Manufacturing & Testing
Manufacturing & Testing
Contract Manufacturing
At QCS, our team has extensive experience and expertise in drug development, manufacturing and primary packaging. We understand the critical role these processes play in ensuring the quality and safety of clinical trial supplies.
Services
Collaboration with Approved Contract Manufacturing Organizations (CMOs):
- We work closely with our approved CMOs to develop and package the required dosage forms.
- Our contractors hold MHRA licenses, ensuring compliance with regulatory standards.
Tailored Solutions:
- Whether it’s formulation development, manufacturing, or primary packaging, we customize our services to meet your specific needs.
Analytical Services
Our analytical services team specializes in supporting clinical trials throughout their lifecycle. We focus on development, validation, release and stability testing.
Offerings
Full Specification Testing:
- We collaborate with approved contract laboratories to conduct comprehensive specification testing for clinical trial materials.
Importation Testing:
- Rigorous testing ensures compliance upon importation.
Long-Term Stability Assessment:
- We set up stability studies to monitor the integrity of clinical supplies over time.
For all your clinical trial supply requirements, please feel free to contact our dedicated team today. We’re here to assist you in delivering successful trials. 🌟