Quotient Sciences

Clinical Trial Manufacturing

Clinical Trial Manufacturing

Understanding that early-phase clinical testing is a pivotal milestone in the development of your drug product, Quotient Sciences offers clinical trial manufacturing, testing, and certification services designed to meet your individual requirements. Our innovative method of building integrated Good Manufacturing Practice (GMP) and Good Clinical Practice (GCP) programs provides a streamlined, flexible approach to drug product supply that reflects your clinical study design and timeline. We understand the time and cost pressures you face during early-phase evaluation and work with you to ensure a rapid, seamless path from development to clinical trial supply.

We understand your need to move rapidly through clinical development and have built the capability to efficiently scale up drug product manufacturing processes to meet the demands of global clinical and patient supply requirements.

What can Quotient Sciences' clinical trial manufacturing services do for me?

• Use a variety of manufacturing approaches to make only the product you need, flexible on demand
• Tailor manufacturing, packaging, and clinical trial supplies to reflect your clinical trial design
• Improve cost efficiency by reducing drug substance and drug product waste
• Leverage our expertise in high-potency manufacturing

Dosage forms

We offer manufacturing and testing services for all major dosage forms, including:

• Solutions and suspensions
• Drug in bottle, drug in capsule
• Immediate-, sustained-, and modified-release tablets
• Solubilized formulations, including amorphous (spray-dried and hot melt extrusion [HME]) dispersions, micronized and lipidic formulations
• Gels, creams, and ointments