Our R&D scientists are multidisciplinary with backgrounds in pharmaceutics, pharmaceutical analysis, and pharmaceutical chemistry. They are well-trained and have decades of experience in pharmaceutical industries working in FDA and DEA regulated environments. Their expertise can be found in novel dosage form design and development as well as analytical method development and validation.
As an organization that prides itself on its technological and human resources, we strive to build a team that incorporates the following the core values.
Teamwork: Honest communication and cooperation.
Passion: Focus and drive for our work.
Excellence: Responsibility and commitment to be the best.
We work as one team to win as one team.
RESEARCH & DEVELOPMENT
Humanwell’s scientific expertise covers a wide variety of products, offering high-class pharmaceutical development services. Our scientists, who have decades of experience, will provide customized solutions to meet your developmental needs.
DEA Manufacturer License for Schedule II-V
DEA Analytical License for Schedule I-V
General Physical and Chemical Characterization
Oral Solid Dosage Formulation and Process Development
Immediate Release, Modified Release (ER, SR and CR)
Complex Injectable Formulation and Process Development
Liposomal Formulation, Emulsions
Analytical Method Development and Validation
Compendial Method Verification
ICH Stability Chambers
25°C/60%RH; 30°C/65%RH; 40°C/75%RH and 5 ± 3°C