From a stable formulation to a compliant and up-to-date product specification. Marketing and maintaining a health product requires the necessary expertise.
Pannoc provides you with tailor-made guidance, in exactly those aspects where you want support.
Launching a health product responsibly requires navigating a strict and multidisciplinary regulatory process. Furthermore, maintaining an existing product demands continuous follow-up and exhaustive documentation in accordance with current requirements.
Pannoc guides you through every step: from initial formulation to the compilation of the regulatory dossier, including clinical test batches and stability studies in accordance with ICH guidelines.
Working with its partners, Pannoc assists you with new medicinal products, medical devices, and cosmetics.
Once on the market, every health product requires continuous follow-up in accordance with category-specific regulations. Pannoc acts as your dedicated partner in this, ensuring the conformity, quality, and safety of your product throughout its entire lifecycle.
Our expert R&D team and reliable partners work closely with customers to develop, refine and optimize formulas for semi-solid products, with attention to stability, efficacy and workability. In this phase, we can also carry out exploratory stability tests.
With a specialization in semi-solid products and more than 47 years of experience, we can help you with:
• new formulas
• creating innovative new product extensions
• reformulations
• reverse engineering
• ...
We guide you from preformulation to final formulation. Based on your feedback, we refine the formulation step by step until it fully meets your expectations.
Any new formula, regardless of category — cosmetic, medical device or drug — must be supported by a complete and compliant regulatory dossier. This dossier forms the backbone of every market introduction process and includes technical documentation, safety evaluations and the necessary substantiation of effectiveness and quality.
At Pannoc, we have the pharmaceutical expertise to guide this process from A to Z — from initial file structure to continuous follow-up after market introduction. Because an existing product also requires an up-to-date file, adapted to the ever-evolving regulations.
For regulatory records in medicines, medical devices and cosmetics, we work with carefully selected partners to prepare submissions, ensure regulatory compliance and accelerate time to market.
We specialise in technology transfer, ensuring that production processes developed at other locations are accurately and efficiently replicated at our premises. This allows Pannoc to seamlessly act as the new manufacturer of your product and, if necessary, the necessary validation batches will be perform for regulatory approval.
Our expertise also includes producing clinical trial samples, providing full support to ensure a smooth scaling up from development, through clinical trials, to full commercialization. Pannoc is fully equipped to produce clinical batches when necessary.
To ensure a smooth transition from formulation to GMP production, we offer extensive process development and analytical support. We specialize in optimizing mixing, emulsification, homogenization and dissolution techniques, as well as developing effective scaling strategies.
Pannoc has a fully equipped QA department for carrying out validations as part of the registration dossier — from preparing validation protocols to effective implementation after approval.
Pannoc offers comprehensive analytical services to evaluate the physico-chemical properties, stability and performance of your formulations. Our expertise includes the development and validation of analytical methods according to the ICH guidelines for pharmaceutical products, ensuring accuracy and precision.
Our Analytical Development team guides your product from concept to market launch, applying test methods that comply with international regulatory standards.
Our complete GLP-compliant internal QC team offers a wide range of services including:
Pannoc offers comprehensive stability tests to support your product development and regulatory requirements, including:
