Vee Excel Drugs and Pharmaceuticals (VXL) stands as a prominent manufacturer and exporter of diverse healthcare items. Established in 2001 , the company initially focused on pharmaceutical products for the global market. Over time, recognizing the need to cater to various client demands in one place, the company expanded its offerings to include Nutraceutical and Ayurvedic products and later introduced a Veterinary division. Today, the company is renowned for its unwavering commitment to upholding quality standards. Our advanced manufacturing facility, spanning 5454 square meters, adheres to European guidelines and strictly complies with regulatory standards such as EU-GMP, MHRA and PIC/S. It features separate Beta-lactam (Cephalosporin) and Non-Betalactam sections. Additionally, the facility boasts a dedicated R&D center and a Testing Lab to ensure the products meet the highest international quality benchmarks. As a result, we have established a strong presence in more than 30 countries across AFRICA/ASIA/LATAM/CIS regions. Presently, VXL employs around 200 professionals who bring their expertise, dynamism, experience, and technical know-how to the team. Each member works collaboratively toward the organization's overarching objectives, contributing to the company's successful entry into new markets and expansion of its customer base.
In the dynamic world of healthcare , innovation in manufacturing plays a pivotal role. VXL stands tall as a beacon of progress, seamlessly managing three distinct manufacturing verticals: Pharmaceutical FDF's, Nutraceuticals and Veterinary Feed Supplements With a commitment to quality, integrity, and advancement, our company is at the forefront of providing essential solutions for human and animal well-being.
VXL operates across diverse business segments, each contributing to its operations -
Countries
Years Of Experience
Ready Dossiers
FDFs
1) Contract manufacturing of finished pharmaceuticals, nutraceuticals and veterinary feed supplement products 2) In Licensing and Out Licensing of products 3) Technology transfer projects
Our Quality Assurance Department (QAD) comprises a skilled and seasoned team that operates around the clock to ensure the utmost quality of our products. From raw materials to the final goods, we also handle post-market input to guarantee customer satisfaction. In order to manage this extensive workload effectively, we have divided the Quality Assurance process into distinct sections: Quality Control, Quality Surveillance, Validation, and In-Process-Control (IPC). These segments rigorously adhere to cGMP guidelines to align with international regulatory standards such as US-FDA, UK-MHRA, TGA-Australia, EU, and others. CAPA Tracking, Change Control, Market Complaints, Deviation management, Vendor qualification, Audit management, OOS/OOT and Document management alongside powerful automation with intelligent tracking are some of the modules we have incorporated via our pre-configured Integrated Quality Management System (QMS)
Customized handling of each inquiry and accurate pricing Utmost confidentiality Expert customer service Exceptional products at competitive rates A quality assurance system that aligns with cGMP stipulations Cutting-edge QC and F&D laboratories Procurement from authorized suppliers