Regulatory Affairs
Amvish Pharma’s in-house regulatory team includes experts in global regulatory requirements in submitting ACTD, CTD, eCTD and Country specific dossier and documents across US-FDA, Health Canada, and Rest of the World (RoW) markets. We provide ACTD, CTD, eCTD, NeeS and country-specific dossiers to ensure smooth market access for our products.
Our team ensures compliance with international standards, guaranteeing all products meet the highest safety and quality requirements. With their expertise, Amvish Pharma delivers trusted healthcare solutions globally, supporting healthier lives.
Ensuring Global Compliance and Quality in Healthcare Solutions
Expertise in Global Regulatory Requirements
Amvish Pharma's regulatory team possesses in-depth knowledge of global regulatory standards, particularly for US-FDA, Health Canada, and Rest of the World (RoW) markets.
Commitment to Quality and Safety
The regulatory team at Amvish Pharma is dedicated to maintaining the highest quality and safety standards for all products.
Supporting Healthier Lives Globally
Through comprehensive regulatory compliance and expertise, Amvish Pharma extends its trusted healthcare solutions across the globe.
