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


Our Client’s Testimonials

    Manager-Regulatory AffairsHead of Regulatory Affairs
  • Aariya’s seamless support in arranging quality labeling, technical inputs, quality review, and most importantly their short turn-around time helped us in timely response to the FDA thereby assisting in securing faster product approval.
    Manager-Regulatory Affairs
    A Malaysian Based Generic Pharmaceutical Company
  • They are great with their prices and excellent with their turn-around times. The most important quality that I like about Sachin and his team is that they would go that extra mile to get the job done and have so far never let us down.
    Head of Regulatory Affairs
    A US Based Generic Pharmaceutical start-up