专业的医药研发团队，一流的设备设施，让汉维成为国内第一个按照EU GLP 标准建立和运行的宠物药品研发实验室。多项新药证书、多项制剂专利授权是汉维领先、专业的宠物药品研发实力的佐证。
The professional R&D team, and the state-of-the-art facility, make Hanvet to be the first veterinary formulation development laboratory in China according to EU GLP guideline.So far Hanvet has been granted many New Drug Certificates and authorized Patents.
Hanvet R&D activity includes:
Full range of service modules aiming to provide "one-stop shop" formulation services to meet customers' development needs at various stages.
o Physical pharmacy profiles: solubility and viscosity in lipids, surfactants/polymers, partition coefficient (logP, logD), solid state characterization, pH, solid state stability, solution stability;
o Polymorph screening;
o Salt form selection;
o Powder characterization: particle size evaluation and specification recommendation;
o Drug excipients compatibility;
o Formulation pre-designing;
o Formulation screening using stress study and stability study;
o Process selection based on physicochemical and physical properties of the drug candidate;
o Containers, storage and shipping conditions for development candidates;
o Tech transfer of formulation and manufacturing process to clinical supply manufacturing sites;
o Develop and validate analytical testing method, assay and impurity;
o Establish product specifications based on pre-formulation and formulation data;
o Support stability testing of prototype formulation;
o Provide forced degradation profiles and elucidate degradation pathway and possible degraded products;
o GMP guided analytical development activities.