ProRelix Research’s Regulatory Affairs services provide expert support in drug development programs. This is including regulatory support of Clinical Trials, New Chemical Entity’s development (NCE), Marketing products, Generics and Medical devices.
Finished Formulations:
Clinical Trial Application:
Active Pharmaceutical Ingredients:
Compilation and filing of DMFs, ASMFs and CEP’s / COS.
List of Services:
Our Pharma Regulatory Affairs services provide expert support in drug development programs. This is including regulatory support of Clinical Trials, New Chemical Entity’s development (NCE), Marketing products, Generics and Medical devices.
At ProRelix Research, our prominent expertize provide transparent and efficient services in drug development programs which include regulatory support of clinical trial, new chemical entity’s development (NCE), marketing products, generics and medical devices in India, USA, Europe, UK
