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 pre-formulation 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.
India is a significant player in the global pharmaceuticals sector, characterized by a diverse population and cost-effective infrastructure. However, its potential in clinical research is hindered by complex regulatory challenges that delay innovations and deter investment, affecting the timely market introduction of life-saving drugs. This blog discusses the major obstacles
The FDA issued 466 Form 483s to drug organizations in FY 2022, more than double the previous year, highlighting significant quality failures in the pharmaceutical sector. For startups and scale-ups seeking market approval, the excitement of innovation often conflicts with the strict requirements of current good manufacturing practices (cGMP). Although
In the pharmaceutical and biotechnology industries, obtaining regulatory approval is essential prior to introducing new drugs or biologics to the market. A pivotal aspect of this approval process is the FDA Pre-Approval Inspection (PAI), which involves a comprehensive assessment of manufacturing facilities, processes, and data integrity to ensure adherence to
Risk Based Monitoring (RBM) is a more efficient alternative to traditional clinical trials, focusing on high-risk areas through data-driven insights. It ensures patient safety, data integrity, and regulatory compliance while reducing costs and timelines. However, the success of RBM depends on the competency of monitors, who identify risks, analyze data,
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 Certification) is
We provide affordable, innovative, and high-quality solutions to pharma industry with ethics driven research and increasing accessibility to high quality medicine worldwide
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