Our team's extensive experience and successful track record in global pharmaceutical regulatory affairs ensures your products meet all required standards and approvals.
We take the time to deeply understand your specific regulatory challenges and develop customized strategies to efficiently navigate complex requirements.
Poorvith Pharma is dedicated to upholding the highest levels of quality and regulatory compliance, giving you peace of mind throughout the product lifecycle.
ABOUT US
Poorvith Pharma offers a comprehensive range of regulatory and compliance
services to support pharmaceutical companies globally. Our expertise includes dossier preparation,
submissions, toxicology assessments, technology transfer and more. With a focus on quality and
regulatory compliance, we help clients navigate complex requirements and successfully bring products
to market. From WHO-GMP to PICS to EUGMP to USFDA, our team ensures the necessary approvals and
standards are met every step of the way.
Our mission is to be a trusted partner in the pharmaceutical industry, leveraging our extensive
knowledge and expertise to provide tailored solutions that drive success for our clients.
Our Services
Comprehensive regulatory, technical, and toxicology services for pharmaceutical, medical device, and cosmetic companies worldwide.
Fill out the form to connect with our regulatory affairs experts. We'll review your needs and provide customized guidance to navigate the complexities of global pharmaceutical regulations.
