Pharma Regulatory Affairs Services/ DossierSpark Pharma Regulatory Consutant
- Regulatory affairs
We, Spark Pharma regulatory consultant is an India based Pharmaceutical Regulatory consultant, Located in Ahmadabad, Gujarat, India. Spark Pharma regulatory consultant is involved in a wide variety of regulatory consulting assignments which Regulated markets e.g. U.S.A, Europe, Canada, Australia etc. and Less regulated markets e.g. India, Asia Pacific, CIS, Middle- East, Africa etc.
Spark Pharma regulatory consultant assist clients by guiding the product development in line with the country specific requirements, data generation, document compilation for submission to various Regulatory Agencies all over the world, responding to the queries and finally obtaining the approval or registration of the product all under one roof.
Our core focus is to offer supportive services to Regulatory Departments of Pharmaceutical Companies in the field of Registering Pharmaceutical Dossier Writing. We are have been involved with all aspects of regulatory affairs, from supporting Clinical trials, bio-equivalence reports, validation data, Expert reports, Data for Overview, PSUR through registration activities, compilation of Pharmaceutical dossier / application for registrations of medicines and E-Filings to post-marketing regulatory obligations for Pharma Industry.