Our Services

We manufacture and supply world class formulations, existing as well as custom branded ones as per your requirements globally. Our manufacturing facilities are based in India. These state of the art manufacturing units are WHO – GMP certified, as well as approved by the various regulatory bodies where we trade and supply our formulations.
Our existing manufacturing facilities are based out of Chennai, Tamilnadu State ( South India ) and Mehsana and Bhilad, Gujarat State ( West India )
As a overall company policy we adhere to TQMS. ( Total Quality Management System ) where you can be assured of end to end management from our end. Starting from manufacture to dispatch and receipt at your premises.
We ensure Economy with Global Quality, Efficacy, Safety and Reliability of our products.

We operate and manage a Global Supply Chain for our partners with flexibility, responsiveness and reliability.
All shipments are individually monitored from our office from departure to delivery at final destination. The transport solutions are partnered with professionals from the industry who ensure high quality standards and provide end to end logistics solutions such as shipping, clearing and forwarding.
Sante Plus is committed to GDP in its distribution model and we thoroughly practice globally regulated supply chain standards including

• Consignment monitoring
• Controlled ambience transit < 25°C
• Private label packing and labelling under secure conditions
• Proper storage of goods in the warehouse at our end.

Today’s global competition demands faster turnaround cycles, from product development to market access. Regulatory affairs play an important role in coordinating scientific endeavors with regulatory demands throughout the life of the product to ensure fast turnaround in business.
Medical services functions hands in hand with regulatory affairs to ensure every product file is adequate and accurate in its data submission to the regulatory authorities.
We create and manage the following activities globally for our partners.

• Regulatory track of ever changing legislation all across operational parameters
• Compilation of dossiers as per latest guidelines given by each country. CTD / Country Specific
• Bio availability & bio equivalence studies
• Drug Master file ( DMF ) preparation for open and closed parts
• Medical writing through registration activities

Partnerships: We forge reliable and trustworthy partnerships globally for the following activities:

• Contract Manufacturing
• Co – Marketing
• Licensing
• Agency & Distributor level marketing agreements.

Trade: We enable local businesses as well as local agents with the manufacture and supply of branded generic formulations. These can be supplied under our own trade mark or any other approved customized trademark to suit local conditions and market characteristics.
We also provide all marketing and branding support to set up and grow the market to gain incremental accessibility and reach (Medico Marketing)