Regulatory Consulting Services
AARIYA is adept in handling end-to-end market authorizations and product life-cycle management of all major HAs.
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Regulatory Consulting Services
At AARIYA, we offer our clients highly professional and effective services to all of their Regulatory Affairs requirements. Our experts are adept in handling end-to-end market authorizations and product life-cycle management of all major HAs like, the United States Food and Drug Administration (US FDA), the European Medicines Agency (EMA), the European Directorate for the Quality of Medicines (EDQM), the Therapeutic Products Directorate (TPD), the Pharmaceuticals and Medical Devices Agency (PMDA), the Therapeutic Goods Administration (TGA), the New Zealand Medicines and Medical Devices Safety Authority (Medsafe), the South African Health Products Regulatory Authority (SAHPRA), Ministry of Health (MoH) of Russia, Latin America (LATAM), Middle East and North Africa (MENA), Asia Pacific (APAC), Association of Southeast Asian Nations (ASEAN), Commonwealth of Independent States (CIS) regions, and the World Health Organization (WHO).
Regulatory Strategy:
Without sufficient understanding on right Regulatory strategy, many companies face delays in product registration that affect the costs... Read More
Regulatory Operations – Chemistry, Manufacturing and Controls (CMC):
Whatever your product, no pharmaceutical regulatory affairs consultancy knows the CMC process better than AARIYA... Read More
Regulatory Intelligence:
Staying current with the ever-changing regulatory landscape is challenging. New changes emerge almost every day, and a lack of harmonization across all the regions you work in only adds to the complexity... Read More