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The content, SOPs, templates, regulatory articles, and training materials provided by Sark Pharma Tech Services are intended for general informational and educational purposes only. Nothing on this website constitutes professional regulatory, legal, or medical advice.

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While every effort is made to ensure that documents are accurate, up-to-date, and aligned with current GMP, WHO, FDA, EMA, and ICH guidelines, Sark Pharma Tech Services does not guarantee that the use of any template or SOP will result in regulatory approval, audit clearance, or compliance with any specific authority.

All documents must be reviewed, validated, and approved by a qualified person within your organisation before implementation. Regulatory requirements vary by country, facility type, product category, and applicable regulatory authority.

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SOPs and templates provided are generic starting points designed to be adapted to your specific facility, processes, and regulatory jurisdiction. You are solely responsible for customising, validating, and implementing these documents in accordance with the applicable regulations that govern your operations.

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