Our teams offer a bespoke service.
- Comprehensive development of an analysis method to quantify a compound contained in an finished product.
- Adaptation of an existing method in case of product reformulation (change of form, excipients or industrial manufacturing process).
- Completion of product analyses during development (formulation) to verify the stability of the product over time.
Our GMP laboratory is equipped to carry out stability studies as part of your development projects or as post-marketing surveillance. Véto-pharma – Development and Manufacturing offers a large storage capacity within climatic chambers under ICH conditions for initial (real or accelerated time) or ongoing stability.
Storage and management of your samples:
- 25°C / 60 % HR
- 30°C / 65 % HR
- 40°C / 75 % HR
Storage under VICH conditions, surveillance 24 hours a day 7 days a week, in line with pharmaceutical requirements.
Consultancy on and completion of specific stability study protocols:
- Pre-stability for formula selection.
- Stability in long-term, intermediate and accelerated conditions.
- Stability after opening and in use.
- Ongoing stability.
- Container / content interaction.