Medical Writing KPO |
The global pharmaceutical industry is under pressure to reduce drug development cycle time and to meet increasingly tight regulatory compliance requirements in the US, Europe, and even developing markets. In addition, patents on existing drugs are nearing expiration and the new-drug pipeline is depleting. More and more companies are opting to outsource medical writing in order to tap skilled resource pools in offshore locations and obtain quality, cost-effective services.
Leveraging over 25 years of experience in the Life Sciences domain and specialized expertise in regulatory compliance consulting, Patni provides cost-efficient and high quality medical writing services to help clients reduce time-to-market for new drugs while ensuring regulatory compliance at lower costs.
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| Our comprehensive suite of medical writing services in key areas, such as pre-clinical, clinical, post-marketing, regulatory, risk management, and standard operating procedures, helps clients expedite the drug development process by ensuring that the documents for regulatory submissions are of the highest quality and comply with all applicable regulations. |
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| How Patni Can Help |
| Patni is an integrated BPO-IT services provider with demonstrated expertise in helping clients streamline operations, reduce costs, and enhance business efficiencies through global sourcing. Patni provides medical writing services to develop a wide range of documents required at different stages of the drug development life-cycle. The therapeutic areas covered include immunology, oncology, endocrine, cardiovascular, pulmonology and infectious diseases. Patni employs a proprietary toll-gate based solution delivery framework. It includes our state-of-the-art, industry-leading transition methodology that ensures the smooth transfer of medical writing processes to Patni resources. |
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