Luhan Pharmachem Co., Ltd.

A.Quality and regulations consulting services:

(1) We have our own strict quality evaluation system.All assessment report, all products of export orders according to the strict assurance procedures for quality evaluation, ensure in each link bulletproof, has the specialty the QA and QC departments engaged in raw material quality control, production quality control, product quality control, perfect quality analysis of control, because we have strict quality control system, we can have conditions to help domestic manufacturers to provide regulations, quality control system certificate for foreign markets, such as the United States market, according to the GMP medicines (21 cfr211) standards and customer requirements to carry out the pre-qualification and put forward revision plans and make it conform to GMP requirements in the United States;The European market, according to the latest eu GMP and customer requirements to carry out the trial version of pharmaceutical preparations put forward revision plans and make it accord with the eu GMP requirements;Other markets: in accordance with the pharmaceutical administration law of the People's Republic of China, the implementation regulations destination market drug GMP standard or WHO GMP standards related to pharmaceutical preparations enterprises operating and processing and modification of files.Such as India, Brazil, Argentina, Japan and other countries.Help domestic manufacturer to the international market;We can help enterprises to complete the commercial production of API.Will its brand development for the world brand.

(2) Inspection service: for some inspection system is not perfect production enterprises, we have the ability to help the enterprises to carry out drug related inspection, we also cooperate with the third party inspection institutions closely, we can provide customers advanced technology, in accordance with related regulations and inspection results reliable third party inspection report.