A WHO-GMP Certified Company

Regulatory Service

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Regulatory Service

Navigating international regulatory requirements is complex, and our Drug Regulatory Affairs (DRA) consultants help companies plan and manage their pharmaceutical and medical product development programs. We provide services that ease the approval process for your products, ensuring swift market entry.

Our Regulatory Service Include

DMF (CTD format) Preparation, Review and Submission
Dossier Writing and Review
Dossier Registration
COA, COPP
Notarization

Our Regulatory Service Include

Drug Product DMF
Development & Preparation of documents
Content creation and document services

Pharmlite Pharmaceuticals LLP, a distinguished name in the Pharmaceutical & Healthcare Industry. Situated in Vadodara, Gujarat, India.

Regulatory Service

Our Regulatory Service Include

Our Regulatory Service Include

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