optimization, specifications revisit, alternate vendor development etc.

Other Services

Technical due diligence for acquisition.
Post acquisition portfolio management and product's transfer.