Stability Study Services – Turkmenistan
Stability Protocol Preparation (MoH Aligned)
Long-term, accelerated & intermediate stability study design
Climatic zone–appropriate storage conditions (hot / arid climate considerations)
Batch selection, pull points & acceptance criteria
Finished dosage forms, APIs, cosmetics & nutraceuticals
Compliance with ICH Q1 series, WHO TRS & national guidance
Stability Report Preparation
MoH-ready stability study reports
Clear tabulation and scientific evaluation of stability data
Shelf-life / retest period justification
OOS / OOT assessment and conclusions
Suitable for new registration, renewal & post-approval variations
Graphical Trend Analysis
Assay, impurities, dissolution & physical attribute trending
Early identification of OOT trends
Batch-to-batch comparison
Authority-friendly graphs with concise interpretations
MoH Regulatory Query Handling
Stability-related deficiency response drafting
Shelf-life revision & scientific justification
Support during MoH queries, renewals & post-approval changes
Products Supported
Finished dosage forms (tablets, capsules, liquids, injectables, topicals)
APIs & intermediates
Cosmetics & personal care products
Nutraceuticals & herbal products
Why StabilityPro for Turkmenistan?
Experience with Turkmenistan MoH submissions
ICH & WHO-aligned stability documentation
Inspection-ready, authority-acceptable outputs
Reduced regulatory observations and faster approvals
End-to-end stability documentation lifecycle support
