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DDReg provides regulatory services required through out the product life cycle i.e from Lab to Launch to Post Launch. Please take a closer look at the services mentioned below to get a better understanding.


Regulations related to drug & drug products continue to pose a major challenge for the global pharmaceutical and allied industry. In such situation – a sound regulatory strategy is key to th...


Any sound regulatory strategy stands on effective planning and implementation. Regulatory Operations by way of New Filings, dossier compilations or variations, running procedures on client’s beh...

Post Approval Life Cycle Management

Post approval Life Cycle Management (PLM) includes the lifecycle of a product once it has been launched in the market. It is about the maintenance of the product in the market in compliance to the reg...

Medical Writing

DDReg undertakes writing of various medical documents that form part of submission dossier, Medical content or those required for Drug Safety Management. DDReg has a team of experts who have experienc...


Every medicine is tested on a relatively small number of people before it is approved for use by the wider population, where previously undetected reactions can emerge. Each patient is a unique medici...

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