Operations

We are a globally compliant, technically strong, and reliable pharmaceutical manufacturer

Manufacturing Facilities

As a WHO-GMP approved organization, we operate two world-class manufacturing units offering various sizes of tablets and capsules in the general category.
Designed by the renowned global consultancy IPS-Mehtalia, our state-of-the-art infrastructure fully adheres to EU PIC/s and cGMP standards.
Our facilities are engineered for global compliance, meeting the rigorous regulatory requirements of the US, EU, and other international markets.

Jay Formulations maintains an In-House Regulatory Affairs Division, comprised of a dedicated team of highly qualified pharmacists and regulatory specialists.
This team serves as the strategic backbone of our global operations, ensuring seamless market access through technical excellence and rigorous compliance.

QC is an independent unit and responsible to carry out the analysis of Raw Materials, Packaging Materials, In-Process samples and Finished Products, following ‘Data Integrity’ principles (ALCOA+).
QC unit meets Schedule ‘L1’ (Domestic standards for GLP Compliance of Laboratories) as well as any other International standards.
QC unit is supported by all sophisticated analytical instruments to ensure the complete In-house analysis of all the samples. QC instruments are in compliance with 21CFR Part 11.