Rudra marketing solutions is one of the reputed companies based in Ahmedabad (Gujarat, India) engaged in providing pharmaceutical regulatory services in India. We are supported by a team of experts who execute these services, according to the requirement of our worthy clients. We help the pharmaceutical companies stay one step ahead of regulatory changes, and upgrade their end-to-end regulatory activities. We provide services for good manufacturing practices (GMP), validation, training and documentation, drug master file (DMF), mock audits and many others, as per regulatory requirements. Widely acknowledged for efficiency, responsiveness, strategy and for being personalized, the services that we offer are one of the best in this industry. Get in touch with us to avail our pharmaceutical regulatory services at a budget-friendly price.
Some Key Facts about Our Technical Team & Working Module:
|Communication with MOH
|Preparation, Compilation & Review of 2.4 & 2.5 Module ((For Generic/Hybrid/Bibliographic application)
|Preparation, Compilation & Review of Risk Management Plan (RMP)
|Review of RTR (Refuse to receive standard) as per RTR Guideline
|Review of Dossier as per ANDA Checklist
|Review of BA/BE Study as per MOH Guideline
|Due Digilance of Dossier
|POST – APPROVAL
|Variation Filing / Supplement Filing
Rudra Marketing Solutions
F-43, City Square Mall, Godrej Garden City, Behind Nirma University Off Sarkhej, Gandhinagar Highway Village, Jagatpur, Ahmedabad, Gujarat - 382470, India
Mobile : +91-9377382001
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