Your regulatory gateway
into Thailand
Molecular Pharming Solution offers full-service CDMO & CRO quality excellence solutions — serving partners across pharma, biotech, and diagnostics.
Regulatory Services
- Drugs, Medical Devices, Cosmetics Registration
- GMP Facility Licensing Facility certification
- GMP Clearance
Document Preparation
- Dossier/Document Preparation and Review
- Tailor-made IND and IDE submission for clinical trial approval
- CTD, ACTD, and CSDT for product licensing
Compliance & Quality Planning
- Quality Target Product Profile (QTPP): Definiting product specifications
- Gap Evaluation and Feasibility Assessment
- Strategic Regulatory Planning
Protocol Design & Development
- Protocol design and development
- Clinical trial document development
- IRB package preparation and submission
Synergistic Science Solutions
- Product efficacy testing
- User experience testing
- Scientific study design crafting consultant