Are you looking for a manufacturer for a new health product, or do you want to change manufacturers?
As a CDMO, we are happy to support you.
As one of the leading pharmaceutical Contract manufacturing manufacturers in Belgium, we focus exclusively on the production of semi-solid products. Pannoc has built up decades of experience and in-depth technical expertise as a recognized market leader in the production of ointment bases for magisterial preparations. We use this expertise in the development and production of semi-solid formulas.
No tablets, no liquids. We are all about semi-solid products.
We maintain a strict quality assurance at every stage of the production process and use advanced equipment and methods that comply with international regulatory standards, including those of the EMA and GMP.
Once the dossier for your pharmaceutical product, medical device or health product has been approved, we are ready to produce for you. We take care of every phase of the production process on your behalf, minimizing lead times and allowing rapid market introduction.
At Pannoc, your creams, gels, lotions and other semi-solid products are in the hands of an expert.
We offer flexible batch sizes, from small-scale clinical production to full commercial production. This way, we can meet a variety of project requirements. Our facility is fully compliant with Good Manufacturing Practice (GMP) standards. This allows us to meet the highest quality requirements.
We offer a wide range of packaging solutions designed to meet both regulatory and commercial objectives. This includes primary packaging that protects product integrity and secondary packaging that increases product visibility and appeal.
The release of finished products is carried out under strict regulations and quality standards to ensure patient safety and product integrity.
Drugs are released by a Qualified Person (QP), raw materials/compounding creams by the Responsible Pharmacist (RP), and other products supervised by our department Quality Assurance (QA). All release decisions are made by independent staff who are not involved in production, ensuring objectivity and regulatory compliance.
Prior to release, batch documents are thoroughly reviewed, all in-process controls are verified, and internal QC analyses are accurately performed in our laboratory. Each step of the process is documented and reviewed to ensure full compliance with applicable regulations and internal quality standards.
Pannoc has its own in-house laboratory, specialized in the development and release of medicines, medical devices and health products. Because all phases are carried out internally, including microbiological tests, Pannoc maintains full control over the processes and guarantees a faster and more efficient product release.
Pannoc's fully equipped internal laboratory offers comprehensive quality controls to ensure the safety, efficacy and consistency of all products. These include:
Our Quality Assurance team ensures that all products and processes meet the highest regulatory and quality standards.
We are fully committed to providing products that are 100% safe and consistently of the highest quality. Only the highest quality is good enough for Pannoc.
Our site is regularly inspected by the Belgian authorities (Federal Agency for Medicines and Health Products — FAMHP), as well as by our customers.
