Quality and products features
The quality and safety of our products are of utmost importance to ODS. The company’s quality systems are constantly kept up-to-date with the evolution of regulatory requirements and clients’ needs. Every team member of ODS Pharma is committed to maintaining quality at its top priority.
Based on the latest guidelines, an effective pharmaceutical quality system is implemented in ODS Pharma to ensure compliance with cGMPs by focusing on:
Evaluation analysis and quality risk management tools
We focus on the development, manufacture and sale of quality generic medications, and by offering high-quality, lower-cost alternatives to proprietary medications, we’re striving to reduce the overall costs of healthcare. With a quality system at the center of our operations and by providing a state-of-the-art supply chain, our products are differentiated by Effectiveness, Affordability, Having a low level of side effects, Reliability, Availability, and Safety from similar products in the market.
We strive to convert scientific innovation into hope and solutions for patients. Our deep customer relationships, quality medicines and consistently delivered promise make us a trusted brand.
Pharmacovigilance involves identifying, quantifying, assessing and preventing risks associated with the use of drugs that are already on the market. The aims are:
Earlier detection of as-yet unknown adverse drug reactions and interactions
Identifying increasing frequency rates of known adverse drug reactions
Identifying and minimizing the risk factors of adverse reactions, and their possible underlying causes
Estimating the quantitative aspects of the benefit/risk balance of drugs, and diffusing that information to improve regulation and rates of prescription
As a marketing authorization holder, ODS Pharma has an obligation in law for Pharmacovigilance implementation. A number of tools and processes are used to fulfill this obligation: