Site Master File
Welcome to Pharmadocsline – your trusted source for Site Master File (SMF) documentation in the pharmaceutical industry!
We provide a professionally developed, fully GMP-compliant Site Master File template designed to meet global regulatory requirements, including WHO, EU GMP, and PIC/S guidelines. Our SMF template offers a structured and comprehensive overview of your pharmaceutical manufacturing facility—covering quality systems, infrastructure, equipment, personnel, validation, and documentation controls.
We provide a professionally developed, fully GMP-compliant Site Master File template designed to meet global regulatory requirements, including WHO, EU GMP, and PIC/S guidelines. Our SMF template offers a structured and comprehensive overview of your pharmaceutical manufacturing facility—covering quality systems, infrastructure, equipment, personnel, validation, and documentation controls.
Each document is delivered in fully editable MS Word format, allowing seamless customization to reflect your site-specific operations, systems, and compliance practices.
Whether you're preparing for regulatory inspections or simply updating your documentation, our Site Master File template helps you stay inspection-ready, save valuable time, and ensure your facility is accurately represented.
to gain instant access to a high-quality, audit-ready SMF that simplifies documentation and supports your GMP compliance journey.
| 1 | SITE MASTER FILE OF NEW COMPANY (XYZ PHARMA). |
| 2 | SITE MASTER FILE OF ALREADY RUNNING COMPANY (XYZ PHARMA) |
Note: Documents will be updated soon, if you need any document, you can contact on
WhatsApp No: +923355521621
Email: pharmadocsline@gmail.com
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