WHO-GMP Certified- 3/2016
Indore INDIA

72/5, Muradpura (Orangpura) Indore


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Regulatory Accrediations

Our expertise in understanding and complying with the regulatory frame works of various countries has resulted in a successful track record of timely and extensive approvals. Our regulatory affairs team is capable in preparing and submitting dossiers as per the CTD/ ACTD guidelines and efficient in giving response to the queries.We are committed to providing a quality product while meeting the regulatory compliance.

At Zenith, we are committed to develop world class medicines to benefit the patients at affordable prices.Our R & D personnel are focusing on certain niche therapeutic segment for which developmental work is going on. In coming time we shall introduce some new formulations to the market for specific therapeutic segment.

We have highly qualified staff & an ultra modern well equipped product development lab .