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(ANVISA Approved & EU Approvable)

Sterile Lyophilized PPI’S, General Lyophilized API & Lyophilized Vials, Dry Powder Vials.

Our manufacturing facilities meet stringent cGMP norms, laid down in the "Revised Schedule M" by the Drug Controller (General) India, Ministry of Health, and Government of India.

WHO-GMP certifications of the Group's manufacturing facilities are testimony to its compliance with the World Health Organization’s international norms.


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