Preclinical Support
Your Trustworthy Partner for Reliable, Evidence-based results, Ensuring Compliance and Quality at Every Step of your Preclinical Drug Development Journey
Your Trustworthy Partner for Reliable, Evidence-based results, Ensuring Compliance and Quality at Every Step of your Preclinical Drug Development Journey
We offer complete preclinical support services for biotechnology and pharmaceutical sectors, ensuring precise and legal research, providing reliable evidence for drug development choices, thanks to our advanced facilities and knowledgeable staff.
To ensure the safety and efficacy of your drug candidates, you need robust preclinical assistance as you navigate the path from discovery to clinical trials. With a broad range of studies and regulatory support, Zenovel’s Preclinical Support Services offer complete solutions that help your drug development projects go forward successfully.
Our team combines industry knowledge with IT proficiency to provide tailored solutions
for the specific challenges of the pharmaceutical sector.
Our innovative technology enhances operational efficiency and data management through cutting-edge solutions.
Offers comprehensive IT services, from system implementation to ongoing maintenance and support, ensuring seamless integration and operation of your IT infrastructure.
Our IT solutions are designed to be tailored
to your specific organization’s requirements,
ensuring optimal performance and
scalability.
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
