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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.

|Job offer: Africa vs. America: Where can you save more|

Good Manufacturing Practices Explained simply |GMP |Quality standards |GMP training in 15 min

ISO in pharma |ISO 9001 |ISO 13485 |ISO15378 |ISO17025 |ISO27001 |ISO14001|ISO50001|ISO45001

Self-inspection in pharmaceuticals |Internal Audit |Regulatory Audit |GMP compliance |QMS System

Pharma equipment & working principles |Rapid Mixer Granulator |Fludized bed dryer |Multimil |Sifter

Fluidized bed dryer principle |FBD |Drying |product container

Tablet defects at the compression stage in pharmaceuticals

Rapid Mixer Granulator (RMG) |working, parts, utilities, MOC, Application

How to calculate product manufacturing costs at any industry

PAMRA Medicinal Product Registration Process for Tablets | Step-by-Step Guide for Malawi 🇲🇼

USFDA Product Registration Flow

ZAMRA Product Registration Process | Step-by-Step Guide for Zambia"

TMDA Medicinal Product Registration Process for Tablets | Step-by-Step Guide for Tanzania

|ALCOA+++ |Importance of ALCOA++ in pharmaceuticals |data integrity |Documentation

CAPA Explained: Correction, Corrective Action & Preventive Action (In Hindi & English)

Assay on Anhydrous Explained |Step-by-Step Guide |What is Assay on Anhydrous basis |Easy Explanation

Assay on Dried Basis Explained |Step-by-Step Guide |What is Assay on Dried Basis? | Easy Explanation

Assay on As Is Basis Explained |Step-by-Step Guide |What is Assay on As Is Basis? | Easy Explanation

List of Regulatory Authorities in the globe, USFDA, TGA, TMDA, PAMRA, ZAMRA, MHRA, EMA, CDESCO, PMDA