Our Services

Quality Management

Our quality management services are designed to guarantee that all pharmaceutical processes meet stringent quality standards, ensuring the safety and efficacy of products.

Approvals/Inspection

Our team provides expert support in obtaining approvals and handling inspections to facilitate the market entry of pharmaceutical products.

Third-Party Audits

Third-party audits are essential for ensuring regulatory compliance and practices. These evaluations identify risks, inefficiencies, and areas for improvement. Engaging external auditors provides impartial insights, enhancing operational integrity and leading to safer products.

USFDA - GMP/GLP Audits

These audits assess compliance with regulatory requirements, focusing on processes, facilities, and documentation. By maintaining rigorous oversight, the FDA helps protect public and ensures that companies adhere to the highest standards in their manufacturing and laboratory practices.

Regulatory

We assist in navigating complex regulatory requirements, ensuring compliance with all regulations to bring pharmaceutical products to market smoothly.

Training

We provide tailored programs on GMP to enhance skills and boost productivity. Our expert instructors and flexible delivery empower organizations to achieve their goals efficiently. us to stay ahead in today's competitive landscape.

PIC/S, EU - GMP/GLP Audits

These practices minimize risks involved in production, safeguarding both the consumer and the integrity of the product. Adhering to GMP guidelines is essential for compliance with regulatory requirements.

CRO Services

Contract Research Organizations (CROs) provides outsourced research services to companies. CROs enable pharmaceutical companies to focus on drug development while improving the overall quality speed of research processes.