The tormenting desire to serve mankind and also the ambition to make a dent in one of the fastest growing Pharma industries is the name ZOTA HEALTH CARE LTD. Now ZOTA is turned into a GROUP with 22 Division in its fold, viz.
To meet the demand of the trade, ZOTA Group can today boldly claim to have over Two thousand eight hundred products in its mix. To free the doctors from the dependence on multiple of companies, ZOTA today offers an unmatched range of products under a single roof. The strength of the natural treatment too has been promoted with separate AYURVEDIC Division.
ZOTA formed the required traits of a truly STANDARD Pharma Organization with the ETHICS of not indulging into unscrupulous practice and unwavering QUALITY with ZERO DEFECT; in fact, ZOTA was approved with the prestigious ISO 9001:2008 Certification & CRISIL SE 1A. This Rating Indicates "HIGHEST" Performance Capability and "HIGH" Financial Strength. In addition to Quality Control, the company has adopted Total Quality Management System, which leaves no stone unturned to keep the product with International Quality Standards.
Our R&D is extensively working on unique and novel formulations especially in nutraceuticals. Already applied 16 unique different formulations for patent and amongs them 7 products is applied for PCT for 142 countries. The formulation which has gone for PCT already introduced in domestic market and accepted by medical fraternity very well. RTFit is a unique and novel combination of two amino acids for liver disorders especially for alcoholic hepatitis with unique mode of action without any complication due to its natural origin. Apart from RTFit other patent applied formulations will be available shortly. Company has already started the clinical trial of RTFit in various liver disorders with good no. of patients to evaluate the efficacy and safety of RTFit.
ZOTA has setup the production facility for the EXPORT at Surat in the Surat Special Economic Zone, Nr. Sachin Railway Station, Sachin, Surat. (Gujarat). This manufacturing plant follows cGMP & WHO conditions comparable with the international regulations (MCC South Africa & MHRA U.K And USFDA.). The company is primarily involved in manufacturing of Tablets & Capsules (General group).
QA CHEMIST 1. Preparation, review, distribution, Retrieval and Destruction of all Standard Operating Procedure (SOPs) or any master document in Production, Quality Control, Engineering, Quality Assurance, Store and Personnel & Administration & IT. 2. Identification and control of changes & Deviation through Change Control Form (CCF) & Deviation form respectively applicable to various functions of the plant that affects ...