 product claims, active marker (or indicator) confirmation; analytical method scouting/development/validation/transfer, prototype stability testing and evaluation; specification of new raw materials and final product; testing for prototype and final registration sample; competitive product analysis;  analytical method establishment for current products in case of quality issue

 setting the specification for the raw material/excipient, in-process and finished product; quality Control and release for raw material/excipient, in-process and finished product; stability testing; process change control and validation; evaluation of production deviation and decision making;  change control on supplier; new supplier qualification;; supplier audit; manufacturing process related validation on new product

 On-site audit, enterprise specification check, testing for the new registered drug/healthy food provided by the enterprise; Specification drafting or review on imported raw material; Specification drafting or review on ChP, GB, industry standard, regional standard; Inspection and evaluation for the drug product in the market; GMP audit to the pharmaceutical manufacturing enterprise;

Preparation of internal product including oral liquid, capsule, injection, etc;Quality control for the raw material, in-process and finished product