• Services
• Route Scouting
• Chemical Process Development
• Process Validation
• GMP Manufacture of Clinical Trial Materials
• GMP Manufacture of Commercial API’s
• Multi-Ton APIs Advanced Intermediates
• Analytical Methods Development and Validation
• Medicinal Chemistry
• Custom Synthesis
• FTE Programs

GMP Manufacture of Clinical Trial Materials

The GMP manufacturing of clinical trial material facility at Saimerak Pharma produces solid oral dosage forms, as well as semi-solid and powder sterile products containing either non-potent or potent principles.

The production of these compounds at different sizes which may range from a few units up to kilogram for solid dose, as well as semi-solids.

Our process facilities at Saimerak Pharma have been specifically designed for quick turnaround and cost-effective production.

Latest News & Events

• March 13-17, 2016 251st ACS National Meeting & Exposition, San Diego, California.
• August 21-25, 2016 252nd ACS National Meeting & Exposition, Philadelphia, Pennsylvania.
• April 2-6, 2017 253rd ACS National Meeting & Exposition, San Francisco, California.
• August 20-24, 2017 254th ACS National Meeting & Exposition, Washington, DC.