Our Services

We provide end-to-end consulting and execution support for setting up pharmaceutical and nutraceutical manufacturing plants in compliance with national and international regulatory standards. Our expertise ensures smooth project execution from concept to commercialization while meeting all statutory requirements

Our Services


Plant Setup & Validation

We Provide complete Plant Setup & Validation from Greenfield & brownfield project planning to Documentation & SOP preparation. Facility design (GMP), Installation, Operational, Performance Qualification to Process & cleaning validation, Documentation & SOP preparation.


HVAC System Design & Validation

We Provide complete Design of HVAC systems, Airflow pattern studies & pressure differential management, Temperature & humidity control systems, Validation of HVAC performance & cleanroom classification, Energy-efficient system optimization.


Man & Material Movement Planning

We Provide complete Layout design ensuring unidirectional flow, Cross-contamination prevention strategies, Personnel and material entry/exit protocols, Cleanroom zoning and segregation, Workflow optimization for regulatory compliance for Man & Material Movement Planning.


Licensing & Regulatory Approvals & Regulatory Affairs

We assist in obtaining and renewing licenses from key regulatory bodies such as Drug manufacturing licenses, Nutraceutical/Food licenses, Import-export licenses, State and central regulatory approvals & all types of regulatory affairs.


Medical devices

We Provide complete end to end support for procuring Medical devices required for setup. We also do SOP preparation. Facility design, Installation, Operational, Performance Qualification to Process & cleaning validation, Documentation and SOP preparation for medical devices. We can also help in identifying right source for procurement.


Indian FDA query

We provide Indian FDA query services that help verify and manage Drug, Cosmetic, Medical Device, and Food licences. Maharashtra FDA provides online regulatory services, while CDSCO/ONDLS supports drug licence verification. For food licences, use FSSAI FoSCoS to apply, track, renew, verify licences, and raise complaints.


CDMO/CMO assistance

We provide end-to-end support for pharmaceutical development and manufacturing, including product formulation, process development, regulatory compliance, quality assurance, production, packaging, and technology transfer. These services help companies reduce costs, accelerate market launch, and ensure efficient, reliable product manufacturing.


Licensing Formulation Development Compliance

We provide support pharmaceutical companies with regulatory approvals, product development, documentation, quality standards, and legal requirements. These services ensure smooth licensing processes, efficient formulations, and compliance with industry regulations for successful product commercialization.


Pharmaceutical Pellets & Granules

Pharmaceutical Pellets and Granules are solid oral dosage forms widely used in drug manufacturing to improve drug delivery, stability, and patient compliance.


Pharmaceutical Excipients

Pharmaceutical Excipients are the inactive substances formulated alongside the API in a medication. Excipients play a crucial role in medicine.


Cosmetic Grade Excipients

Cosmetic Grade Excipients are inactive substances used in cosmetic and personal care formulations. They act as carriers, stabilizers, or functional additives.


Natural Extract

Natural Extract refers to a biologically active substance obtained from natural sources such as plants, herbs, marine organisms, or microorganisms. Used as a raw material.

Why Us?