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- Home Page
- Services
- Medicinal Products
- Regulatory Affairs
- Global Health Authorities-Specific Services
- Food and Drug Administration (FDA)
- European Authorities (EU)
- Active Substance Master File (ASMF)
- Centralized Procedure (CP)
- Certification of Suitability (CEP)
- Decentralized Procedure (DCP)
- Investigational Medicinal Product Dossier (IMPD)
- Mutual Recognition Procedure (MRP)
- National Procedure (NP)
- Lifecycle Management
- Regulatory Strategy Consulting Services
- Clinical Trials Regulation (CTR)
- Clinical Trial Application (CTA)
- Health Canada
- Drug Development Regulatory Services
- Regulatory Strategy and Insights
- Dossier Authoring Services
- Post-Approval/Lifecycle Management
- Country-Specific Regulatory Services
- Market Access with end-to-end Regulatory Solutions
- Global Health Authorities-Specific Services
- Regulatory Operations
- Regulatory Medical Writing
- Regulatory Pharmacovigilance
- Compliance, Audit, and Validation Services
- Regulatory Affairs
- Medical Devices
- Medicinal Products
- Insights/Resources
- Company
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X Pharma Plus Pvt. Ltd. is a global, knowledge-driven company providing end-to-end solutions in GMP compliance, regulatory affairs, clinical research, and operational excellence. With a team of subject matter experts across multiple domains, we deliver tailored services from audits and validation to pharmacovigilance, R&D, and contract manufacturing, ensuring clients meet global standards efficiently.
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