About Us

As the leading provider of specialized services for the pharmaceutical industries, compliance with customer satisfaction is our priority. ReClin Pharma Services (RPS) assists its clients for drug product life cycle management in alignment with country specific requirements, data generation for drug substance and drug product, document compilation (CTD or eCTD) as per regulatory standards for submission to various regulatory agencies all over the world, responding to the regulatory queries supporting product approval.

Our team has expertise in preparation and submission of dossiers for various regulated and semi-regulated markets e.g. U.S.A, Europe, Australia, New Zealand, Canada, Asia Pacific, CIS etc. We commit complete confidentiality in terms of handling each and every client requests. In order to cater to the requirement of our clients, RPS has well versed consultants overseas for any immediate clarification of regulatory requirements.

Another key expertise of RPS is to supply various analytical impurities and working standards as per various Pharmacopeia and in-house standards. RPS is committed to its clients for having complete transparency in day to day business transactions, timely deliveries of materials with highest business ethics. RPS has association with national and international drug intermediates & impurities manufacturers. Active communication with the drug manufacturers gives us a platform to commit our client a cost effective and timely solution of their requirements.

Thorough understanding of chemistry, analytical and regulatory aspects of various stages of drug development is the key differentiation from our close competitors. RPS not only works as supplier of material but actively provides support and consultancy in order to resolve any conflicts in terms of non-compliance of any specification parameters, purity issues or any other analytical troubleshooting. RPS works with the vision of becoming one stop service provider for pharmaceutical industries with respect to regulatory services, pharmaceutical intermediates, impurities, and working standards supplier and clinical trial/bioequivalence studies related services.

After an impeccable business journey and earned client’s trust, RPS has entered into a new vertical of clinical trial monitoring, medical writing and translation services. With more than 15 years of experience in CROs, our team takes care of these services in compliance with Good Clinical Practices and other applicable regulatory requirements.