The RLS Regulatory Affairs team has significant global experience in drug development and establishment of regulatory strateigies. This endows our clients to develop their new drugs more efficiently and to accomplish timely and successful regulatory submissions.
RLS is an association of regulatory affairs consultants, providing consultancy to Pharmaceutical and Active Pharmaceutical Ingredients (API) industries.
RLS expertise in development of Dossiers, Drug Master File (DMF), and Common Technical Document (CTD).
RLS provides regulatory affairs consultancy tailored to meet client’s specific needs. Client’s data security and confidentiality is assured to the highest level.
We provide services from submission to final approval at the office of DCG(I), FDA Bhawan, New Delhi. We facilitate the guidelines for getting approval / N.O.C. for following applications:
We have tie-ups with well established laboratories to carry out analytical testing (HPLC,LC-MS, GC-MS,IR,UV,X Ray Diffraction, DSC, NMR).
In short, we serve the entire spectrum of regulatory needs for our clients, based on experience and knowledge.
If you are a Study Sponsor, and you are interested in contacting us about a current or upcoming project or if you require any other assistance, please contact at : 91-11-49077601, 91-9873038019 / Email: contact@rahelife.com
