Intellect Pharma Consultancy
IPC is a trusted and fast-growing organization in the life sciences and pharmaceutical domain.
With over two decades of experience in Pharma-IT and Regulatory Assurance, we bring hands-on expertise in Computerized System Validation (CSV), regulatory compliance, project setup, and comprehensive pharmaceutical operations support.
Our team actively delivers country-specific regulatory services for the registration of Human Drug Products, APIs, Cosmetics, Dietary Supplements, Herbal Medicines, Veterinary Products, Excipients, and Primary Packaging Materials. We ensure that every submission aligns with applicable regulatory frameworks and authority expectations.
At IPC, we recognize the critical role regulatory authorities play in safeguarding public health. We work diligently to strengthen our clients’ compliance posture—protecting their reputation while ultimately contributing to patient safety and well-being.
We partner closely with our clients, providing strategic implementation support along with advanced technological (IT) solutions designed to meet evolving regulatory and business demands.
IPC also offers structured knowledge-transfer programs and professional training across key areas, including GMP requirements, 21 CFR Part 11, 21 CFR Part 58, 21 CFR Part 800, 21 CFR Part 820, QMS, ISO 9001:2015, ISO 13485, CTD and dossier submissions, Computerized System Validation, and regulatory documentation.
