Supply Chain & Warehousing

Sourcing Quality Materials
Our Supply Chain department ensures timely procurement of raw materials, packaging components, and essential supplies from qualified vendors, maintaining high standards and cost-efficiency.

Safe Storage & Material Control
This department manages the receiving, storage, and issuance of materials under controlled conditions. All materials are handled in accordance with GMP standards to ensure traceability and integrity.

Production Department

Precision in Manufacturing
Equipped with modern machinery and trained staff, our Production unit follows validated procedures to manufacture quality medicines. Every batch is produced under strict process controls.

Oral Solid Dosage (OSD) Forms

Handles the manufacturing of tablets, capsules, and powders in accordance with cGMP guidelines. Key processes include granulation, filling, compression, coating, and packaging. Focuses on non-sterile oral solid dosage forms.

Sterile Production (Injectables)

Responsible for aseptic manufacturing of liquid and dry injectables in cleanroom environments. Processes include mixing, filtration, filling, sealing, and sterilization, ensuring compliance with stringent international standards.

Quality Management System (QMS)

Wellborne’s Quality Management System (QMS) integrates both Quality Assurance and Quality Control to ensure consistent product excellence and regulatory compliance. It governs all processes, from development to final release, ensuring safety, efficacy, and continuous improvement.

Quality Assurance (QA)

Quality Control (QC)

Our Quality Assurance (QA) Department ensures that every product we manufacture meets the highest global standards of quality, safety, and efficacy. By strictly adhering to current Good Manufacturing Practices (cGMP) and fully complying with FDA, WHO, and ICH guidelines, we maintain robust systems and processes that safeguard patient health, uphold product integrity, and foster continuous improvement across all manufacturing stages

Our Quality Control (QC) Department ensures that every product consistently meets the highest standards of safety, purity, and potency. By adhering to Good Laboratory Practices (GLP) and complying with international regulatory requirements, such as those of the FDA, WHO, ICH, and various Pharmacopoeia guidelines, we conduct rigorous testing at every stage. Comprehensive documentation and meticulous analysis form the backbone of our processes, guaranteeing the reliability and integrity of our results.

Our Regulatory team manages product registrations, DRAP submissions, and dossier preparation. We ensure that every product meets the legal and technical requirements for market entry.

Regulatory Affairs

R&D (Research & Development)

Our R&D wing focuses on developing cost-effective, high-quality formulations. It supports product improvement, process optimization, and technology transfer.

Admin & Human Resource (HR)

This department handles staffing, employee welfare, training, and compliance with labor laws. We believe in a safe and empowering workplace for all our team members.

Responsible for the maintenance of HVAC, production machinery, and utility systems, this team ensures uninterrupted operations by maintaining optimal performance and safety.

Engineering & Maintenance