Doing Business Responsibly
Society has increasingly high expectations for ethical behavior from global healthcare companies – expectations that very often go beyond what is legally required. We are taking steps to ensure our standards align with these expectations.
In Lek, a Sandoz company, we were among the first companies to accede to the Slovenian Corporate Integrity Guidelines. We have become the ambassador of Corporate Integrity as we consider it of essential importance for conducting responsible business practice and achieving sustainable development.
Therefore, integrity as a shared Novartis value guides us in our decision-making processes.
Our good business practices, ethical conduct and legal compliance are based on the principles of the Novartis Code of Ethics.
We recognize the interests of our stakeholders and are building long-term relationships using different kinds of collaboration. Listening and seeking answers to questions are the basic principles of dialog and inclusion.
Our key stakeholder groups are our patients, our healthcare partners, our associates, local communities and regulators.
At the heart of the business strategy
Corporate responsibility is endorsed and ingrained at the highest level in our company. It is the integral part of our business strategy. We pursue it with all our business activities, functions, and our stakeholders.
Long term and annual goals have been set regarding all corporate responsibility aspects and we are taking measures for their implementation.
Prudence and sustainability go hand in hand with environmental impacts
Responsible business conduct is directly linked to the environmental responsibility, which is yet another primary interest of our associates and local communities. Lek, a Sandoz company, aims at providing good environmental practices in all phases of the production process and the life cycle of our products.
Strict compliance with pharmacopoeia and other requirements
The development and manufacture of medicinal products strictly comply with Pharmacopoeia requirements, WHO and OECD standards; requirements of the FDA and the Public Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (JAZMP), and the Good Laboratory Practice recommendations.
The development of medicinal products, APIs and manufacturing procedures is based on precautionary measures such as progressivity, inclusion of independent scientists, as well as open and transparent consideration of strengths and weaknesses.