New Drug Approval: Guidance for NDAs
Ved Pharma Consultancy offers comprehensive guidance for preparing and submitting New Drug Applications (NDAs) in compliance with CDSCO/DCGI standards. Our expert team assists with documentation, technical reviews, regulatory requirements, and query resolutions. We simplify the entire process, ensuring accuracy, efficiency, and timely approvals. Trust us to help you navigate the complexities of regulatory frameworks, bringing your innovative pharmaceutical products to market with confidence and ease.
IND/SND/FDC Approvals: Assistance in IND/SND/FDCs
Ved Pharma Consultancy provides expert assistance for obtaining approvals for Investigational New Drugs (IND), Subsequent New Drugs (SND), and Fixed Dose Combinations (FDC). Our team ensures compliance with CDSCO/DCGI guidelines, helping you navigate documentation, technical evaluations, and regulatory queries. From initial submissions to follow-ups, we streamline the process to secure timely approvals, enabling you to focus on innovation and product development while we handle the regulatory complexities.
Import & Export Services:
Ved Pharma Consultancy offers end-to-end assistance with import and export regulatory requirements, including import registration, export NOCs, dual-use NOCs, and test license NOCs. We ensure seamless compliance, enabling smooth international trade for pharmaceutical, cosmetic, and nutraceutical products.
- • Import Registration & Licensing
- • Export NOCs
- • Dual Use NOCs
- • NOCs for Test Licenses
Licensing & Renewals:
Ved Pharma Consultancy specializes in obtaining and renewing various licenses, including manufacturing licenses, registration certificates, and written confirmations. Our expert team ensures compliance with regulatory guidelines, streamlining the application and renewal processes. Trust us to handle the complexities, ensuring your operations remain compliant and uninterrupted.
- • Registration Certificate Renewal
- • Manufacturing Licenses
- • Written Confirmations
Special Codes: Neutral/Special Code NOCs.
Ved Pharma Consultancy provides dedicated support for obtaining Neutral and Special Code NOCs, ensuring seamless compliance with regulatory requirements. These codes are essential for specific product classifications, and our team handles the documentation, submission, and follow-ups with regulatory authorities. We simplify the process, ensuring accuracy and timely approvals, so your pharmaceutical, cosmetic, or nutraceutical products meet all necessary guidelines for distribution and market entry.
Medical Device Services:
We assist with licensing, clinical investigations, import/export registrations, and compliance for medical devices and in-vitro diagnostics (IVD).
- • MFG LIC -For commercial Purpose and For Test & Evaluation Purpose
- • Loan LIC- For Commercial Purpose
- • Import LIC- For commercial Purpose and For Test & Evaluation Purpose
- • Clinical Investigation for MD & IVD
- • Distribution /Wholesale LIC
- • Market Standing Certificate
Cosmetic Regulatory Services
Ved Pharma Consultancy offers expert assistance with cosmetic import registration and manufacturing approvals. We ensure compliance with regulatory standards, handle documentation, and streamline processes, enabling you to bring high-quality cosmetic products to market efficiently and hassle-free.
- • Import Registration
- • Manufacturing Approvals
Food & Nutraceutical Regulatory Services (FSSAI)
Ved Pharma Consultancy provides comprehensive support for obtaining FSSAI approvals for food and nutraceutical products. Our services include documentation preparation, regulatory compliance guidance, and assistance with licensing. We ensure your products meet safety and quality standards, streamlining the approval process to help you achieve timely market entry while adhering to all FSSAI regulations.
- • Comprehensive FSSAI Approvals
Additional Services:
- • Free Sale Certificates
- • Laboratory Testing Services
- • Bioavailability/Bioequivalence (BA/BE) Studies
- • Toxicity Studies & PK Studies
- • Quality Management System (QMS) Data Preparation
- • Dossier Preparation for Global Submissions
- • SUGAM Account Opening
- • NSWS Account Setup
- • Attestation Services
- • Global Clinical Trial Management
- • Plant Setup