Drug Development and Discovery
Employing innovative solutions to accelerate drug discovery and development
Employing innovative solutions to accelerate drug discovery and development
Zenovel is dedicated to enhancing drug development and discovery by offering advanced solutions, addressing challenges, and bringing therapeutic ideas to fruition.
Drug research and discovery is an intricate field that involves knowledge, creativity, and accuracy. From original research to clinical development, Zenovel offers comprehensive services for every stage of the drug development process. Our comprehensive strategy guarantees that your medication/ drug candidates satisfy the highest requirements for efficacy, safety, and quality, and are optimised for success. We provide advanced drug development and discovery services, utilizing advanced technologies and a team of experienced scientists, to expedite the development of drug candidates, providing insights and support for innovative therapies.
Zenovel’s Chemistry Services provide comprehensive support in medicinal and synthetic
chemistry, enabling the development of innovative therapeutics from concept to clinic, leveraging the expertise and resources required for drug discovery and development.
Our team, comprising experts in chemistry, biology, pharmacology, and regulatory affairs, offers comprehensive support for drug development projects.
We utilize the latest technologies and methodologies to enhance innovation and efficiency in drug discovery and development.
Works closely with clients to create conducive environment that enhances project success and expedites development timelines.
We guarantee the highest quality and regulatory compliance, ensuring your products meet all safety and efficacy guidelines.
We offer tailored services to meet the unique needs of your projects, ensuring that your drug candidates are optimized for success.
The European Union’s Good Manufacturing Practice (GMP) standards, as outlined in the Annex to the Guide to Good Manufacturing Practice for Medicinal Products, ensure the quality and safety of medicinal products, including those used in clinical trials. The Qualified Person (QP) plays a crucial role in batch certification, particularly for
In the intricate process of developing new pharmaceuticals, guaranteeing product safety, effectiveness, and adherence to global regulations is essential. Batch release testing acts as a pivotal quality assurance measure, confirming that medications comply with rigorous criteria before distribution. When combined with International Council for Harmonisation (ICH) standards, this testing framework
In the world of life sciences, quality isn’t just a benchmark—it’s the backbone of success. Three key pillars—Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), and Good Laboratory Practice (GLP)—form the core framework that supports everything from product development to regulatory approval. These standards aren’t just industry buzzwords; they’re the
In the pharmaceutical industry, quality is paramount—and at Zenovel, we are deeply committed to delivering excellence in Quality Assurance (QA). Our focus is on ensuring that every medicine is developed, manufactured, and delivered with safety and reliability as top priorities. QA is embedded in every stage of the pharmaceutical lifecycle—from
The U.S. Food and Drug Administration (FDA) emphasize the importance of data integrity in pharmaceutical manufacturing, particularly under its Current Good Manufacturing Practices (CGMP) rules. However, issues like fake lab results and sloppy record-keeping persist, posing risks to patients and losing confidence in the system. Independent oversight is crucial to
In the rapidly evolving pharmaceutical industry, assuring product quality and customer safety is a need. This endeavour continues to be based on validation, a methodical procedure to verify that manufacturing procedures and equipment consistently deliver high-quality outcomes. A strong strategy to validation is required in 2025 due to the complexity
