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Sark Pharma Headquarters

Sark Pharma Tech Services

Your trusted digital platform for pharmaceutical compliance, SOP management, and regulatory intelligence.

Our Mission

Sark Pharma Tech Services was built to bridge the gap between the complexity of pharmaceutical regulations and the day-to-day operations of quality professionals. We provide structured, editable, and professionally authored Standard Operating Procedures (SOPs) that help pharmaceutical manufacturers, research labs, and regulatory teams stay audit-ready and compliant at all times.

  • Support pharma professionals with ready-to-use GMP-compliant documentation
  • Improve GMP compliance across pharmaceutical manufacturing facilities
  • Provide ready-to-use, editable SOPs and regulatory templates
  • Deliver affordable access to pharmaceutical knowledge for organisations of all sizes

Our Vision

To become the world's most trusted and comprehensive pharmaceutical knowledge platform — empowering every GMP facility, from emerging startups to global manufacturers, with the documentation, education, and regulatory intelligence they need to operate at the highest standards of quality.

Founder & Leadership

RS

SARK Pharma limited

Founder, Pharmaceutical Quality & Compliance Expert

With over a decade of hands-on experience in the pharmaceutical industry, our founder has worked across Quality Assurance, Quality Control, Regulatory Affairs, and Production departments in licensed pharmaceutical manufacturing facilities.

Experience

17+ Years in Pharma

Qualification

M.Pharm / Pharma Sciences

Expertise

QA, QC, Regulatory, GMP

Areas of Expertise

QAQCRegulatory AffairsProductionITSHEPharmacovigilanceWarehousesHR & AdminPackaging DevelopmentFormulation & DevTechnology TransferEngineering

What We Offer

SOP Database

Professionally authored, MS Word-editable SOPs covering QA, QC, Microbiology, Production, Regulatory Affairs, and more.

SOP Library

Free access to the written content of our SOPs — browse, read, and understand procedures before purchasing.

Regulatory Insights

Curated articles and expert commentary on FDA, EMA, WHO, and ICH guidelines to keep your team informed.

Compliance-Ready Templates

All documents are structured to meet GMP, GLP, GDP, and cGMP requirements, ready to be customised for your facility.

Industries We Serve

Pharmaceutical ManufacturingBiotechnologyMedical DevicesResearch & DevelopmentClinical LaboratoriesContract Research OrganisationsNutraceuticalsVeterinary Pharma

Get in Touch

Custom SOP requirements, bulk licensing enquiries, or general questions — we're here to help.

Location

Maharashtra, India

Response Time

We typically respond within 1–2 business days. For urgent SOP requests, please mention "URGENT" in your subject line.