SARK PHARMATECH SERVICES
SARK PharmaTech Services:
We Are SARK PharmaTech Services is a professional consultancy firm based in India works globally, dedicated to supporting pharmaceutical companies with high-quality documentation services. With a deep understanding of local and international regulatory requirements, we streamline your compliance journey. To be the most trusted documentation partner for pharmaceutical companies across globally.
✅ Pharmacovigilance (PV): Adverse Event Reporting Templates, PSURs / PADERs / DSURs, SOPs for PV Systems, Risk Management Plans (RMPs), Agreements (SDEA & TQA) and PV training module.
✅ Regulatory affairs (RA): CTD Dossiers (Module 1–5), International submission formats, Product Variation/Renewal, Product Information (PIL, SPC, Labeling), Regulatory Training Module.
✅ Quality Assurance (QA): SOPs, BMRs, BPRs prpearation, Audit & Inspection Readiness Documents, CAPA drafting, GMP Compliance Documents, Training module, Supplier Audits, F&D, and Product Trouble shoot.
SARK PHARMATECH SERVICES and Kavita Surana
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List of Regulatory Authorities in the globe, USFDA, TGA, TMDA, PAMRA, ZAMRA, MHRA, EMA, CDESCO, PMDA
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