Clinical Trial Materials Formulation
Chemvent specializes in the custom formulation of phase I and phase II clinical trial materials.
Our state-of-the-art laboratory is FDA-registered and DEA-Licensed. Clinical trial material development projects are performed according to strict current Good Manufacturing Protocols (cGMP).
Our lab accreditations qualify Chemvent to expertly manage CTM projects with challenges including controlled materials requirements.
In the pre-formulation design phase, you will meet with the Chemvent CTM experts to discuss your project needs. From consultation through formulation, we will manufacture your product according to your custom specifications.
Our CTM manufacturing capability includes:
- Oral solutions
- Oral suspensions
- Othalmic drops
- Nasal preparations
Once we have successfully formulated the clinical trial materials to your satisfaction, we are able to offer services that include rigorous packaging and release testing. This will ensure that your product is safe and effective for standard use.
Chemvent is also able to assist with clinical trial supply packaging and labelling development. We are partnered with seasoned experts in the CTM manufacturing industry who offer manufacturing services to clients who are increasing scale.
With Chemvent’s support and development services, your product will be efficiently and expertly formulated for success in the phases of clinical trials.
All projects performed by Chemvent are kept under strict confidentiality, as agreed to within our Non-Disclosure Agreement. All clinical trial materials developed within Chemvent belong to the sole property of the respective contractor.