Formulation and Analytical Services
Elevate Your Drug Development, Ensure Safety and Efficacy through Expert Analytical Methods
Elevate Your Drug Development, Ensure Safety and Efficacy through Expert Analytical Methods
We provide comprehensive formulation and analytical services for drug development, utilizing advanced facilities and an experienced team to ensure efficient product development for clinical trials and commercial production.
Zenovel provides a comprehensive range of services, including the creation of injectables, solid and liquid dosage forms, and other advanced formulations, ensuring the highest standards of quality, safety, and efficacy in pharmaceutical goods, from preformulation studies to stability testing.
Offers comprehensive support throughout the entire drug development process, from preformulation studies to final product testing.
We guarantee the highest standards of quality and regulatory compliance, ensuring your products meet all safety and efficacy guidelines.
Our team of formulation scientists is skilled in creating various dosage forms to ensure optimal drug product delivery and performance.
Our services are customized to meet your specific project needs, providing flexible and innovative solutions.
We guarantee the highest standards of quality and regulatory compliance, ensuring your products meet all safety and efficacy guidelines.
We offer advanced analytical laboratories utilize the latest technologies to provide precise and reliable testing results.
Welcome to the Zenovel Blog! We are a leading provider of drug regulatory consulting and education, focusing on advancing pharmaceutical innovation while ensuring safety and compliance. This blog delves into the essentials of Drug Regulatory Affairs (DRA), covering its scope, career opportunities, and intricate processes involved in bringing new drugs
The international pharmaceutical landscape is inherently connected to the global economy and global trade, which is consisted with the quality and safety assurance , well-controlled quality and safety. Compliance with international pharmaceutical standards has changed from an optional step to a requirement. The Pharmaceutical Inspection Co-operation Scheme (PIC/S) is the
Lipinski’s Rule of 5 (Ro5) is a crucial guideline in pharmaceutical development, helping researchers evaluate a compound’s likelihood of becoming an effective oral drug. However, with the rapid evolution of therapeutic strategies, it’s worth considering the relevance of Ro5 in the current drug design landscape. Understanding Lipinski’s Rule of 5
Regulatory affairs (RA) play a crucial role in the pharmaceutical industry; ensuring products meet quality, safety, and efficacy. As the industry grow further the need for qualified professionals to bridge gaps between companies and regulators increases. This blog explores Zenovel regulatory affairs expertise, our various facets, and valuable contribution to
Navigating the world of pharmaceuticals, medical devices, and biotechnology is never straightforward. With the diversity of regulatory compliance governs the Code of Federal Regulations (CFR) – a regulatory path that shapes companies’ efforts and implements how companies long for their products to be developed, manufactured, and marketed. For companies trying
The race to deliver life-saving therapies to patients is increasingly faster and more complex. Pharmaceutical and biotech companies are faced with a dizzying list of challenges — global clinical trials, continuously changing regulations, multiple complicated therapeutic areas, and pressure to innovate. This is where Contract Research Organizations (CRO) come in:
