ProRelix Research's Regulatory Affairs services in USA, India, Europe & Australia provide expert IND, CTA, NDA, ANDA, eCTD services for Clinical Trials, We provide expert support in regulatory affairs. Our drug development programs include regulatory support of clinical trials, new chemical entity’s development (NCE), marketing products, generics, and medical devices in India, USA, Europe, and UK as well. Kindly visit our website www.prorelixresearch.com.