Stability Study Services – Guyana

Stability Protocol Preparation (GA-FDA Aligned)

• Long-term, accelerated & intermediate stability study design

• Climatic Zone IVb conditions (30°C / 75% RH)

• Batch selection, pull points & acceptance criteria

• Finished dosage forms, APIs, cosmetics & nutraceuticals

• Compliance with ICH Q1 series, WHO TRS & GA-FDA guidance

Stability Report Preparation

• GA-FDA–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

GA-FDA Regulatory Query Handling

• Stability-related deficiency response drafting

• Shelf-life revision & scientific justification

• Support during GA-FDA 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 Guyana?

• Experience with Guyana GA-FDA submissions

• ICH & WHO-aligned stability documentation

• Inspection-ready, authority-acceptable outputs

• Reduced regulatory observations and faster approvals

• End-to-end stability documentation lifecycle support