Simpruv offer comprehensive product development services to help the customer address complex drug development challenges and bring more products to the market faster in Nutraceuticals and Pharmaceuticals
Simpruv can help your company formulate development strategies for pharmaceutical and medical products, ranging from lead candidate selection to final regulatory submissions and post-market activities.
Our global perspective and scientific expertise will ensure success by adding efficiency and manageability to your development program.
Simpruv Pharmaceutical Product Development Services:
Comprehensive product development strategies meeting international standards, focusing on regulatory and toxicology requirements.
Preparation, review, management and filing of submissions worldwide in Common Technical Document (CTD/eCTD) format.
Scientific writing of nonclinical data (safety), clinical data, and preparation of CMC documents.
Compliance activities, including development of compliance programs and conduct of facility audits for adherence to GLP and GMP standards