TOLMAR Facilities

• Clean room ISO 8 - ISO 5 (EU Grades A, B, C, D manufacturing environments)
• cGMP and EU cGMP compliant manufacturing
• Intrinsically safe manufacturing rooms
• Chemistry and microbiology laboratories
• Stability chambers with ICH conditions
• Multi-shift production operation
• Liquid, semi-solid and powder filling lines
• Temperature controlled warehouse storage

Inspections and Regulatory Status

• FDA and EU Approved Facility

• ISO 13485 Registered
• Regularly audited by marketing partners and various regulatory bodies