GxP services
With a commitment to excellence and compliance, we are your trusted partner in navigating the intricate compliance requirements of Clinical practises, Distribution practises, Laboratory practises and other aspects for the life sciences industry. We offer a comprehensive range of GLP services, including GLP audits, study monitoring, protocol development, and data management. Our GLP experts ensure that your laboratory facilities and procedures meet regulatory requirements, promoting the integrity and reliability of your data. Our GCP services encompass clinical trial management, site audits, investigator training, and regulatory submissions. We work closely with sponsors, investigators, and CROs to ensure that clinical trials are conducted ethically, scientifically, and in compliance with regulatory standards.
We provide GDP services to pharmaceutical manufacturers, wholesalers, and distributors, including GDP audits, temperature monitoring, and quality management. Our GDP solutions help ensure the integrity and quality of pharmaceutical products throughout the distribution chain, from manufacturing to delivery to the end-user.
EU GMP consultation
Oup assessment audits (Pre-inspection audit) which includes assessments of manufacturingr consulting services are tailored to meet the specific needs of each client, providing expert guidance on interpreting and implementing EU GMP regulations effectively. From gap analysis to strategy development, we help organizations navigate the complexities of EU GMP compliance. We conduct comprehensive ga facilities, processes, and quality systems to ensure compliance with EU GMP regulations. Our audits identify areas for improvement and provide actionable recommendations to enhance GMP compliance and product quality.
Pharmaceutical manufacturing plant set up/upgradation and Engineering
Privaan Health specializes in providing comprehensive solutions for pharmaceutical manufacturing plant set-up and engineering. With our expertise in pharmaceutical manufacturing processes and regulatory requirements, we offer end-to-end services to help companies establish state-of-the-art facilities that meet the highest standards of quality, compliance, and efficiency. Our team comprises experienced professionals with extensive knowledge of plant design and layout, equipment selection and installation, process validation, pharmaceutical engineering, regulatory compliance, and project management. We are committed to delivering innovative solutions that empower our clients to achieve their manufacturing goals effectively and efficiently.
Sounds relatable?
TALK TO OUR EXPERTS FOR AUDITS, GMP TRAINING, SOURCING SERVICES FOR YOUR BUSINESS.